US3390051A - Dialkylaminocinnamates and dialkylbenzalmalonates in ultraviolet absorbing compositios and methods - Google Patents

Dialkylaminocinnamates and dialkylbenzalmalonates in ultraviolet absorbing compositios and methods Download PDF

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US3390051A
US3390051A US356159A US35615964A US3390051A US 3390051 A US3390051 A US 3390051A US 356159 A US356159 A US 356159A US 35615964 A US35615964 A US 35615964A US 3390051 A US3390051 A US 3390051A
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skin
group
ultraviolet
ultraviolet absorbing
composition
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Baker James Albert
Royal Farnham
James John William
Polkinhorne Harry
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Aspro Nicholas Ltd
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Aspro Nicholas Ltd
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof

Definitions

  • This invention relates to ultraviolet absorbing compositions and is particularly, but not exclusively, concerned with cosmetic sun-screening compositions for topical application to the skin.
  • sunscreening compositions usually in the form of creams or lotions, for topical application, which sunscreening compositions are adapted to or intended to form, deposit or leave on the surface of the skin after application a film comprising a sunscreening agent which will absorb at least the bulk of that portion of the radiation of the sun of a Wavelength between about 290 and 320 m while permitting the passage of at least the bulk of that portion of the ultraviolet range of a wavelength exceeding about 320 m whereby tanning (as opposed to burning) of the subject will not be substantially hindered.
  • an ultraviolet absorbing composition for topical application comprises a dermatologically acceptable liquid or semi- 3,390,951 Patented June 25, 1968 liquid carrier having dissolved or dispersed therein a proportion of at least one dermatologically acceptable compound represented by the general formula:
  • W represents hydrogen or a COZ group
  • Y and Z which may be the same or different, each represent an alkyl group, on 0R group, where R represents hydrogen or an alkyl or alkoxyalkyl group, or an OB group, where B represents a dermatologically acceptable cationic group
  • R and R which may be the same or different, each represent hydrogen or an alkyl or aralkyl group, for example benzyl, or R and R together repre sent a straight or branched chain alkylene group, optional- 1y interrupted by a hetero atom, for example a pyrrolidino, piperidino, morpholino or piperazino group.
  • W in Formula I represents a COZ group
  • R is an alkyl group containing from one to four carbon atoms, such as methyl, ethyl, n-propyl or n-butyl, or a lower alkoxyalkyl group, such as one having the general formula -C H OC H wherein x and y represent integers totalling at least 3, and preferably from 4 to 6, -for example methoxypropyl, ethoxyethyl, n-butoxyethyl or methoxybutyl.
  • B may be, for example, an alkali metal, such as sodium or potassium, or an ammonium group, or an acceptable substituted ammonium group, such as trishydroxyethylarnmonium.
  • R and R both represent alkyl groups having from 1 to 4 carbon atoms, such as methyl, ethyl, n-propyl or n-butyl, and most advantageously one or two carbon atoms.
  • the group is preferably attached to the benzene ring in the para position.
  • R and R which may be the same or different, each represent an alkyl group having from one to four and most advantageously one or two carbon atoms
  • Y represents an 0R group, where R, is an alkyl group having from one to four and most advantageously two or four carbon atoms.
  • R and R which may be the same or different, each represent an alkyl group having from one to four and most advantageously one or two carbon atoms
  • Y and Z which may be the same or different, each represent an R group, where R is an alkyl group having from one to four and most advantageously one or two carbon atoms.
  • a specific example of a compound of the foregoing class is diethyl p-dimethylamino-benzalmalonate.
  • the substituted malonates for use in accordance with the present invention may be made by condensing an appropriate aminobenzaldehyde with an appropriate ester of malonic acid, for example by heating the reactants (conveniently under reflux with provision for the separa tion of formed water) in solution in a mutual solvent in the presence of at least one condensation catalyst, for example piperidine.
  • the desired end product is an acid or a salt
  • the ester may be carefully hydrolysed under alkaline conditions, the acid liberated, and, for a salt, neutralized with the appropriate base.
  • the substituted cinnamates for use in accordance with the present invention may be made by condensing an appropriate aminobenzaldehyde with an appropriate ester of acetic acid in a mutual solvent (conveniently an excess of the ester), in the presence of a condensation catalyst, for example sodium metal or sodium hydride.
  • a condensation catalyst for example sodium metal or sodium hydride.
  • the desired end product is an acid it may be obtained by hydrolysis of the ester, but is better obtained by condensation of the appropriate aminobenzaldehyde with malonic acid in a mutual solvent in the presence of a condensation catalyst such as piperidine.
  • a condensation catalyst such as piperidine.
  • the desired end product is a salt it may be obtained by neutralisation of the acid with an appropriate base.
  • the desired end product contains a primary amino group, the group must be protected during the course of the condensation by an appropriate protecting group, such as acetyl, which is removed by appropriate means at the end of the reaction.
  • novel compounds falling within the definition of Formula I are novel compounds.
