WO2001057126A1

WO2001057126A1 - Candle wax stabilized by a combination of uv absorber plus a selected hindered amine

Info

Publication number: WO2001057126A1
Application number: PCT/EP2001/000681
Authority: WO
Inventors: James Lee Hyun; Walid Al-Akhdar; Kevin Trainor; Ramanathan Ravichandran; Mervin Gale Wood; Andrea R. Smith
Original assignee: Ciba Specialty Chemicals Holding Inc.
Priority date: 2000-02-01
Filing date: 2001-01-23
Publication date: 2001-08-09
Also published as: CN1420907A; DE60105761T2; KR100732534B1; EP1252227A1; CN1250626C; JP2003522243A; BR0107978B1; MXPA02007432A; JP4767470B2; CA2397713A1; BR0107978A; TW593670B; EP1252227B1; ATE277115T1; AU2001231687A1; US6221115B1; CA2397713C; KR20020070387A; DE60105761D1

Abstract

Candle wax containing a combination of a UV absorber, preferably a benzotriazole, in combination with a hindered amine which is substituted on the N-atom by an alkoxy, a cycloalkoxy or an hydroxy-substituted alkoxy moiety is surprising better stabilized than candle wax which contains a combination of a UV absorber and a conventional hindered amine where the N-atom is substituted by hydrogen or alkyl.

Description

Candle Wax Stabilized bv a Combination of UV Absorber Plus a Selected Hindered Amine

The instant invention pertains to compositions containing candle wax stabilized by a combination of a UV absorber, preferably a benzotriazole, plus a hindered amine substituted on the N-atom by an alkoxy, a cycloalkoxy or a hydroxy-substituted alkoxy moiety.

Candles have been known for many centuries going back to the eighth century B.C. The nature of candles is described in Ullmann's Encyclopedia of Industrial Chemistry, Volume A5 at pages 29-30 where it is seen that candles are made from paraffin, beeswax and stearin as basic materials, and where a host of additives may also be present.

It is not surprising that with candles and wax becoming increasingly more important attention was paid as to how to stabilize said materials. At the National Candle Association Meeting in Houston, 1994, R. van der Vennet presented a paper on "Antioxidants in Wax - Replacement of BHT" touting the use of Vitamin E (tocopherol) as an antioxidant to prevent the yellowing of wax when oxidized. WO 94/13736 describes the same invention.

EP 359,488 A3 and EP 133,964 B1 describe stabilized waxes used in cosmetics where the waxes are the same or similar to those used in candles.

EP 5,922 A1 describes lip cosmetics where the waxes are useful in lipsticks and are related to those useful in candles.

United States Patent No. 5,879,694 describes in detail transparent gel candles both in composition and structure. The use of BHT as an antioxidant is mentioned.

At the National Candle Association Technical Meeting on April 16, 1998, F. A. Ballentine et al., presented a paper entitled "Inhibiting Color Fading of Dyed Candles with CYASORB® Light Absorbers" in which the general theories of thermal oxidation and photodegradation are discussed along with data on the effect of light absorbers on color stability of dyed candle waxes. The light absorbers compared are 4-octyloxy-2-hydroxy- benzophenone UV-531; 4-methoxy-2-hydroxybenzophenone UV-9; 2-(2-hydroxy-5-methyl- phenyl)-2H-benzotriazole UV-5365; 2-(2-hydroxy-5-tert-octylphenyl-2H-benzotriazole UV- 5411 and 2-(2-hydroxy-3,5-di-tert-amylphenyl)-2H-benzotriazole UV-2337). United States Patent No. 5,964,905 teaches dyed and scented candle gels containing triblock copolymers and a hydrocarbon oil of high flash point. This reference teaches that a light (UV) absorber may be used to improve the shelf stability of the candle color when exposed to visible or ultraviolet light. Two preferred absorbers are ethylhexyl p- methoxycinnamate (PARSOL® MCX, Roche) and 2-(2-hydroxy-5-tert-octylphenyl)-2H- benzotriazole (CYASORB^® 5411 , Cytec).

One object of the invention is to provide for a white, dyed, dipped, unscented and/or scented candle wax stabilized by a UV absorber plus a hindered amine substituted on the N- atom by an alkoxy, a cycloalkoxy or a hydroxy-substituted alkoxy group.

The instant invention pertains to a composition which comprises

(a) white, dyed, dipped, unscented and/or scented candle wax, and

(b) an effective stabilizing amount of a combination of

(i) a UV absorber, and

(ii) a hindered amine substituted on the N-atom with an alkoxy, cycloalkoxy or a hydroxy-substituted alkoxy group or a mixture of said hindered amines,

wherein the ratio by weight of (i) to (ii) is from 10:1 to 1 :10; preferably 4:1 to 1 :4; most preferably 2:1 to 1 :2.

An effective amount of the UV absorber plus the hindered amine in the candle wax is 0.01 to 10% by weight, preferably 0.1 to 2% by weight; and most preferably 0.1 to 0.5% by weight based on the wax.

Preferably the UV absorber of component (i) is a benzotriazole, a benzophenone, an α-cyanoacrylate, an oxanilide, an s-triazine, a cinnamate, a malonate, a benzoate or a salicylate, or a mixture thereof. Most preferably the UV absorber of component (i) is a benzotriazole, a benzophenone or an s-triazine ; especially a benzotriazole.

The UV absorbers are well known in the field of stabilization of substrates from degradation caused by exposure to actinic radiation. Examples of UV absorbers which may be used beneficially in candles include the following:

(a) 4-octyloxy-2-hydroxybenzophenone;

(b) 4-methoxy-2-hydroxybenzophenone;

(c) 2-(2-hydroxy-5-methylphenyl)-2H-benzotriazole; (d) 2-(2-hydroxy-5-tert-octylphenyl-2H-benzotriazole;

(e) 2-(2-hydroxy-3,5-di-tert-amylphenyl)-2H-benzotriazole;

(f) octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate; (g) 2-(2-hydroxy-3,5-di-tert-butylphenyl)-2H-benzotriazole;

(h) 2-(2-hydroxy-5-tert-butylphenyl)-2H-benzotriazole;

(i) 5-chloro-2-(2-hydroxy-3,5-di-tert-butylphenyl)-2H-benzotriazole;

(j) 5-chloro-2-(2-hydroxy-3-tert-butyl-5-methylphenyl)-2H-benzotriazole;

(k) 2-(2-hydroxy-3-sec-butyl-5-tert-butylphenyl)-2H-benzotriazole;

(I) 2-(2-hydroxy-4-octyloxyphenyl)-2H-benzotriazole;

(m) 2-(2-hydroxy-3-dodecyl-5-methylphenyl)-2H-benzotriazole;

(n) 2-[2-hydroxy-3,5-di(α,α-dimethylbenzyl)phenyl]-2H-benzotriazole;

(o) 2-[2-hydroxy-3-(α,α-dimethylbenzyl)-5-tert-octylphenyl]-2H-benzotriazole;

(p) 2-{2-hydroxy-3-tert-butyl-5-[2-(omega-hydroxy-octa(ethyieneoxy)carbonyl)ethyl] phenyl}-2H-benzotriazole;

(q) 2-{2-hydroxy-3-tert-butyl-5-[2-(octyloxy)carbonyl)ethyl]phenyl}-2H- benzotriazole;

(r) 2-ethylhexyl p-methoxycinnamate;

(s) 4-methoxy-2,2'-dihydroxybenzophenone;

(t) 4,4'dimethoxy-2,2'-dihydroxybenzophenone;

(u) 2,4-bis(2,4-dimethylphenyl)-6-(2-hydroxy-4-octyloxyphenyl)-s-triazine;

(v) 2,4-diphenyl-6-(2-hydroxy-4-hexyloxyphenyl)-s-triazine;

(w) 2,4-bis(2,4-dimethylphenyl)-6-[2-hydroxy-4-(3-do-/tri-decyloxy-2-hydroxy propoxy)phenyl]-s-triazine; and

(x) 2,4-bis(2,4-dimethylphenyl)-6-[2-hydroxy-4-(3-do-/tri-decyloxy-2-hydroxypropoxy)-

5-α-cumylphenyl]-s-triazine. Preferably, the UV absorber is

(a) 4-octyloxy-2-hydroxybenzophenone;

(b) 4-methoxy-2-hydroxybenzophenone; (d) 2-(2-hydroxy-5-tert-octylphenyl-2H-benzotriazole;

(o) 2-[2-hydroxy-3-(α,α-dimethylbenzyl)-5-tert-octylphenyl]-2H-benzotriazole;

(p) 2-{2-hydroxy-3-tert-butyl-5-[2-(omega-hydroxy-octa(ethyleneoxy)carbonyl)ethyl] phenyl}-2H-benzotriazole; or

(q) 2-{2-hydroxy-3-tert-butyl-5-[2-(octyloxy)carbonyl)ethyl]phenyl}-2H- benzotriazole.

