EP1149081A1 - Aryloxy-poly(oxyalkylen)naphthalimid-derivate als färbemittel - Google Patents

Aryloxy-poly(oxyalkylen)naphthalimid-derivate als färbemittel

Info

Publication number
EP1149081A1
EP1149081A1 EP99973669A EP99973669A EP1149081A1 EP 1149081 A1 EP1149081 A1 EP 1149081A1 EP 99973669 A EP99973669 A EP 99973669A EP 99973669 A EP99973669 A EP 99973669A EP 1149081 A1 EP1149081 A1 EP 1149081A1
Authority
EP
European Patent Office
Prior art keywords
poly
colorant
oxyalkylene
colorants
aryloxy
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP99973669A
Other languages
English (en)
French (fr)
Other versions
EP1149081A4 (de
Inventor
Robert L. Mahaffey, Jr.
James M. Spry
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Milliken and Co
Original Assignee
Milliken and Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US09/243,056 external-priority patent/US5935272A/en
Priority claimed from US09/241,580 external-priority patent/US5998621A/en
Application filed by Milliken and Co filed Critical Milliken and Co
Publication of EP1149081A1 publication Critical patent/EP1149081A1/de
Publication of EP1149081A4 publication Critical patent/EP1149081A4/de
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/40Dyes ; Pigments
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B57/00Other synthetic dyes of known constitution
    • C09B57/08Naphthalimide dyes; Phthalimide dyes