  • novel compounds represented by Formula I above the values of W, Y, R and R being chosen so that when R and R are both methyl and the group.
  • W is not hydrogen when Y is a hydroxy or ethoxy group and W is not a carbethoXy group when Y is an ethoxy group.
  • Novel sunscreening compositions such as cosmetic oils, alcoholic solutions, lotions, lipsticks, ornaments, creams and other emulsified products may be prepared with the compounds proposed according to this invention. These compositions may be formulated as cosmetic preparations in otherwise conventional fashion. It is preferred that the should be not only dermatologically but also cosmetically or aesthetically acceptable.
  • compositions containing from 0.5 to 10% by weight of the compounds of this invention Preferably from 0.9 to 3% by weight and most advantageously from 1 to 3% by weight is employed although larger amounts may be used if desired.
  • the optimum proportion to employ will depend particularly on the nature of the coating or film formed or left on the skin, since some types of formulation will permit of the formation of a screen of a greater concentration of screening agent per unit of area than others, depending for example on viscosity, spreading power, and the permanence or otherwise of the vehicle or constituents thereof.
  • novel sunscreening compositions of this invention are not confined to any particular classes of cosmetics or to any particular formulations. Nevertheless, it is preferred to employ the novel compounds of this invention along with a substantially greater amount of a dermatologically acceptable vehicle compatible with the skin, such as corn oil, aqueous ethanol, isopropanol, sesame oil, propylene glycol, benzyl alcohol, oleyl alcohol, isopropyl esters of fatty acids, such as myristic and palmitic acids, or a mineral oil or wax.
  • a dermatologically acceptable vehicle compatible with the skin such as corn oil, aqueous ethanol, isopropanol, sesame oil, propylene glycol, benzyl alcohol, oleyl alcohol, isopropyl esters of fatty acids, such as myristic and palmitic acids, or a mineral oil or wax.
  • the vehicle should be of such a viscosity and/or wetting power that the composition may be satisfactorily applied to the skin as a continuous film
  • an ultraviolet absorbing composition comprises a dermatologically acceptable liquid or semi-liquid carrier having dissolved or dispersed therein at least one compound falling within the definition of Formula I above and also at least one other dermatologically acceptable ultraviolet absorbing compound, whereby the combined effect of the plurality of ultraviolet absorbing compounds enhances the total ultraviolet absorbing properties of films or coatings resulting from or formed by the application of the composition to the skin.
  • the second compound is advantageously one whose ultraviolet absorption is complementary to that of the first ultraviolet absorbing compound whereby the extent of the range and/ or the extent of the amount of ultraviolet radiation absorbed by the film or coating is increased.
  • the first compound shall exert its maximum absorption of ultraviolet light at a wavelength between 320 and 400 mg and the second compound shall exert its maximum absorption thereof at a wavelength between 290 and 320 mg.
  • composition according to this feature of the invention may contain the two compounds in a combined amount of from 0.5 to 10% by weight, and most advantageously from 0.9 to by weight, of the total weight of the composition.
  • the molar ratio of the two compounds one to the other may be from 1:10 to :1, preferably from 5:1 to 1:5 and most advantageously from 2:1 to 1:2.
  • the two compounds and the ratio in which they are employed are such that a 0.5% solution of the compounds (taken in that ratio) in a solvent transparent to ultraviolet radiation (for example ethanol) in a layer 1 cm. thick shall reduce the intensity of all radiation between the wavelengths 290 and 400 mp. which passes into it by at least 90%.
  • a solvent transparent to ultraviolet radiation for example ethanol
  • sunscreening compounds which may be used as the second ultraviolet absorbing component of a composition according to the invention are isobutyl dimethylaminobenzoate, menthyl salicylate and ethoxyethyl and other lower alkoxyalkyl p-methoxycinnamates, particularly such as have at least four, and preferably from four to six carbon atoms, in the alkoxyalkyl group, such as 2-ethoxyethyl p-methoxy-cinnamate.
  • Other suitable sunscreening compounds may, however, be employed, the second such component advantageously being one adapted to absorb in the erythematogenic range as it is normally understood, so complementing the absorption in the tanning range (as it is normally understood) provided by the first component.
  • a difficulty frequently experienced in formulating topical sunscreening compositions is that of securing the presence in an acceptable base or vehicle of a sufiiciently high concentration of the screening agent to provide after application a film or coating the screening contact or power of which will be sufficient to achieve the desired purpose. This is because of the quite limited solubility of many otherwise acceptable screening agents in carrier bases which are acceptable on dermatological and cosmetic grounds.
  • compositions containing at least two distinct screening agents tends to obviate this difficulty to the extent that each agent has its own solubility in the base employed, thus permitting a total concentration of the two agents greater than that which might be obtainable with a single agent, whereby the overall ultraviolet absorption eiiect resulting from the use of the compositions is enhanced not only in the sense that the absorption spectra of the two compounds is complementary, but also to the extent that the ultraviolet absorption spectra of the two compounds so far as they overlap supplements one another.