The hindered amines substituted on the N-atom by an alkoxy or a cycloalkoxy moiety are well known in the art. These are described in detail in United States Patent No. 5,204,473, the relevant parts of which are incorporated herein by reference.

The hindered amines substituted on the N-atom by an alkoxy, cycloalkoxy or benzyloxy moiety which are useful in the instant invention include the following:

(a) bis(1-octyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate;

(b) bis(1 -cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate;

(c) 1-cyclohexyloxy-2,2,6,6-tetramethyl-4-octadecylaminopiperidine;

(d) 2,4-bis[(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-6-(2- hydroxyethylamino-s-triazine;

(e) bis(1 -cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) adipate;

(f) the oligomeric compound which is the condensation product of 4,4'-hexamethylene bis(amino-2,2,6,6-tetramethylpiperidine) and 2,4-dichloro-6-[(1 -octyloxy-2,2,6,6-tetra- methylpiperidin-4-yl)butylamino]-s-triazine end-capped with 2-chloro-4,6-bis(dibutyl- amino)-s-triazine;

(g) the oligomeric compound which is the condensation product of 4,4'-hexamethylene- bis(amino-2,2,6,6-tetramethylpiperidine) and 2,4-dichloro-6-[(1 -cyclohexyloxy-2,2,6,6- tetramethylpiperidin-4-yl)butylamino]-s-triazine end-capped with 2-chloro-4,6- bis(dibutylamino)-s-triazine;

(h) 1 -methoxy-4-hydroxy-2,2,6,6-tetramethylpiperidine;

(i) 1 -octyloxy-4-hydroxy-2,2,6,6-tetramethylpiperidine;

0) 1 -cyclohexyloxy-4-hydroxy-2,2,6,6-tetramethylpiperidine; (k) 1 -methoxy-4-oxo-2,2,6,6-tetramethyipiperidine;

(I) 1 -octyloxy-4-oxo-2,2,6,6-tetramethylpiperidine;

(m) 1 -cyclohexyloxy-4-oxo-2,2,6,6-tetramethylpiperidine,

(n) bis(1-heptyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate,

(o) bis(1-nonyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate,

(p) bis(1-dodecyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate, or

(q) N,N',N",N"'-tetrakis[(4,6-bis(butyl-1-octyloxy-2,2,6,6-pentamethyipiperidin-4-yl)- amino-s-triazin-2-yl]-1 ,10-diamino-4,7-diazadecane.

The hindered amines substituted on the N-atom by a hydroxy-substituted alkoxy group are disclosed in GB 2347928 whose relevant parts are also incorporated herein by reference.

The hindered amines substituted on the N-atom by a hydroxy-substituted alkoxy moiety which are useful in the instant invention include the following:

(a) 1-(2-hydroxy-2-methylpropoxy)-4-octadecanoyloxy-2,2,6,6-tetramethylpiperidine;

(b) 1-(2-hydroxy-2-methylpropoxy)-4-hydroxy-2,2,6,6-tetramethylpiperidine;

(c) 1-(2-hydroxy-2-methylpropoxy)-4-oxo-2,2,6,6-tetramethylpiperidine;

(d) bis(1 -(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) sebacate;

(e) bis(1 -(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) adipate;

(f) bis(1 -(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) succinate;

(g) bis(1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) glutarate; and (h) 2,4-bis{N-[1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl]-N-butyl- amino}-6-(2-hydroxyethylamino)-s-triazine.

A most preferred composition is wherein component (i) is octyl 3-(benzotriazol-2-yl)-5-tert- butyl-4-hydroxyhydrocinnamate, and component (ii) is bis(1-octyloxy-2,2,6,6-tetramethyl- piperidin-4-yl) sebacate.

It is also contemplated that mixtures of the N-alkoxy or cyclohexyloxy substituted hindered amines; mixtures of the N-hydroxy-alkoxy substituted hindered amines; and mixtures of these two types of hindered amines can be used in the instant invention. Indeed, mixtures of these types of hindered amines along with conventional hindered amines where the N-atom is substituted by hydrogen, alkyl, acyl and the like are also contemplated as being useful in this invention.

Additionally, the stabilized candle wax composition may also include an antioxidant.

Preferred are antioxidants such as the phenolic antioxidants, phosphites or hydroxylamines.

The effective amount of the UV absorber in combination with the hindered amine and an antixoxidant in the candle wax is 0.01 to 10% by weight based on the wax; preferably is 0.1 to 2% by weight based on the wax; or most preferably is 0.1 to 0.5% by weight based on the wax.

Examples of such phenolic antioxidants and hydroxylamines include the following:

n-octadecyl 3,5-di-tert-butyl-4-hydroxyhydrocinnamate, neopentanetetrayl tetrakis(3,5-di-tert-butyl-4-hydroxyhydrocinammate), di-n-octadecyl 3,5-di-tert-butyl-4-hydroxybenzylphosphonate,

1 ,3,5-tris(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanurate, thiodiethylene bis(3,5-di-tert-butyl-4-hydroxyhydrocinnamate),

1,3,5-trimethyl-2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)benzene,

3,6-dioxaoctamethylene bis(3-methyl-5-tert-butyl-4-hydroxyhydrocinnamate),

2,6-di-tert-butyl-p-cresol,

2,2'-ethylidene-bis(4,6-di-tert-butylphenol),

1 ,3,5-tris(2,6-dimethyl-4-tert-butyl-3-hydroxybenzyl) isocynurate,

1 ,1 ,3,-tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane,

1 ,3,5-tris[2-(3,5-di-tert-butyl-4-hydroxyhydrocinnamoyloxy)ethyl] isocyanurate,

3,5-di-(3,5-di-tert-butyl-4-hydroxybenzyl)mesitol, hexamethylene bis(3,5-di-tert-butyl-4-hydroxyhydrocinnamate),

1-(3,5-di-tert-butyl-4-hydroxyanilino)-3,5-di(octylthio)-s-triazine,

N,N'-hexamethylene-bis(3,5-di-tert-butyl-4-hydroxyhydrocinnamamide), calcium bis(ethyl 3,5-di-tert-butyl-4-hydroxybenzylphosphonate), ethylene bis[3,3-di(3-tert-butyl-4-hydroxyphenyl)butyrate], octyl 3,5-di-tert-butyl-4-hydroxybenzylmercaptoacetate, bis(3,5-di-tert-butyl-4-hydroxyhydrocinnamoyl)hydrazide, N,N'-bis[2-(3,5-di-tert- butyl- 4-hydroxyhydrocinnamoyloxy)-ethyl]oxamide, and

N,N-dialkylhydroxylamine prepared from di(hydrogenated tallow)amine by direct oxidation.

A most preferred phenolic antioxidant is neopentanetetrayl tetrakis(3,5-di-tert-butyl-4-hydroxyhydrocinnamate), n-octadecyl 3,5-di-tert-butyl-4-hydroxyhydrocinnamate,

1 ,3,5-trimethyl-2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)benzene,

1 ,3,5-tris(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanurate,

2,6-di-tert-butyl-p-cresol, or

2,2'-ethylidene-bis(4,6-di-tert-butylphenol).

It should be noted that candles contain a host of various components. The base materials may be made up of the following:

paraffin wax, natural oils, polyamide plus fatty acid/ester, fatty acids such as stearin, opacifiers, beeswax, glycerides plus oxidized wax, alcohols, and ethyiene oligomers.

Candles also contain a number of additives such as the following:

mold release agents, fragrances, insect repellants or insecticides, hardeners, crystal modifiers, clarifiers, guttering reducers, colorants, f.p. control agents, stretchability improvers, gelling agents, extrusion aids, and vortex reducers.

Each of the various components are meant to control or modify the properties of the candle to insure proper burning, reduce channelling, aid in uniform melting, and the like. The colorants and fragrances obviously are there to provide the proper color, scent or other aesthetic appeal.

Candles may be scented or unscented; or they can be dyed or white (natural color of petroleum wax) or pigmented white; or they may be dipped into a solution of formulated wax to that a coating of said formulated wax is present only on the outside of the candle.