Definitions

  • This invention relates to colorants comprising naphthalimide base groups with
  • naphthalimides are useful as fluorescent colorants, particularly within other liquid
  • aqueous media such as liquid detergents, and the like.
  • naphthalimide-based colorants including U.S. Patents Re. 35,370, to Henry, Re.
  • Lewis et al. 5,308,773, to Lewis et al., 5,357,782, to Henry, 5,420,136, to Lewis et
  • patentee's colorants all exist as solids at room temperature and thus
  • naphthalimide colorant compounds which comprise aryloxy-poly(oxyalkylene)
  • Liquid household compositions such as detergents, fabric softeners,
  • compositions have been commercialized in the past as well, the modern consumer
  • Such a colorant provides for very bright fluorescing colorations
  • colorants are solid in nature they must first be dispersed within liquid media through
  • non-water-soluble naphthalimide colorants exist as waxes or
  • compositions There is no teaching nor fair suggestion within the pertinent art which even alludes to a naphthalimide colorant which can be adapted for use in different
  • object of this invention to provide an aryloxy-poly(oxyalkylene)-derivative
  • the invention is to provide an aryloxy-poly(oxyalkylene) naphthalimide precursor to
  • Yet another object of this invention is to provide a relatively
  • compositions such as, for
  • a household composition i.e., liquid detergent, fabric softener, etc.
  • liquid detergent i.e., liquid detergent, fabric softener, etc.
  • aryloxypolyoxyalkylene naphthalimide derivative colorant to protect uranine
  • the present invention encompasses water-soluble naphthalimide derivative
  • ambient it is meant within a range of from about 20-25°C
  • subject colorant may also be present but only in minimal amounts. Furthermore, the subject colorant may also be present but only in minimal amounts. Furthermore, the subject colorant may also be present but only in minimal amounts. Furthermore, the subject colorant may also be present but only in minimal amounts. Furthermore, the subject colorant may also be present but only in minimal amounts. Furthermore, the subject colorant may also be present but only in minimal amounts. Furthermore, the subject colorant may also be present but only in minimal amounts. Furthermore, the
  • inventive liquid compounds are readily soluble within myriad compositions, including
  • inventive compounds provide excellent fluorescing and coloring
  • colorant compounds can be utilized in applications where standard naphthalimide
  • inventive colorants can be utilized over a wide pH range and
  • fragrances and preservatives are compatible with fragrances and preservatives, as merely examples, without
  • the present invention also encompasses certain compositions comprising
  • compositions are water-based, the colorants of the inventive compositions will not
  • fluorescent colorants such as uranine, are not compatible within such low pH
  • compositions encompassed within this invention include, but are not limited
  • liquid household detergents and cleaners for laundry, dishwashing, light duty
  • compositions include both gel and liquid compositions. Such compositions require at least one
  • compositions comprise tensoactives and water. These compounds are present in order to improve the ability of the composition to clean or remove, soil, stains, and the like, and may
  • anionic surfactants cationic surfactants, amphoteric surfactants, zwitterionic
  • Possible cationic surfactants include quaternary ammonium salts, amines,
  • Suitable amphoterics include mixed C 8 amphocarboxylates,
  • betaine derivatives of quaternary ammonium, phosphonium, and sulfonium
  • duty liquids, tensoactives are present from about 0.01 to about 25% by weight of the
  • liquid detergents from about 0.1 to about 30% by weight; for
  • heavy duty detergents from about 2 to about 75% by weight, and so on.
  • perfumes such as smectite clays,
  • the primary constituent of the aforementioned cleaning compositions is water
  • propylene glycol monomethyl ether dipropylene glycol monomethyl ether, propylene
  • compositions of this invention may only comprise solvents other than
  • liquid cleaning compositions can be found in various United States
  • compositions all comprise well known fabric softening formulations and
  • composition of the present invention would include from about 3 to about 50%> by
  • cationic fabric softening compound preferably a quaternary ammonium compound.
  • the counterion may be a halide, such as fluoride, chloride, bromide, or iodide.
  • counterions may be employed such as methylsulfate, ethylsulfate, hydroxide, acetate,
  • the counterion is chloride or
  • compositions of the present invention Generally, concentrated liquid fabric softener
  • compositions of the present invention can contain 17%) to 50%> solids.
  • fabric softening compositions of the present invention can be prepared according to
  • cationic quaternary ammonium salts include, but are not limited
  • Acyclic quaternary ammonium salts having at least two C 8 - 30 ,
  • C I2 - 22 alkyl chains such as: ditallowdimethyl ammonium chloride
  • Diamido quaternary ammonium salts such as: methyl-
  • Biodegradable quaternary ammonium salts such as N,N-di(tallowoyl-
  • ammonium salts the pH of the composition is adjusted to between about 2 and 7,
  • Biodegradable cationic diester compounds may be employed of the type which have the
  • each R is a short chain C,. 6 , preferably C,. 3 , alkyl or hydroxyalkyl group, e.g.,
  • each R 2 is a long chain C 10 . 22 hydrocarbyl, or substituted hydrocarbyl
  • X " can be any softener-compatible anion, for example, chloride, bromide,
  • the fabric softening compositions of the present invention comprise a water
  • organic solvents such as lower alcohols, which can improve handling, fluidity, and viscosity. From 3 to about 50%>
  • the total composition comprises the active softening compounds
  • the fabric softeners are acyclic quaternary ammonium
  • compositions may be other non-cationic fabric conditioning
  • aminoethylethanolamine carboxylic acids having from 8 to 30 carbon atoms and one
  • esters of polyhydric alcohols such as sorbitan esters or glyceryl stearate, fatty alcohols, ethoxylated fatty alcohols, alkylphenols,
  • ethoxylated diglycerides ethoxylated diglycerides, ethoxylated fatty amines, mineral oils, and polyols, such as
  • inventive fabric softening composition to below about 7.0, preferably in the range
  • the inventive colorant is added in an amount from about 0.001 to about 3.0%
  • additives may be present in amounts from about 0.1 to about
  • These additives include silicones, predominantly polydimethylsiloxanes; soil
  • release polymers such as block copolymers of polyethylene oxide and terephthalate
  • surfactants and nonionic surfactants.
  • Such surfactants and soaps mirror those
  • polymer additives may be any suitable additives discussed above in the cleaning compositions. Additionally, polymer additives may be any suitable additives.
  • Electrolytes may be present, such as guar gum, polyethylene oxide, and cyclodextrin. Electrolytes may be present, such as guar gum, polyethylene oxide, and cyclodextrin. Electrolytes may be present, such as guar gum, polyethylene oxide, and cyclodextrin. Electrolytes may be present, such as guar gum, polyethylene oxide, and cyclodextrin. Electrolytes may
  • Such electrolytes include calcium chloride, magnesium chloride,
  • Preservatives such as glutaraldehyde and formaldehyde may also be added, as
  • Liquid fabric softening compositions encompassed within this invention can be any liquid fabric softening compositions encompassed within this invention.
  • a softening active premix is
  • the colorant can be any colorant, to which is added, with stirring, hot water.
  • the colorant can be any colorant.
  • the colorant is added to the hot water prior to addition to the premix.
  • colorants of invention are highly water soluble
  • inventive colorants may also be present in composition with a solvent.
  • propylene glycol monomethyl ether dipropylene glycol monomethyl ether, propylene
  • glycol o-benzyl-4-chlorophenol
  • deodorized kerosene odorless mineral spirits
  • pine oil n-methyl-pyrrolidone
  • wax n-methyl-pyrrolidone
  • wax n-methyl-pyrrolidone
  • d-limonene methylglycol
  • terpenes terpenes, and white spirits.
  • compositions of this invention may comprise non-aqueous solvents (with no
  • compositions include paint
  • solvent/colorant compositions may be merely utilized as colorant concentrates or
  • compositions such as fabric softener and/or cleaning compositions.
  • inventive colorant would be any colorant.
  • composition preferably from about 0.005 to about 1.0%>; more preferably from about
  • dispersant or dispersants
  • stabilizers including stabilizers, anti-corrosion agents, other surfactants, other dyes
  • naphthalic acid anhydride available from Aceto Corporation. The mixture was
  • a light duty liquid detergent was produced having the following typical
  • Such a composition included an amount of colorant sufficient to give a color depth
  • dimethylammonium chloride softener compound in an amount of about 0.017%) by
  • the resultant composition exhibited a bright yellow
  • Such a composition included an amount of colorant sufficient to give a color depth equal to a commercial sample containing uranine alone as the
  • composition was first analyzed for the initial maximum absorbance at the particularly
  • Test Method 16E Water-Cooled Xenon- Arc Lamp, Continuous Light.
  • COMPOSITION was placed in a sealed transparent plastic bottle and exposed to
  • compositions of EXAMPLE 4 was then also tested for their lightfastness
  • This commercial composition contains both uranine and D&C Yellow
  • compositions were subjected to the same accelerated
  • composition comprising uranine alone as well as the commercially available
  • inventive compositions are novel compositions.
  • the effective shelf-life of the inventive colored compositions are the inventive compositions.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Detergent Compositions (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
EP99973669A 1999-02-02 1999-11-17 Aryloxy-poly(oxyalkylen)naphthalimid-derivate als färbemittel Withdrawn EP1149081A4 (de)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US243056 1988-09-09
US09/243,056 US5935272A (en) 1999-02-02 1999-02-02 Compositions comprising aryloxypolyoxyalkylene naphthalimide derivative colorants
US241580 1999-02-02
US09/241,580 US5998621A (en) 1999-02-02 1999-02-02 Aryloxy-poly(oxyalkylene) naphthalimide derivative colorants
PCT/US1999/026228 WO2000046205A1 (en) 1999-02-02 1999-11-17 Aryloxy-poly(oxyalkylene) naphthalimide derivative colorants