  • compositions containing at least two distinct screening agents in accordance with one embodiment of the invention is illustrated more clearly in the accompanying drawing which shows in graphic form the ultraviolet absorption of three blackout lotions, the spectra of which were obtained from smears of lotion formulations of the sunscreening agents in a lotion base on silica plates, without drying.
  • Curve 1 was obtained from a lotion containing 1.5% by weight of the known screening agent 2-ethoxyethyl p-methoxy-cinnamate;
  • curve 2 was obtained from a lotion containing 1.5 by weight of a novel screening agentin accordance with the invention, namely isobutyl p-dimethylamino-cinnamate;
  • curve 3 was obtained from a lotion containing 1.5 by weight of each of the screening agents used in the lotions relating to curves 1 and 2. The curves have been adjusted to compensate for variations in thickness between the three smears.
  • the lotion base used in formulating the lotions incorporating the screening agents was as follows:
  • the present invention also provides as a further aspect thereof a method of protecting the skin against erythemaproducing or other undesired ultraviolet radiation, which comprises applying to the skin a film or coating of a composition comprising a cosmetic carrier having disseminated therethrough an effective proportion of one or more ultraviolet absorbing compounds represented by Formula I.
  • the invention is not limited to the protection of the person or parts thereof against erythematogenic radiation since, for example, the invention also finds application in the protection against tanning of normal white persons, such as those who may wish to remain wholly or in part untanned despite exposure to tanning radiation, such as on the grounds of appearance.
  • the invention will find application in those cases where the extent of clothing of the person will vary from time to time and it is desired to avoid the appearance of visible marking as to the extent of dress or undress on a previous occasion under tanning conditions.
  • the invention still further provides a concentrate composition containing at least two ultraviolet absorbing compounds as described above which may be employed in the manufacture of topically applicable compositions according to the invention by incorporation in a suitable proportion in a dermatologically acceptable liquid or semi-liquid carrier.
  • a concentrate composition according to the invention may consist only of the two or more compounds to the extent that they are compatible and/ or the concentrate composition may additionally comprise an extender or diluent material which may ultimately form a component of the ultraviolet absorbing composition or which is more or less readily separable from the mixture of compounds prior to or'on incorporation in the eventual composition, as by evaporation.
  • dermatologically acceptable is used herein to indicate not only that the material or compound referred to is acceptable on strictly dermatological grounds, but also that it is acceptable on other physiological grounds, that is to say that if, for example, the material or compound is absorbed through the skin into the blood-stream, it shall not be toxic in the amounts and by the route it is absorbed.
  • Examples 1 to 6 illustrate the preparation of ultraviolet absorbing compounds which may be used in formulating ultraviolet absorbing compositions in accordance with the invention and Examples 7 to 10 illustrate compositions in accordance with the invention.
  • EXAMPLE 3 Ethyl p-dimethylamino-cinnamate Sodium hydride (7 g. of a 50% dispersion in oil) was added in portions to a cooled, stirred mixture of dimethylaminobenzaldehyde (16.7 g.) and ethyl acetate (200 ml.). After standing overnight, glacial acetic acid was added and excess of ethyl acetate was distilled off in vacuo. The residue was triturated with water, filtered off, dried and crystallized from light petroleum to give the desired compound as a yellow crystalline solid, M.P. 7072 C. Yield 12 g.
  • EXAMPLE 7 Blackout lotion Isopropyl myristate (98 g.) and diethyl p-dimethylamino-benzalmalonate (0.5 g.) were warmed at 50 C. to effect solution of the latter. 2-ethoxyethyl p-methoxycinnamate (0.5 g.) was added and the resulting mixture was cooled to room temperature.
  • Blackout lotion Ingredient Amount, grams (1) Cetyl alcohol 0.5 (2) Stearic acid 3.0 (3) Lanolin 0.5 (4) Mineral oil 5.0 (5) Preservative 0.2 (6) Z-ethoxyethyl p-rnethoxy-cinnamate 2.0 (7) Diethyl p-dimethylamino-benzalmalonate 2.0 (8) Triethanolamine 3.0 (9) Glycerine 3.0 (10) Distilled water 83.3
  • EXAMPLE 9 Blackout cream Ingredient: Amount, grams (1) Mineral oil 5.0 (2) Lanolin 0.5 (3) Polyoxyethylene lanolin derivative (Solulan 98 3.0 (4) Glyceryl monostearate S.E. (self-emulsifying) 5 .0 (5) Stearic acid 15.0 (6) Preservative 0.2 (7) 2-ethoxyethyl p-me'thoxycinnamate 2.0 (8) Diethyl p-diniethylaminobenzalmalonate 2.0 (9) Propylene glycol 5.0
  • Ingredients 1 to 8 were homogenised at C. Ingredients 9 and 10 were heated to 80 C. and added to the mixture of ingredients 1 to 8 at this temperature with mechanical stirring while cooling to 35 C. The resulting product was immediately packed in jars.
  • EXAMPLE 10 Blackout lotion Ingredients 1 to 8 were homogenised at 80 C. Ingredients 9 and 10 were heated to 80 C. and added to the mixture of ingredients 1 to 8 at this temperature with mechanical stirring while cooling to 35 C. The resulting cream was immediately packed in jars.
  • the primary sunscreening compound may be replaced by another compound according to the invention having a comparable ultraviolet absorption spectrum and the 2-ethoxyethyl p-methoxycinnamate may likewise be replaced by a comparable known sunscreening agent.