Of increasing importance are the transparent gel candles which look like clear glass, but which burn like a classical candle. As is discussed in detail in United States Patent No. 5,879,694, the relevant parts of which are incorporated herein by reference, these gel candles usually contain a copolymer selected from the group consisting of a triblock, radial block, diblock or multiblock copolymer classically made up of at least two thermodynamically incompatible segments containing both hard and soft segments. Typical of such block copolymers is KRATON® (Shell Chemical Co.) which consists of block segments of styrene monomer units and rubber monomer or comonomer units. The most common structure found in KRATON^® D series is a linear ABA block with styrene-butadiene-styrene (SBS) or styrene-isoprene-styrene (SIS).

Additionally, it is discovered that the use of a hindered amine substituted by an alkoxy moiety or by a hydroxy-substituted alkoxy moiety, as described above, even in the absence of a UV absorber provides to a candle made using candle wax stabilized therewith superior properties in terms of the prevention of the undesired channelling during the burning of the candle. This control or modification of burning properties of the candle leads to uniform burning in a controlled way and the prevention of undesired cavitation in the candle caused by uncontrolled and uneven burning.

The following examples are meant for illustrative purposes only and are not to be construed to limit the instant invention in any manner whatsoever.

Raw Materials

Fully refined wax with a melting point of 137-141 °C and <0.5% oil content is obtained from the Astor Wax Company.

Dyes are supplied by French Color and Chemical Corporation.

Additional wax samples are supplied by the Candle Lite Corporation of America. These samples contained red, green or yellow dyes and fragrances.

The UV absorbers and hindered amine stabilizers are obtained from the Ciba Speciality Chemicals Corporation.

Sample Preparation

The wax samples obtained from the Candle Lite Corporation of America already contain a dye and a fragrance (scent). In these cases, the wax is melted and the appropriate stabilizer(s) is (are) added and dissolved in the molten wax. The stabilized wax is then poured into a mold (7" x 8.5" x 0.25"; 17.78 cm x 21.59 cm x 0.635 cm) giving a wax plaque.

To the wax samples obtained from the Astor Wax Company after melting are added 0.001 % by weight of the test dyes to give a dyed candle wax base. To the dyed wax base after melting is (are) added the appropriate stabilizer(s). The melted stabilized and dyed wax is then poured into the mold described above to give a wax plaque. Sa ple Exposure

The wax plaques described above are cut into eight equal pieces (3.5" x 2.125"; 8.89 cm x 5.40 cm). Triplicate samples of each are exposed under a bank of six (6) cool-white fluorescent lamps (40 watts) or under a bank of six (6) UV lamps having a wavelength of 368 nm with the test samples being twelve (12) inches (30.48 cm) below the lamps.

Dye color fade (or color change) is measured by a Macbeth ColorEye Spectrophotometer with a 6 inch integrating sphere. The conditions are: 10 degree observer; D65 illuminant and 8 degree viewing angle.

Initial color measurements are taken using the above parameters. The L, a and b values are calculated using the CIE system from the reflectance values. Yl is calculated from the L, a and b values. Subsequent measurements are taken at specified intervals. Delta L, a, b and Yl values are simply the difference between the initial values and the values at each interval. Delta(Δ) E is calculated as follows:

[(Delta L)² + (Delta a)² + (Delta b)²]^1/2 = Delta E.

Example 1

Color Fade of Red #C-15 in Unscented Candle Wax under Fluorescent Lamp Exposure

A variety of different stabilizers are evaluated in unscented candle wax which contains Red #C-15 under fluorescent lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired. ΔE after Sample^* (wt% add) 3 days 6 days 9 days

Blank (no add) 2.35 5.58 8.69

A (0.2%) 2.32 2.72 3.35

B (0.2%) 1.13 2.02 2.90

C (0.2%) 1.92 4.31 7.16

A (0.1%) +

B (0.1%) 0.27 0.55 0.75

A (0.1%) +

C (0.1%) 0.35 0.32 0.62

^*A is octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate, TINUVIN® 384, CIBA.

B is bis(1 ,2,2,6,6-pentamethylpiperdin-4-yl) sebacate, TINUVIN® 292, CIBA).

C is bis(1-octyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate, TINUVIN® 123, CIBA).

These data show that Compound C, a hindered amine substituted on the N-atom by an alkoxy moiety, does not stabilize candle wax when used alone as well as a conventional hindered amine Compound B, but when used in combination with a benzotriazole UV absorber provides far superior stabilization efficacy.

Example 2

Color Fade of Red #C-15 in Unscented Candle Wax under UV Lamp Exposure A variety of different stabilizers are evaluated in unscented candle wax which contains Red #C-15 under UV lamp exposure at 368 nm wavelength. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample^* (wt% add) 3 days 11 days 42 days

Blank (no add) 12.99 32.85 33.42

A (0.2%) 1.31 4.93 14.49

C (0.2%) 9.52 23.85 32.51

A (0.1%) +

C (0.1%) 1.12 3.12 7.48

^*A is octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate, TINUVIN® 384, CIBA. C is bis(1-octyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate, TINUVIN® 123, CIBA).

These data show that Compound C, a hindered amine substituted on the N-atom by an alkoxy moiety, does not stabilize red candle wax when used alone as well as a conventional benzotriazole Compound A, but when used in combination with a benzotriazole UV absorber provides far superior stabilization efficacy than when either stabilizer are used alone.

Example 3

Color Fade of Yellow #C-47 in Unscented Candle Wax under Fluorescent Lamp Exposure

A variety of different stabilizers are evaluated in unscented candle wax which contains Yellow #C-47 under fluorescent lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample* (wt% add) 9 days 21 days 40 days

A (0.2%) 0.60 0.76 3.32

D (0.2%) 0.46 0.71 1.41

D (0.1%) +

E (0.1 %) 0.40 0.76 1.85

C (0.2%) 0.74 0.71 1.20

A (0.1%) +

C (0.1%) 0.43 0.47 0.87

^*A is octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate, TINUVIN® 384, CIBA. C is bis(1-octyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate, TINUVIN® 123, CIBA). D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA. E is 4-octyloxy-2-hydroxybenzophenone, CHIMASSORB® 81 , CIBA.

The combination of a conventional benzotriazole Compound A with a hindered amine substituted on the N-atom by an alkoxy moiety provides far superior protection for the yellow dyed unscented candle than like stabilizers used alone.

Example 4

Color Fade of Yellow #C-47 in Unscented Candle Wax under UV Lamp Exposure A variety of different stabilizers are evaluated in unscented candle wax which contains Yellow #C-47 under UV lamp exposure at 368 nm wavelength. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample^* (wt% add) 41 days 80 days 121 days

Blank (no add) 7.25 12.85 15.16

A (0.2%) 5.25 9.35 11.06

C (0,2%) 2.62 5.48 6.64

A (0.1%) +

B (0.1%) 0.94 2.60 3.30

A (0.1%) +

C (0.1%) 1.31 2.18 2.53

B is bis(1 ,2,2,6,6-pentamethylpiperdin-4-yl) sebacate, TINUVIN® 292, CIBA).

These data show that Compound C, a hindered amine substituted on the N-atom by an alkoxy group in combination with a conventional benzotriazole UV absorber, clearly protect the yellow dye in the unscented candle wax far better than conventional UV absorber in combination with a conventional hindered amine Compound B. Example 5

Color Fade of Blue #C-19 in Unscented Candle Wax under Fluorescent Lamp Exposure

A variety of different stabilizers are evaluated in unscented candle wax which contains Blue #C-19 under fluorescent lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample^* (wt% add) 6 days 28 days 54 days

Blank (none) 9.74 42.51 44.00

A (0.2%) 0.37 3.57 11.29

D (0.2%) 0.47 2.69 8.14

C (0.2%) 5.60 11.05 14.55

D (0.1%) +

E (0.1%) 0.47 2.57 7.71

A (0.1%) +

C (0.1%) 0.32 2.23 4.12

^*A is octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate, TINUVIN® 384, CIBA. C is bis(1-octyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate, TINUVIN® 123, CIBA). D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA. E is 4-octyloxy-2-hydroxybenzophenone, CHIMASSORB® 81 , CIBA. The combination of a conventional benzotriazole Compound A with a hindered amine substituted on the N-atom by an alkoxy moiety provides far superior protection for the blue dyed unscented candle than like stabilizers used alone.