Publications (2)

Publication Number Publication Date
EP1149081A1 true EP1149081A1 (de) 2001-10-31
EP1149081A4 EP1149081A4 (de) 2002-05-29

Family

ID=26934415

Family Applications (1)

Application Number Title Priority Date Filing Date
EP99973669A Withdrawn EP1149081A4 (de) 1999-02-02 1999-11-17 Aryloxy-poly(oxyalkylen)naphthalimid-derivate als färbemittel

Country Status (5)

Country Link
EP (1) EP1149081A4 (de)
JP (1) JP3993747B2 (de)
KR (1) KR100582321B1 (de)
AU (1) AU1470300A (de)
WO (1) WO2000046205A1 (de)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE20216573U1 (de) * 2002-10-27 2004-03-04 Dalli-Werke Wäsche- und Körperpflege GmbH & Co. KG Portion eines gefärbten, nicht festen Waschmittels
EP2844687B1 (de) * 2012-05-02 2018-11-07 Lubrizol Advanced Materials, Inc. Aromatische dispergiermittelzusammensetzung
JP6642940B2 (ja) * 2012-05-02 2020-02-12 ルブリゾル アドバンスド マテリアルズ, インコーポレイテッド 芳香族分散剤組成物
KR102247503B1 (ko) * 2013-11-01 2021-04-30 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 방향족 분산제 조성물
WO2015171592A1 (en) * 2014-05-06 2015-11-12 Milliken & Company Laundry care compositions
CN106187892B (zh) * 2016-07-13 2019-03-15 电子科技大学 一种有机掺杂型双功能器件及其制备方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4992204A (en) * 1989-08-22 1991-02-12 Miliken Research Corporation Irradiation detection and identification method and compositions useful therein
EP0527649A2 (de) * 1991-08-13 1993-02-17 Milliken Research Corporation Poly(oxyalkylen)-substituierter Xanthenfarbstoff und Verfahren zu seiner Herstellung
US5565551A (en) * 1992-03-19 1996-10-15 Microbiomed Corporation Non-azo naphthalimide dyes and uses for same