  • blackout loation and blockout cream employed in Examples 7 and 10 are used as referring to the absorption not only of the burning range of the ultraviolet portion of the spectrum, but also of that portion which in the case of normal white persons is regarded as the tanning range.
  • the lotions and creams exemplified are illustrative of the many forms which the compositions of the invention may take; the lotions and cream can be employed in the same fashion as conventional lotions and creams.
  • a dermatologically acceptable liquid or semi-liquid carrier having therein from 0.5 to 10% by weight of at least one dermatologically acceptable ultraviolet absorbing compound of the formula:
  • W represents hydrogen or COZ
  • Y and Z which may be the same or different, each represent R where R is hydrogen, alkyl of from 1 to 4 carbons or represent 0B where B is a dermatologically acceptable group selected from alkali metal, ammonium and substituted ammonium; and R and R which may be the same or different, each represent alkyl of from 1 to 4 carbons, said composition being such as to form on topical application a continuous film or coating on the skin, and wherein there is also present in the composition an effective amount of at least one other dermatologically acceptable ultraviolet absorbing compound which is effective at a wavelength between 290 and 320 mu.
  • composition as claimed in claim 2 wherein the dermatologically acceptable compounds are present in a molar ratio of one compound to the other of from 1:10 to :1.
  • Method of protecting the skin against erythemaproducing or other undesired ultraviolet radiation which comprises applying to the skin a film or coating of a composition comprising a cosmetic carrier having disseminated therethrough an effective proportion of at least one dermatologically acceptable ultraviolet absorbing compound of the formula:
  • W represents hydrogen or COZ
  • Y and Z which may be the same or different, each represent 0R
  • R is hydrogen, alkyl of from 1 to 4 carbons or represent OB
  • B is a dermatologically acceptable group selected from alkali metal, ammonium and substituted ammonium
  • R and R which may be the same or different, each represent alkyl of from 1 to 4 carbons.
  • a dermatologically acceptable liquid or semi-liquid carrier having therein an effective amount of the dermatologically acceptable ultraviolet absorbing compound triethanolamine p-dimethylaminocinnamate which forms on topical application a continuous film or coating on the skin.
  • Method of protecting the skin against erythemaproducing or other undesired ultraviolet radiation which comprises applying to the skin a film or coating of a composition comprising a cosmetic carrier having disseminated therethrough an effective proportion of diethyl p-dimethylaminobenzalmalonate.
  • Method of protecting the skin against erythema-producing or other undesired ultraviolet radiation which comprises applying to the skin a film or coating of a composition comprising a cosmetic carrier having disseminated therethrough an effective proportion of triethanolamine p-dimethylaminocinnamate.
  • Method of protecting the skin against erythemaproducing or other undesired ultraviolet radiation which comprises applying to the skin a film or coating of a composition comprising a cosmetic carrier having disseminated therethrough an effective proportion of p-dimethylamino-cinnamic acid.
  • Method of protecting the skin against erythemaproducing or other undesired ultraviolet radiation which comprises applying to the skin a film or coating of a composition comprising a cosmetic carrier having disseminated therethrough an effective proportion of di-isobutyl p-dimethylamino-benzalmalonate.
  • Method of protecting the skin against erythemaproducing or other undesired ultraviolet radiation which comprises applying to the skin a film or coating of a composition comprising a cosmetic carrier having dissemintaed therethrough an effective proportion of isobutyl p-dimethylamino-cinnamate.
  • Method of protecting the skin against erythemaproducing or other undesired ultraviolet radiation which comprises applying to the skin a film or coating of a composition comprising a cosmetic carrier having disseminated therethrough an effective proportion of ethyl pdimethylamino-cinnamate.
  • W represents hydrogen or COZ
  • Y and Z which may be the same or different, each represent 0R where R is hydrogen, alkyl of from 1 to 4 carbons or represent OB where B is a dermatologically acceptable group selected from alkali metal, ammonium and substituted ammonium and R and R which may be the same or different, each represent alkyl of from 1 to 4 carbons and wherein there is also present in the composition at least one other dermatologically acceptable ultraviolet absorbing compound which exerts effective absorption of ultraviolet light at a wavelength between 290 and 320 mg.
  • Method of protecting the skin. against erythemaproducing or other undesired ultraviolet radiation which comprises applying to the skin a film or coating of a composition comprising a cosmetic carrier having disseminated therethrough an effective proportion of at least one dermatologically acceptable ultraviolet absorbing compound of the formula:
  • Y is CR wherein R is alkyl of from 1 to 4 carbons and R and R which may be the same or different, each represent alkyl of from 1 to 4 carbons and the salts thereof selected from the group consisting of alkali metal, ammonium and substituted ammonium.
  • Method of protecting the skin against erythemaproducing or other undesired ultraviolet radiation which comprises applying to the skin a film or coating of a composition comprising a cosmetic carrier having disseminatedtherethrough an effective proportion of at least one dermatologically acceptable ultraviolet absorbing of the formula:

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US356159A 1963-04-03 1964-03-31 Dialkylaminocinnamates and dialkylbenzalmalonates in ultraviolet absorbing compositios and methods Expired - Lifetime US3390051A (en)

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3692819A (en) * 1969-09-29 1972-09-19 Ciba Geigy Corp Tertiary aminoacids
US3860598A (en) * 1971-11-09 1975-01-14 Bayer Ag Process for the production of benzylidene compounds
US3992356A (en) * 1972-06-29 1976-11-16 Societe Anonyme Dite: L'oreal Anti-solar polymers and copolymers from vinyloxycarbonyl-methyl 4-N,N-dimethylamino benzoate and vinyloxycarbonyl-methyl-4-methoxy cinnamate monomeas, method of making the same and cosmetic compositions containing the same
US4592906A (en) * 1984-02-14 1986-06-03 Graesser Laboratories, Ltd. Ultra-violet absorbing compounds and compositions containing said compounds
US5237089A (en) * 1986-02-07 1993-08-17 Basf Aktiengesellschaft Nitro or amino substituted phenylalkyl or phenylalkenyl carboxylic acid derivatives
US11472943B2 (en) 2017-07-26 2022-10-18 Mitsui Chemicals, Inc. Polymerizable composition for optical material, optical material, and application thereof