Example 6

Color Fade of Blue #C-19 in Unscented Candle Wax under UV Lamp Exposure

A variety of different stabilizers are evaluated in unscented candle wax which contains Blue #C-19 under UV lamp exposure at 368 nm wavelength. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample* (wt% add) 2 days 24 days 42 days

Blank (no add) 12.54 26.87 26.86

A (0.2%) 0.51 4.07 8.75

D (0.2%) 0.41 3.12 6.64

C (0.2%) 6.39 12.92 15.49

D (0.1%) +

E (0.1%) 0.72 3.64 7.55

A (0.1%) +

C (0.1%) 0.73 2.96 4.27

^*A is octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate, TINUVIN® 384, CIBA. C is bis(1 -octyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate, TINUVIN® 123, CIBA). D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA. E is 4-octyloxy-2-hydroxybenzophenone, CHIMASSORB® 81 , CIBA.

The combination of a conventional benzotriazole Compound A with a hindered amine substituted on the N-atom by an alkoxy moiety provides far superior protection for the blue dyed unscented candle than like stabilizers used alone.

Example 7

Color Change of a White Unscented Candle Wax under Fluorescent Lamp Exposure

The combination of 0.2% by weight of octyl 3-(p-methoxyphenyl)-3-phenyl-α-cyano- acrylate and 0.2% by weight of the oligomeric compound which is the condensation product of 4,4'-hexamethylenebis(amino-2,2,6,6-tetramethylpiperidine) and 2,4-dichloro-6-[(1-cyclo- hexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-s-triazine end-capped with 2-chloro- 4,6-bis(dibutylamino)-s-triazine protect the white unscented candle wax well from discoloration.

Example 8

Color Change of White Unscented Candle Wax under UV Lamp Exposure

The combination of 0.2% by weight of pentaerythrityl tetrakis[3,3-diphenyl-α-cyano- acrylate] and 0.2% by weight of 1-methoxy-4-hydroxy-2,2,6,6-tetramethylpiperidine protect the white unscented candle wax well from discoloration. Example 9

Color Change of Yellow Scented Candle Wax under Fluorescent Lamp Exposure

A variety of different stabilizers are evaluated in yellow scented candle wax obtained from the Candle Lite Corporation of America under fluorescent lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample^* (wt% add) 9 days 20 days 26 days

Blank (no add) 6.15 9.41 9.27

A (0.2%) 5.07 8.02 8.54

D (0.2%) 5.28 8.29 9.20

E (0.2%) 4.62 7.67 8.83

A (0.1%) +

C (0.1 %) 4.43 7.37 8.20

These data show that a combination of a conventional benzotriazole UV absorber with a hindered amine having the N-atom substituted by an alkoxy moiety provides superior resistance to discoloration than the benzotriazole alone. Example 10

Color Change of Yellow Scented Candle Wax under UV Lamp Exposure

A variety of different stabilizers are evaluated in yellow scented candle wax obtained from the Candle Lite Corporation of America under UV lamp exposure at 368 nm wavelength. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample^* (wt% add) 7 days 1 1 days 15 days

Blank (no add) 4.88 4.97 5.06

A (0.2%) 3.16 3.54 4.33

D (0.2%) 3.56 4.06 5.05

E (0.2%) 4.57 5.41 5.92

D (0.1%) +

E (0.1%) 3.96 4.50 5.35

A (0.1%) +

C (0.1%) 2.69 3.23 3.72

^*A is octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate, TINUVIN® 384, CIBA. C is bis(1 -octyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate, TINUVIN® 123, CIBA). D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA. E is 4-octyloxy-2-hydroxybenzophenone, CHIMASSORB® 81 , CIBA. These data show that a combination of a conventional benzotriazole UV absorber with a hindered amine having the N-atom substituted by an alkoxy moiety provides superior resistance to discoloration than using a benzotriazole alone.

Example 11

Color Fade of Red Scented Candle Wax under UV Lamp Exposure

A variety of different stabilizers are evaluated in red scented candle wax obtained from the Candle Lite Corporation of America under UV lamp exposure at 368 nm wavelength. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample^* (wt% add) 16 days 35 days 54 days

Blank (no add) 21.54 50.82 52.51

A (0.2%) 5.85 7.05 7.77

D (0.2%) 5.59 6.92 7.67

E (0.2%) 6.58 11.15 12.58

D (0.1%) +

E (0.1%) 5.25 6.47 7.32

A (0.1%) +

C (0.1%) 4.56 5.22 5.46

These data show that a combination of a conventional benzotriazole UV absorber with a hindered amine having the N-atom substituted by an alkoxy moiety provides superior resistance to discoloration than using a benzotriazole alone.

Example 12

Color Fade of Green Scented Candle Wax under Fluorescent Lamp Exposure A variety of different stabilizers are evaluated in green scented candle wax obtained from the Candle Lite Corporation of America under flourescent lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample^* (wt% add) 9 days 14 days 26 days

Blank (no add) 5.05 4.88 10.94

A (0.2%) 2.92 2.66 7.13

D (0.2%) 3.23 2.64 7.42

E (0.2%) 2.82 2.55 7.76

D (0.1%) +

E (0.1 %) 2.46 1.94 6.15

A (0.1%) +

B (0.1%) 2.84 1.43 2.15

A (0.1 %) +

C (0.1%) 2.42 0.95 1.93 ^*A is octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate, TINUVIN® 384, CIBA.

B is bis(1 ,2,2,6,6-pentamethylpiperdin-4-yl) sebacate, TINUVIN® 292, CIBA).

D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA.

E is 4-octyloxy-2-hydroxybenzophenone, CHIMASSORB® 81 , CIBA.

These data show that a combination of a conventional benzotriazole UV absorber with a hindered amine provides far better stabilization efficacy than a benzotriazole alone at the same total concentration; and especially when the hindered amine is substituted on the N- atom by an alkoxy moiety.

Example 13

Color Fade of Green Scented Candle Wax under UV Lamp Exposure

A variety of different stabilizers are evaluated in green scented candle wax obtained from the Candle Lite Corporation of America under UV lamp exposure at 368 nm wavelength. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample^* (wt% add) 7 days 17 days 25 days

Blank (no add) 6.35 8.89 9.93

A (0.2%) 0.26 1.34 1.94

D (0.2%) 0.73 2.11 2.86

E (0.2%) 4.17 7.39 8.73 D (0.1%) +

E (0.1%) 1.64 3.45 4.48

A (0.1%) +

C (0.1%) 0.36 0.78 1.22

These data show that conventional benzotriazole UV absorbers are far superior to benzophenone UV absorbers in protecting the green scented candle wax from discoloration, but that a combination of a conventional benzotriazole UV absorber with a hindered amine substituted on the N-atom by an alkoxy moiety provides far superior stabilization from discoloration.

Example 14

Color Fade of Blue Scented Candle Wax under Fluorescent Lamp Exposure

A variety of different stabilizers are evaluated in blue scented candle wax obtained from the Candle Lite Corporation of America under fluorescent lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired. ΔE after Sample^* (wt% add) 9 days 14 days 26 days

Blank (no add) 6.61 7.90 12.03

A (0.2%) 5.40 6.23 8.50

D (0.2%) 4.69 5.61 7.90

E (0.2%) 4.76 4.93 7.60

D (0.1%) +

E (0.1%) 4.60 5.14 7.62

A (0.1 %) +

C (0.1 %) 4.23 4.95 6.44

^*A is octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate, TINUVIN® 384, CIBA. C is bis(1-octyloxy-2,2,6,6-tetramethyipiperidin-4-yl) sebacate, TINUVIN® 123, CIBA). D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA. E is 4-octyloxy-2-hydroxybenzophenone, CHIMASSORB® 81 , CIBA.

These data show that a combination of a conventional benzotriazole UV absorber with a hindered amine substituted on the N-atom by an alkoxy moiety provides far superior stabilization from discoloration for the blue scented candle wax than a UV absorber alone.

Example 15

Color Fade of Blue Scented Candle Wax under UV Lamp Exposure

A variety of different stabilizers are evaluated in blue scented candle wax obtained from the Candle Corporation of America under UV lamp exposure at 368 nm wavelength. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample* (wt% add) 16 days 36 days 54 days

Blank (no add) 32.88 40.61 43.82

A (0.2%) 8.86 13.58 16.05

D (0.2%) 8.30 14.76 18.75

E (0.2%) 15.20 19.49 22.94

D (0.1%) +

E (0.1%) 9.42 15.80 19.53

A (0.1%) +

B (0.1%) 5.59 8.42 9.57

A (0.1%) +

C (0.1%) 5.89 7.19 8.03

B is bis(1 ,2,2,6,6-pentamethylpiperdin-4-yl) sebacate, TINUVIN® 292, CIBA).