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4832177B1 (de) * 1970-04-06 1973-10-04
CS193650B1 (en) * 1978-06-30 1979-11-30 Josef Dolezal Brilliant yellow dispersive dyes

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4992204A (en) * 1989-08-22 1991-02-12 Miliken Research Corporation Irradiation detection and identification method and compositions useful therein
EP0527649A2 (de) * 1991-08-13 1993-02-17 Milliken Research Corporation Poly(oxyalkylen)-substituierter Xanthenfarbstoff und Verfahren zu seiner Herstellung
US5565551A (en) * 1992-03-19 1996-10-15 Microbiomed Corporation Non-azo naphthalimide dyes and uses for same

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO0046205A1 *

Also Published As

Publication number Publication date
AU1470300A (en) 2000-08-25
JP2002536464A (ja) 2002-10-29
EP1149081A4 (de) 2002-05-29
WO2000046205A1 (en) 2000-08-10
KR100582321B1 (ko) 2006-05-22
KR20010101949A (ko) 2001-11-15
JP3993747B2 (ja) 2007-10-17

Similar Documents

Publication Publication Date Title
JP4795341B2 (ja) 効率の良い色相染料を有する洗濯用洗剤組成物
US5089148A (en) Liquid fabric conditioner containing fabric softener and peach colorant
EP2145947B1 (de) Wäschebehandlungsmittel
EP1807496A1 (de) Gewebepflegezusammensetzungen mit farbstoff
US5874396A (en) Rinse added laundry additive compositions having color care agents
JPH11504978A (ja) シリコーンエマルションを含んでなる洗濯洗剤組成物
JPH11504979A (ja) 陽イオン系界面活性剤およびシリコーンエマルションを含んでなる液体洗濯洗剤組成物
US5183580A (en) Liquid fabric conditioner containing fabric softener and green colorant
US5130035A (en) Liquid fabric conditioner containing fabric softener and red dye
US5935272A (en) Compositions comprising aryloxypolyoxyalkylene naphthalimide derivative colorants
EP1149081A1 (de) Aryloxy-poly(oxyalkylen)naphthalimid-derivate als färbemittel
JP2002525440A (ja) 低分子量直線状または環状ポリアミンを含んでなる、濯ぎの際に加える布地保護組成物
CA2232413C (en) Stabilised fabric softening compositions
CA2640760A1 (en) Fabric conditioning compositions
TWI359863B (en) Fabric conditioning compositions
JPH11509588A (ja) 低汚染の水溶性色素を含有する布帛柔軟剤
MXPA98000572A (en) Fabric softeners containing soluble colorants in water for stain reduction
US5998621A (en) Aryloxy-poly(oxyalkylene) naphthalimide derivative colorants
JP4444658B2 (ja) ヘミシアニン赤色着色剤を含む液状の繊維柔軟剤配合物
US5929025A (en) Stabilized fabric softening compositions comprising a fabric softening compound, fatty acid, and perfume
US6593289B1 (en) Liquid fabric softener formulations comprising hemicyanine red colorants
US20030171237A1 (en) Novel non-staining red colorants and liquid fabric softener formulations comprising such non-staining colorants
GB2375356A (en) Cationic fabric softening compositions
MXPA99007993A (en) Rinse added laundry additive compositions having color care agents

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20010810

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

A4 Supplementary search report drawn up and despatched

Effective date: 20020416

AK Designated contracting states

Kind code of ref document: A4

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE

RIC1 Information provided on ipc code assigned before grant

Free format text: 7C 07D 221/06 A, 7C 09B 57/08 B, 7C 11D 3/40 B

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20050405