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2652034A1 (de) * 1976-11-15 1978-05-24 Basf Ag Lichtschutzmittel
DE100651T1 (de) * 1982-08-03 1984-07-19 Van Dyk & Co. Inc., Belleville, N.J. Dialkylmalonate als organische hilfsmittel fuer sonnenschutzmittel.
FR2540380B1 (fr) * 1983-02-03 1986-02-07 Oreal Composition cosmetique pour la protection contre le rayonnement ultraviolet et son utilisation a cet effet
WO1988002251A1 (en) * 1986-09-26 1988-04-07 Ici Australia Operations Proprietary Limited Sunscreen compositions and compounds for use therein
NZ221849A (en) * 1986-09-26 1990-09-26 Ici Australia Operations Sunscreen compositions containing tetrahydropyridines
FR2744721B1 (fr) 1996-02-12 1999-06-18 Oreal Nouveaux derives insolubles de s-triazine, leur procede de preparation, compositions les contenant et leurs utilisations

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2798881A (en) * 1954-11-12 1957-07-09 Du Pont 4-(aminoaryl)-1, 3-butadiene-2-carbonitriles and their preparation

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2798881A (en) * 1954-11-12 1957-07-09 Du Pont 4-(aminoaryl)-1, 3-butadiene-2-carbonitriles and their preparation

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3692819A (en) * 1969-09-29 1972-09-19 Ciba Geigy Corp Tertiary aminoacids
US3860598A (en) * 1971-11-09 1975-01-14 Bayer Ag Process for the production of benzylidene compounds
US3992356A (en) * 1972-06-29 1976-11-16 Societe Anonyme Dite: L'oreal Anti-solar polymers and copolymers from vinyloxycarbonyl-methyl 4-N,N-dimethylamino benzoate and vinyloxycarbonyl-methyl-4-methoxy cinnamate monomeas, method of making the same and cosmetic compositions containing the same
US4592906A (en) * 1984-02-14 1986-06-03 Graesser Laboratories, Ltd. Ultra-violet absorbing compounds and compositions containing said compounds
US5237089A (en) * 1986-02-07 1993-08-17 Basf Aktiengesellschaft Nitro or amino substituted phenylalkyl or phenylalkenyl carboxylic acid derivatives
US11472943B2 (en) 2017-07-26 2022-10-18 Mitsui Chemicals, Inc. Polymerizable composition for optical material, optical material, and application thereof

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DE1492274A1 (de) 1969-11-06
GB1064116A (en) 1967-04-05
DK114645B (da) 1969-07-21

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