C is bis(1 -octyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate, TINUVIN® 123, CIBA).

D is 2-(2-hydroxy-5-tert-octyIphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA.

E is 4-octyloxy-2-hydroxybenzophenone, CHIMASSORB® 81 , CIBA.

These data show that a combination of a conventional UV absorber with a hindered amine provides a significantly better protection for the blue scented candle wax than a UV absorber alone. When the hindered amine is also substituted on the N-atom by an alkoxy moiety even much better stabilization efficacy is achieved. Example 16

Green scented candle wax as described in Example 12 is well stabilized by 0.2% by weight of dimethyl p-methoxybenzylidenemalonate, SANDUVOR® PR 25, in combination with 0.2% by weight of bis(1-octyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate, TINUVIN® 123, CIBA.

Example 17

Yellow scented candle wax as described in Example 10 is well stabilized by 0.1 % by weight of di(1 , 2,2,6, 6-pentamethylpiperidin-4-yl) p-methoxybenzylidenemalonate, SANDUVOR® PR 31 , in combination with 0.1 % by weight of 1-(2-hydroxy-2-methylpropoxy)- 4-octadecanoyloxy-2,2,6,6-tetramethylpiperidine.

Example 18

Red unscented candle wax as described in Example 1 is well stabilized by 0.1 % by weight of dimethyl di(p-chlorophenyl)methylenemalonate in combination with 0.1% by weight of bis(1 -(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) glutarate.

Example 19

Red unscented candle wax as described in Example 2 is well stabilized by 0.2% by weight of dimethyl di(p-methoxyphenyl)methylenemalonate in combination with 0.2% by weight of bis(1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) succinate.

Example 20 Red unscented candle wax as described in Example 1 is well stabilized by 0.1% by weight of 4,4'-dimethoxy-2,2'-dihydroxybenzophenone in combination with 0.1 % by weight of bis(1-octyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate, TINUVIN® 123, CIBA).

Example 21

Red unscented candle wax as described in Example 2 is well stabilized by 0.2% by weight of 4-tert-butylphenyl 2-hydroxybenzoate in combination with 0.1 % by weight of 2,4- bis[(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-6-(2-hydroxyethylamino-s- triazine.

Example 22

Yellow unscented candle wax as described in Example 3 is well stabilized by 0.2% by weight of 2-ethoxy-2-ethyloxanilide in combination with 0.1% by weight of bis(1-cyclohexyl- oxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate.

Example 23

Yellow unscented candle wax as described in Example 4 is well stabilized by 0.2% by weight of 3-hydroxyphenyl benzoate in combination with 0.2% by weight of 1 -cyclohexyloxy- 2,2,6,6-tetramethyl-4-octadecylaminopiperidine.

Example 24

Blue unscented candle wax as described in Example 5 is well stabilized by 0.2% by weight of dodecyl 3-phenyl-3-methyl-α-cyanoacrylate in combination with 0.1% by weight of bis(1-cyclohexyioxy-2,2,6,6-tetramethylpiperidin-4-yl) adipate. Example 25

Blue unscented candle wax as described in Example 6 is well stabilized by 0.2% by weight of dodecyl 3,3-diphenyl-α-cyanoacrylate in combination with 0.2% by weight of the oligomeric compound which is the condensation product of 4,4'-hexamethylenebis(amino- 2,2,6,6-tetramethylpiperidine) and 2,4-dichloro-6-[(1 -octyloxy-2,2,6,6-tetramethylpiperidin-4- yl)butylamino]-s-triazine end-capped with 2-chloro-4,6-bis(dibutylamino)-s-triazine.

Example 26

Yellow scented candle wax as described in Example 9 is well stabilized by 0.2% by weight of 2-{2-hydroxy-3-tert-butyl-5-[2-(omega-hydroxy-octa(ethyleneoxy)carbonyl)ethyl]- phenyl}-2H-benzotriazole, TINUVIN® 1130, CIBA, in combination with 1 -octyloxy-4-hydroxy- 2,2,6,6-tetramethylpiperidine.

Example 27

Yellow scented candle wax as described in Example 10 is well stabilized by 0.1 % by weight of 2-[2-hydroxy-3-(α, -dimethylbenzyl)-5-tert-octylphenyl]-2H-benzotriazole, TINUVIN® 928, CIBA, in combination with 0.2% by weight of 1-cyclohexyloxy-4-hydroxy- 2,2,6,6-tetramethylpiperidine.

Example 28

Red scented candle wax as described in Example 11 is well stabilized by 0.1% by weight of 5-chloro-2-(2-hydroxy-3-tert-butyl-5-methylphenyl)-2H-benzotriazole, TINUVIN® 326, CIBA, in combination with 0.1 % by weight of 1-cyclohexyloxy-4-oxo-2,2,6,6-tetramethyl- piperidine. Example 29

Green scented candle wax as described in Example 12 is well stabilized by 0.1% by weight of octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate, TINUVIN® 384, CIBA, in combination with 0.1% by weight of 1-octyloxy-4-oxo-2,2,6,6-tetramethylpiperidine.

Example 30

Green scented candle wax as described in Example 13 is well stabilized by 0.1% by weight of octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate, TINUVIN® 384, CIBA, in combination with 0.1% by weight of 1 -(2-hydroxy-2-methylpropoxy)-4-octadecanoyl- oxy-2,2,6,6-tetramethylpiperidine.

Example 31

Blue scented candle wax as described in Example 14 is well stabilized by 0.1% by weight of 2-(2-hydroxy-5-tert-octylphenyl-2H-benzotriazole, TINUVIN® 329, in combination with 0.1% by weight of 1-(2-hydroxy-2-methylpropoxy)-4-hydroxy-2,2,6,6-tetramethyl- piperidine.

Example 32

Blue scented candle wax as described in Example 15 is well stabilized by 0.2% by weight of 4-octyloxy-2-hydroxybenzophenone in combination with 0.1 % by weight of 1-(2- hydroxy-2-methylpropoxy)-4-oxo-2,2,6,6-tetramethylpiperidine. Example 33

Red unscented candle wax as described in Example 1 is well stabilized by 0.2% by weight of 2-ethylhexyl p-methoxycinnamate in combination with 0.1 % by weight of bis(1-(2- hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) sebacate.

Example 34

Red unscented candle wax as described in Example 2 is well stabilized by 0.1 % by weight of 4,4'-dimethoxy-2,2'dihydroxybenzophenone in combination with 0.1 % by weight of bis(1 -(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) adipate.

Example 35

Yellow unscented candle wax as described in Example 3 is well stabilized by 0.1% by weight of 2-ethoxy-2'-ethyl-5,4'-di-tert-butyloxanilide in combination with 0.1 % by weight of bis(1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) succinate.

Example 36

Yellow unscented candle wax as described in Example 4 is well stabilized by 0.1% by weight of 2,4-bis(2,4-dimethylphenyl)-6-[2-hydroxy-4-(3-do-/tri-decyloxy-2-hydroxypropoxy)- phenyl]-s-triazine, TINUVIN® 400, CIBA, in combination with 0.1% by weight of bis(1- octyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate, TINUVIN® 123, CIBA).

Example 37

Blue scented candle wax as described in Example 14 is well stabilized by 0.1% by weight of 2,4-bis(2,4-dimethylphenyl)-6-[2-hydroxy-4-(3-do-/tri-decyloxy-2-hydroxypropoxy)- 5-α-cumylphenyl]-s-triazine in combination with 0.1 % by weight of 2,4-bis[(1-cyclohexyloxy- 2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-6-(2-hydroxyethylamino-s-triazine.

Example 38

Blue unscented candle wax as described in Example 5 is well stabilized by 0.2% by weight of 2,4-bis(2,4-dimethylphenyl)-6-(2-hydroxy-4-octyloxyphenyl)-s-triazine in combination with 0.1 % by weight of 1-(2-hydroxy-2-methylpropoxy)-4-octadecanoyloxy- 2,2,6,6-tetramethylpiperidine.

Example 39

Blue unscented candle wax as described in Example 6 is well stabilized by 0.1 % by weight of 2,4-bis(2,4-dimethylphenyl)-6-[2-hydroxy-4-(3-do-/tri-decyloxy-2-hydroxypropoxy)- phenyl]-s-triazine, TINUVIN® 400, CIBA, in combination with 0.1% by weight of bis(1-(2- hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) sebacate.

Example 40

White unscented candle wax as described in Example 7 is well stabilized by 0.1% by weight of 4-tert-octylphenyl 2-hydroxybenzoate in combination with bis(1 -(2-hydroxy-2- methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) adipate.

Example 41

White unscented candle wax as described in Example 8 is well stabilized by 0.1% by weight of 3-hydroxyphenyl benzoate in combination with 0.1% by weight of bis(1-(2-hydroxy- 2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) succinate. Example 42

Yellow scented candle wax as described in Example 9 is well stabilized by 0.1 % by weight of dodecyl 3,3-diphenyl-α-cyanoacrylate in combination with 0.1% by weight of bis(1- (2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) glutarate.

Example 43

Yellow scented candle wax as described in Example 10 is well stabilized by 0.1% by weight of pentaerythrityl tetrakis[3,3-diphenyl-α-cyanoacrylate] in combination with 0.2% by weight of 2,4-bis{N-[1 -(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl]-N-butyl- amino}-6-(2-hydroxyethylamino)-s-triazine.

Example 44

Red scented candle wax as described in Example 11 is well stabilized by 0.2% by weight of octyl 3-(p-methoxyphenyl)-3-phenyl-α-cyanoacrylate in combination with 0.2% by weight of 1 -(2-hydroxy-2-methylpropoxy)-4-octadecanoyloxy-2,2,6,6-tetramethylpiperidine.

Example 45

Color Fade of Pink Scented Candle Wax under Fluorescent Lamp Exposure

A variety of different stabilizers are evaluated in pink scented candle wax obtained from the Candle-Lite Corporation under fluorescent lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired. ΔE after Sample^* (wt% add) 30 days

Blank (no add) 14.47

A (0.3%) 10.47

D (0.15%) +

E (0.15%) 8.93

A (0.15%) +

C (0.15%) 5.72

C (0.3%) 14.05

F (0.15%) +

G (0.15%) 3.90

D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA.

E is 4-octyloxy-2-hydroxybenzophenone, CHIMMASORB® 81 , CIBA.

F is 1 -(2-hydroxy-2-methylpropoxy)-4-octadecanoyloxy-2,2,6,6-tetramethylpiperidine.

G is 4,4'-dimethoxy-2,2'-dihydroxybenzophenone.

These data show that a hindered amine substituted on the N-atom with a alkoxy moiety (Compound C) or by a hydroxy-substituted alkoxy moiety (Compound F) in combination with a UV absorber protects the pink scented candle wax far better than conventional UV absorbers. Example 46

Color Fade of Pink Scented Candle Wax under UV Lamp Exposure

A variety of different stabilizers are evaluated in pink scented candle wax obtained from the Candle-Lite Corporation under UV lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample^* (wt% add) 32 days

Blank (no add) 21.10

D (0.15%) +

E (0.15%) 11.15

A (0.15%) +

B (0.15%) 9.84

B (0.3%) 16.24

F (0.15%) +

G (0.15%) 6.19

F (0.15%) +

A (0.15%) 7.84

B is bis(1 ,2,2,6,6-pentamethylpiperidin-4-yl) sebacate, TINUVIN® 292, CIBA.

D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA.

E is 4-octyloxy-2-hydroxybenzophenone, CHIMMASORB® 81 , CIBA.

G is 4,4'-dimethoxy-2,2'-dihydroxybenzophenone. These data show that a hindered amine substituted on the N-atom with a hydroxy- substituted alkoxy moiety (Compound F) in combination with a UV absorber protects the pink scented candle wax far better than conventional UV absorbers.

Example 47

Color Fade of White Scented Candle Wax under Fluorescent Lamp Exposure

A variety of different stabilizers are evaluated in white scented candle wax obtained from the Candle-Lite Corporation under fluorescent lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample^* (wt% add) 28 days

Blank (no add) 34.05

B (0.3%) 31.20

A (0.15%) +

B (0.15%) 29.49

B (0.15%) +

D (0.15%) 24.23

D (0.15%) +

E (0.15%) 20.10

F (0.15%) +

H (0.15%) 16.05 F (0.15%) +

I (0.15%) 15.04

F (0.15%) +

E (0.15%) 12.19

F (0.15%) +

A (0.15%) 10.48

*A is octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate, TINUVIN® 384, CIBA.

B is bis(1 ,2,2,6,6-pentamethylpiperidin-4-yl) sebacate, TINUVIN® 292, CIBA.

D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA.

E is 4-octyloxy-2-hydroxybenzophenone, CHIMMASORB® 81 , CIBA.

H is 2,4-bis(2,4-dimethylphenyl)-6-[2-hydroxy-4-(3-do-/tri-decyloxy-2-hydroxypropoxy)- phenyl]-s-triazine, TINUVIN® 400, CIBA.

I is 2,4-bis(2,4-dimethylphenyl)-6-[2-hydroxy-4-(3-do-/tri-decyloxy-2-hydroxypropoxy)-5-α- cumylphenyl]-s-triazine.

These data show that a hindered amine substituted on the N-atom with a hydroxy- substituted alkoxy moiety (Compound F) in combination with a UV absorber protects the pink scented candle wax far better than conventional UV absorbers.

Example 48

Color Fade of White Scented Candle Wax under UV Lamp Exposure

A variety of different stabilizers are evaluated in white scented candle wax obtained from the Candle-Lite Corporation under UV lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired. ΔE after Sample^* (wt% add) 25 days Blank (no add) 45.09

B (0.3%) 32.03

A (0.3%) 25.50

A (0.15%) +

B (0.15%) 29.74

D (0.15%) +

E (0.15%) 30.11

F (0.15%) +

A (0.15%) 13.97

B is bis(1 ,2,2,6,6-pentamethylpiperidin-4-yl) sebacate, TINUVIN® 292, CIBA.

D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA.

E is 4-octyloxy-2-hydroxybenzophenone, CHIMMASORB® 81 , CIBA.

The next four examples show the use of s-triazine UV absorbers with a hindered amine substituted on the N-atom with an alkoxy or hydroxy-substituted alkoxy moiety. Example 49

Color Fade of Pink Scented Candle Wax under UV Lamp Exposure

ΔE after Sample^* (wt% add) 32 days

Blank (no add) 21.10

B (0.3%) 16.24

D (0.15%) +

E (0.15%) 11.15

A (0.15%) +

B (0.15%) 9.84

J (0.15%) +

C (0.15%) 7.50

B is bis(1 ,2,2,6,6-pentamethylpiperidin-4-yl) sebacate, TINUVIN® 292, CIBA.

D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA.

E is 4-octyloxy-2-hydroxybenzophenone, CHIMMASORB® 81 , CIBA.

J is the compound prepared by the reaction of 2,4,6-tris(2,4-dihydroxyphenyl)-s-triazine and isooctyl α-bromopropionate in the presence of a base. These data show that a hindered amine substituted on the N-atom with a alkoxy moiety (Compound C) in combination with an s-triazine UV absorber protects the pink scented candle wax far better than conventional UV absorbers.

Example 50

Color Fade of Gray Scented Candle Wax under UV Lamp Exposure

A variety of different stabilizers are evaluated in gray scented candle wax obtained from the Candle-Lite Corporation under UV lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample^* (wt% add) 23 days

Blank (no add) 30.07

C (0.3%) 25.70

D (0.15%) +

E (0.15%) 10.96

A (0.3%) 9.14

A (0.15%) +

C (0.15%) 5.11

J (0.15%) +

C (0.15%) 4.57

D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA.

E is 4-octyloxy-2-hydroxybenzophenone, CHIMMASORB® 81 , CIBA.

J is the compound prepared by the reaction of 2,4,6-tris(2,4-dihydroxyphenyl)-s-triazine and isooctyl α-bromopropionate in the presence of a base.

These data show that a hindered amine substituted on the N-atom with an alkoxy moiety (Compound C) in combination with an s-triazine UV absorber protects the gray scented candle wax far better than conventional UV absorbers.

Example 51

Color Fade of White Scented Candle Wax under Fluorescent Lamp Exposure

ΔE after Sample^* (wt% add) 28 days

Blank (no add) 34.05

B (0.3%) 31.20

A (0.3%) 30.28

A (0.15%) +

B (0.15%) 29.49

B (0.15%) + D (0.15%) 24.23

D (0.15%) +

E (0.15%) 20.10

J (0.15%) +

C (0.15%) 13.80

B is bis(1 ,2,2,6,6-pentamethylpiperidin-4-yl) sebacate, TINUVIN® 292, CIBA.

D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA.

E is 4-octyloxy-2-hydroxybenzophenone, CHIMMASORB® 81 , CIBA.

These data show that a hindered amine substituted on the N-atom with an alkoxy moiety (Compound C) in combination with an s-triazine UV absorber protects the white scented candle wax far better than conventional UV absorbers.

Example 52

Color Fade of White Scented Candle Wax under UV Lamp Exposure

A variety of different stabilizers are evaluated in white scented candle wax obtained from the Candle-Lite Corporation under UV lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired. ΔE after

Sample^* (wt% add) 25 davs

Blank (no add) 45.09

C (0.3%) 36.32

B (0.3%) 32.03

A (0.3%) 25.50

A (0.15%) +

B (0.15%) 29.74

D (0.15%) +

E (0.15%) 30.11

J (0.15%) +

C (0.15%) 13.30

B is bis(1 ,2,2,6,6-pentamethylpiperidin-4-yl) sebacate, TINUVIN® 292, CIBA.

C is bis(1-octyloxy-2,2,6,6-tetramethyipiperidin-4-yl) sebacate, TINUVIN® 123, CIBA).

D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA.

E is 4-octyloxy-2-hydroxybenzophenone, CHIMMASORB® 81 , CIBA.

J is the compound prepared by the reaction of 2,4,6-tris(2,4-dihydroxyphenyl)-s-triazine and isooctyl -bromopropionate in the presence of a base.

These data show that a hindered amine substituted on the N-atom with an alkoxy moiety (Compound C) in combination with an s-triazine UV absorber protects the white scented candle wax far better than conventional UV absorbers. The next six examples show the use of various UV absorbers with a block oligomeric or other hindered amine substituted on the N-atom with an alkoxy or cycloalkoxy moiety.

Example 53

Color Fade of Pink Scented Candle Wax under Fluorescent Lamp Exposure

A variety of different stabilizers are evaluated in pink scented candle wax obtained from the Candle-Lite Corporation under fluorescent lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after Sample^* (wt% add) 30 davs

Blank (no add) 14.47

B (0.3%) 10.00

D (0.15%) +

E (0.15%) 8.93

B (0.15%) +

D (0.15%) 3.42

K (0.15%) +

L (0.15%) 2.14

M (0.15%) +

E (0.15%) 1.39

^*B is bis(1 ,2,2,6,6-pentamethylpiperidin-4-yl) sebacate, TINUVIN® 292, CIBA. D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA.

E is 4-octyloxy-2-hydroxybenzophenone, CHIMMASORB® 81 , CIBA.

K is a hindered amine prepared according to Example 1 of WO 98/54175.

L is 2,4-bis(biphenyl-4-yl)-6-(2-hydroxy-4-octyloxyphenyl)-s-triazine.

M is the compound prepared according to Example 4 of U.S. Patent No. 5,844,026.

These data show that a hindered amine substituted on the N-atom with a cycloalkoxy moiety (Compound K or M) in combination with a UV absorber protects the pink scented candle wax far better than conventional UV absorbers.

Example 54

Color Fade of Pink Scented Candle Wax under UV Lamp Exposure

ΔE after Sample^* (wt% add) 32 davs

Blank (no add) 21.10

B (0.3%) 16.24

D (0.15%) +

E (0.15%) 11.15

A (0.15%) +

B (0.15%) 9.84 N (0.15%) +

1 (0.15%) 7.10

M (0.15%) +

E (0.15%) 6.76

P (0.15%) +

O (0.15%) 4.85

K (0.15%) +

L (0.15%) 3.93

*B is bis(1 ,2,2,6,6-pentamethylpiperidin-4-yl) sebacate, TINUVIN® 292, CIBA.

D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA.

E is 4-octyloxy-2-hydroxybenzophenone, CHIMMASORB® 81 , CIBA.

K is a hindered amine prepared according to Example 1 of WO 98/54175.

L is 2,4-bis(biphenyl-4-yl)-6-(2-hydroxy-4-octyloxyphenyl)-s-triazine.

M is the compound prepared according to Example 4 of U.S. Patent No. 5,844,026.

N is a hindered amine prepared according to Example 4 of WO 98/54175.

O is 5-chloro-2-(2-hydroxy-3-α-cumyl-5-tert-octylphenyl-2H-benzotriazole.

P is a hindered amine prepared according to Example 1 of WO 98/54177.

These data show that a hindered amine substituted on the N-atom with an alkoxy or cycloalkoxy moiety (Compound K, M or N) in combination with a UV absorber protects the pink scented candle wax far better than conventional UV absorbers. Example 55

Color Fade of Gray Scented Candle Wax under Fluorescent Lamp Exposure

A variety of different stabilizers are evaluated in gray scented candle wax obtained from the Candle-Lite Corporation under fluorescent lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after

Sample^* .wt% add) 29 davs

Blank (no add) 15.72

C (0.3%) 11.57

A (0.3%) 9.88

D (0.15%) +

E (0.15%) 8.01

A (0.15%) +

C (0.15%) 3.20

K (0.15%) +

L (0.15%) 2.54

^*A is octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate, TINUVIN® 384, CIBA. C is bis(1-octyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate, TINUVIN® 123, CIBA). D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA. E is 4-octyloxy-2-hydroxybenzophenone, CHIMMASORB® 81 , CIBA. K is a hindered amine prepared according to Example 1 of WO 98/54175. L is 2,4-bis(biphenyl-4-yl)-6-(2-hydroxy-4-octyloxyphenyl)-s-triazine. These data show that a hindered amine substituted on the N-atom with an alkoxy moiety (Compound K) in combination with an s-triazine UV absorber protects the gray scented candle wax far better than conventional UV absorbers.

Example 56

Color Fade of Gray Scented Candle Wax under UV Lamp Exposure

A variety of different stabilizers are evaluated in white scented candle wax obtained from the Candle-Lite Corporation under UV lamp exposure. The ΔE values represent the change in color after the indicated days of exposure. A low ΔE value indicates less change in color and is highly desired.

ΔE after

Sample^* (wt% add) 23 davs

Blank (no add) 30.07

C (0.3%) 25.70

A (0.3%) 9.14

D (0.15%) +

E (0.15%) 10.96

A (0.15%) +

C (0.15%) 5.11

K (0.15%) +

L (0.15%) 3.50

P (0.15%) +

O (0.15%) 3.93 ^*A is octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate, TINUVIN® 384, CIBA. C is bis(1-octyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate, TINUVIN® 123, CIBA). D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA. E is 4-octyloxy-2-hydroxybenzophenone, CHIMMASORB® 81 , CIBA. K is a hindered amine prepared according to Example 1 of WO 98/54175. L is 2,4-bis(biphenyl-4-yl)-6-(2-hydroxy-4-octyloxyphenyl)-s-triazine. O is 5-chloro-2-(2-hydroxy-3-α-cumyl-5-tert-octylphenyl-2H-benzotriazole. P is the compound prepared according to Example 1 of WO 98/54177.

These data show that a hindered amine substituted on the N-atom with an cycloalkoxy moiety (Compound K or P) in combination with a UV absorber protects the gray scented candle wax far better than conventional UV absorbers.

Example 57

Color Fade of White Scented Candle Wax under Fluorescent Lamp Exposure

ΔE after Sample^* (wt% add. 28 davs

Blank (no add) 34.05

B (0.3%) 31.20

A (0.15%) +

B (0.15%) 29.49 B (0.15%) +

D (0.15%) 24.23

D (0.15%) +

E (0.15%) 20.10

N (0.15%) +

1 (0.15%) 15.46

K (0.15%) +

I (0.15%) 14.02

M (0.15%) +

E (0.15%) 14.79

P (0.15%) +

O (0.15%) 9.44

B is bis(1 ,2,2,6,6-pentamethylpiperidin-4-yl) sebacate, TINUVIN® 292, CIBA.

D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA.

E is 4-octyloxy-2-hydroxybenzophenone, CHIMMASORB® 81 , CIBA.

K is a hindered amine prepared according to Example 1 of WO 98/54175.

M is the compound prepared according to Example 4 of U.S. Patent No. 5,844,026.

N is a hindered amine prepared according to Example 4 of WO 98/54175.

O is 5-chloro-2-(2-hydroxy-3-α-cumyl-5-tert-octylphenyl-2H-benzotriazole.

P is the compound prepared according to Example 1 of WO 98/54177.

These data show that a hindered amine substituted on the N-atom with a cycloalkoxy moiety (Compound P) in combination with a UV absorber protects the white scented candle wax far better than conventional UV absorbers. Example 58

Color Fade of White Scented Candle Wax under UV Lamp Exposure

ΔE after Sample^* (wt% add) 25 davs

Blank (no add) 45.09

B (0.3%) 32.03

A (0.3%) 25.50

A (0.15%) +

B (0.15%) 29.74

D (0.15%) +

E (0.15%) 30.11

P (0.15%) +

O (0.15%) 11.54

^*A is octyl 3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyhydrocinnamate, TINUVIN® 384, CIBA. B is bis(1 ,2,2,6,6-pentamethylpiperidin-4-yl) sebacate, TINUVIN® 292, CIBA. D is 2-(2-hydroxy-5-tert-octylphenyl)-2H-benzotriazole, TINUVIN® 329, CIBA. E is 4-octyloxy-2-hydroxybenzophenone, CHIMMASORB® 81 , CIBA. O is 5-chloro-2-(2-hydroxy-3-α-cumyl-5-tert-octylphenyl-2H-benzotriazole. P is the compound prepared according to Example 1 of WO 98/54177.

These data show that a hindered amine substituted on the N-atom with a cycloalkoxy moiety (Compound P) in combination with a UV absorber protects the white scented candle wax far better than conventional UV absorbers.

Claims

WHAT IS CLAIMED IS:

Claim 1. A composition which comprises

(a) candle wax which is white and unscented; white and scented; dyed and unscented; dyed and scented; dipped and unscented; or dipped and scented, and

(b) an effective stabilizing amount of a combination of

(i) a UV absorber, and

(ii) a hindered amine substituted on the N-atom with an alkoxy, cycloalkoxy or a hydroxy-substituted alkoxy group or mixture of said hindered amines,

wherein the ratio by weight of (i) to (ii) is from 10:1 to 1 :10.

2. A composition according to claim 1 wherein the ratio by weight of (i) to (ii) is from 4:1 to 1 :4.

3. A composition according to claim 1 wherein the effective amount of the UV absorber plus the hindered amine in the candle wax is 0.01 to 10% by weight based on the wax.

4. A composition according to claim 1 wherein the UV absorber of component (i) is a benzotriazole, a benzophenone, an α-cyanoacrylate, an oxanilide, an s-triazine, a cinnamate, a malonate, a benzoate or a salicylate, or a mixture thereof.

5. A composition according to claim 4 wherein the UV absorber is

(a) 4-octyloxy-2-hydroxybenzophenone;

(b) 4-methoxy-2-hydroxybenzophenone;

(c) 2-(2-hydroxy-5-methylphenyl)-2H-benzotriazole; (d) 2-(2-hydroxy-5-tert-octylphenyl-2H-benzotriazole; (e) 2-(2-hydroxy-3,5-di-tert-amylphenyl)-2H-benzotriazole;

(h) 2-(2-hydroxy-5-tert-butylphenyl)-2H-benzotriazole;

(i) 5-chloro-2-(2-hydroxy-3,5-di-tert-butylphenyl)-2H-benzotriazole;

(j) 5-chloro-2-(2-hydroxy-3-tert-butyl-5-methylphenyl)-2H-benzotriazole;

(k) 2-(2-hydroxy-3-sec-butyl-5-tert-butylphenyl)-2H-benzotriazole;

(l) 2-(2-hydroxy-4-octyloxyphenyl)-2H-benzotriazole;

(m) 2-(2-hydroxy-3-dodecyl-5-methylphenyl)-2H-benzotriazole;

(n) 2-[2-hydroxy-3,5-di(α,α-dimethylbenzyl)phenyl]-2H-benzotriazole;

(o) 2-[2-hydroxy-3-(α,α-dimethylbenzyl)-5-tert-octylphenyl]-2H-benzotriazole;

(p) 2-{2-hydroxy-3-tert-butyl-5-[2-(omega-hydroxy-octa(ethyleneoxy)carbonyl)ethyl]- phenyl}-2H-benzotriazole; and

(r) 2-ethylhexyl p-methoxycinnamate;

(s) 4-methoxy-2,2'-dihydroxybenzophenone;

(t) 4,4'dimethoxy-2,2'-dihydroxybenzophenone;

(u) 2,4-bis(2,4-dimethylphenyl)-6-(2-hydroxy-4-octyloxyphenyl)-s-triazine;

(v) 2,4-diphenyl-6-(2-hydroxy-4-hexybxyphenyl)-s-triazine;

(w) 2,4-bis(2,4-dimethylphenyl)-6-[2-hydroxy-4-(3-do-/tri-decyloxy-2-hydroxy propoxy)phenyl]-s-triazine; or

5-α-cumylphenyl]-s-triazine.

6. A composition according to claim 5 wherein the UV absorber is

(a) 4-octyloxy-2-hydroxybenzophenone;

(b) 4-methoxy-2-hydroxybenzophenone;

(d) 2-(2-hydroxy-5-tert-octylphenyl-2H-benzotriazole;

(o) 2-[2-hydroxy-3-(α,α-dimethylbenzyl)-5-tert-octylphenyl]-2H-benzotriazole;

(p) 2-{2-hydroxy-3-tert-butyl-5-[2-(omega-hydroxy-octa(ethyleneoxy)carbonyl)ethyl]- phenyl}-2H-benzotriazole; or

7. A composition according to claim 1 wherein the hindered amine of component (ii) is (a) bis(1-octyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate;

(b) bis(1 -cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate;

(c) 1-cyclohexyloxy-2,2,6,6-tetramethyl-4-octadecylaminopiperidine; (d) 2,4-bis[(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-6-(2- hydroxyethylamino-s-triazine;

(e) bis(1 -cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) adipate;

(f) the oligomeric compound which is the condensation product of 4,4'-hexamethylene- bis(amino-2,2,6,6-tetramethylpiperidine) and 2,4-dichloro-6-[(1 -octyloxy-2,2,6,6-tetra- methylpiperidin-4-yl)butylamino]-s-triazine end-capped with 2-chloro-4,6-bis(dibutyl- amino)-s-triazine;

(h) 1 -methoxy-4-hydroxy-2,2,6,6-tetramethylpiperidine;

(i) 1 -octyloxy-4-hydroxy-2,2,6,6-tetramethylpiperidine;

(j) 1 -cyclohexyloxy-4-hydroxy-2,2,6,6-tetramethylpiperidine;

(k) 1 -methoxy-4-oxo-2,2,6,6-tetramethylpiperidine;

(I) 1 -octyloxy-4-oxo-2,2,6,6-tetramethylpiperidine;

(m) 1 -cyclohexyloxy-4-oxo-2,2,6,6-tetramethylpiperidine,

(n) bis(1 -heptyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate,

(o) bis(1 -nonyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate,

(p) bis(1-dodecyloxy-2,2,6,6-tetramethylpiperidin-4-yl) sebacate, or

(q) N,N',N",N^,"-tetrakis[(4,6-bis(butyl-1-octyloxy-2,2,6,6-pentamethylpiperidin-4-yl)- amino-s-triazin-2-yl]-1 ,10-diamino-4,7-diazadecane.

8. A composition according to claim 1 wherein the hindered amine of component (ii) is

(b) 1-(2-hydroxy-2-methylpropoxy)-4-hydroxy-2,2,6,6-tetramethylpiperidine;

(c) 1-(2-hydroxy-2-methylpropoxy)-4-oxo-2,2,6,6-tetramethylpiperidine;

(f) bis(1 -(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) succinate; (g) bis(1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl) glutarate; or

(h) 2,4-bis{N-[1 -(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-yl]-N- butylamino}-6-(2-hydroxyethylamino)-s-triazine.

9. A composition according to claim 1 wherein component (i) is octyl 3-(benzotriazol-2- yl)-5-tert-butyl-4-hydroxyhydrocinnamate, and component (ii) is bis(1-octyloxy-2,2,6,6- tetramethylpiperidin-4-yl) sebacate.

10. A composition according to claim 1 wherein the composition also includes an antioxidant.

11. A composition according to claim 10 wherein the antioxidant is a phenolic antioxidant, phosphite or hydroxylamine, or mixture thereof.

12. A composition according to claim 10 wherein the effective amount of UV absorber in combination with the hindered amine and an antioxidant is 0.01 to 10% by weight based on the wax.