US3878229A - Sun-screening compounds III - Google Patents
Sun-screening compounds III Download PDFInfo
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- US3878229A US3878229A US465259A US46525974A US3878229A US 3878229 A US3878229 A US 3878229A US 465259 A US465259 A US 465259A US 46525974 A US46525974 A US 46525974A US 3878229 A US3878229 A US 3878229A
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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
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- 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
- A61K8/445—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof aromatic, i.e. the carboxylic acid directly linked to the aromatic ring
Definitions
- Sun-screening compositions containing such compounds and a cosmetically acceptable diluent or carrier, and methods of using such compositions, are also disclosed.
- the present invention relates to sun-screening compositions, methods of using the same and novel sunscreening compounds.
- Ultraviolet radiation on the skin such as from the sun, of a wavelength of 290 3 l 3 mp. is known to produce erythema, particularly in fair skinned subjects.
- ultraviolet radiation of from 315 320 my. to 350 400 mp. promotes a tanning ofthe skin.
- a sun-screening composition must at least remove substantially all of the burning rays, and in many instances a good portion of the tanning rays.
- R, and R are independently straight or branched chain lower alkyl; Y is C C alkylene; R is alkyl of 8 to 18 carbon atoms; X is a cosmetically acceptable monoor divalent anion; and n is l or 2 to provide an electrically neutral compound.
- X is halide, sulfate, phosphate, p-(lower alkyl) benzene sulfonate, benzoates, R COO HOOCR -,COO' or OOCR -,COO*, where R is alkyl of l to 18 carbon atoms and R,-, is alkylene of l to 18 carbon atoms.
- Such compounds show absorption of ultraviolet light in the range of 290 315 my. and have good substantivity on the skin.
- the compounds of formula (I) are water soluble, but the degree of water solubility decreases as the number of carbon atoms in R and/or R and/or R,-, in-
- lower alkyl denotes a univalent saturated branched or straight hydrocarbon chain containing from 1 to 6 carbon atoms. Representative of such lower alkyl groups are thus methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec.butyl, tert.butyl, pentyl, isopentyl, neopentyl, tert.pentyl, hexyl, and the like.
- alkylene of 2 to 6 carbon atoms denotes a divalent saturated straight or branched hydrocarbon obtained by removing a hydrogen atom from the lower alkyl defined above, excluding methyl.
- alkyl of l to 18 carbon atoms and alkyl of 8 to 18 carbon atoms denote a univalent saturatd -.branched or straight hydrocarbon chain containing from I to 18 carbon atoms or 8 to 18 carbon atoms,
- alkyl groups are thus methyl, ethyl, propyl, isopropyl, butyl, isobutyl,
- alkylene of l to 18 carbon atoms and alkylene of 8 to 18 carbon atoms denote a divalent saturated branched or straight hydrocarbon chain obtained by removing a hydrogen atom from the alkyl defined above.
- halide denotes chloride, bromide, iodide and fluoride, preferably chloride or bromide.
- R and R are C -C straight or branched chain alkyl.
- the no carboxylic acid is one wherein R is lower alkylene, and most preferably alkylene of l to 4 carbon atoms.
- Compounds which are active as sun-screening agents are known and include such widely diverse compounds as dibenzylacetone, quinine sulfate and ethyl umbelliferone.
- Alkyl esters of p-dialkylaminobenzoic acid have also been proposed for use as sun-screening agents in US. Pat. Nos. 2,853,423; 3,403,207; and 3,479,428. In view of this highly empirical nature of the ability of a compound selectively to absorb ultraviolet radiation in the narrow range of 290 to 315 mu, it was not expected that the compounds of formula (I) would be useful as sun-screening agents.
- the quaternary salts of formula (I) where X is halide can be prepared by reacting at room temperature, with or without a solvent. approximately stoichiometric quantities of a dialkylaminoalkyl pdialkylaminobenzoate (ll) and an alkyl halide (lll) to form the quaternary ammonium halide (lV according to process (A) below:
- Compounds of formula (I) where X is other than halide can be formed treating the quaternary ammonium halide (IV) with silver oxide to produce the mono quaternary ammonium hydroxide.
- the excess silver oxide and precipitated silver halide is removed by filtration and the aqueous solution of mono-quaternary ammonium hydroxide then is reacted with an appropriate acid to introduce the desired anion, such as sulfonic acid, phosphoric acid, p-(lower alkyl) benzenesulfonic acid, benzoic acid or a monoor dicarboxylic acid of the formula R COO l-l or R (COOH)
- the quaternary ammonium halide (1V) can be reacted with the desired acid in approximately stoichiometric quantities, in accordance with processes (B) or (C).
- dialkylaminoalkyl p-dialkylaminobenzoate (ll) used in process (A) is known, e.g. see US. Pat. No. 820,830, and can conveniently be made by alkylating an alkyl p-aminobenzoate with an alkyl halide in an organic solvent, and reacting the resulting alkyl pdialkylaminobenzoate with a dialkylaminoalkanol.
- dialkylaminoalkyl pdialkylaminobenzoate may be:
- the aliphatic dicarboxylic acid R (COOH)- used in reaction (C) may be malonic acid, succinic acid, adipic acid, 2,2-dimethylglutaric acid, suberic acid, sebacic acid, dodecanedioic acid, tetradecanedioic acid, hexadecanedioic acid, and nonadecanedioic acid.
- the sun-screening agents of formula (I) are applied to the skin in the form of a sun-screen composition
- a sun-screen composition comprising the compound offormula (l) and a cosmetically acceptable diluent or carrier.
- the term .cosmetically acceptable diluent or carrier denotes a nontoxic, non-irritating substance which when mixed with the compound of formula (I) makes the compound more suitable to be appliedto the skin.
- the compositions can thus be solutions, oils, lotions, ointments, liquid or solid creams, aerosols and the like.
- the sun-screening composition of the invention is formed by admixing dissolving or dispersing the sunscreening compound of formula (1) into the desired cosmetically acceptable diluent or carrier.
- Solutions are formed by dissolving the sun-screening compound in water or other solvent.
- Oils are prepared by using vegetable andlor mineral oils, such as sesame oil and/or white mineral oil as the cosmetically acceptable diluent or carrier.
- Creams may be prepared by adding lanolin and a suitable absorbent base to the vegetable and/or mineral oils. Oil-in-water emulsions may be employed as the vehicle to form lotions, but are not preferred since such compositions tend to wash off more easily than others. by
- An alcoholic lotion containing an alcohol, such as ethanol or isopropanol, and a film-forming substance as the cosmetically acceptable diluent or carrier is preferred, since this tends to provide more permanent protection even after exposure of the skin to water.
- Preferred film-forming agents for alcoholic lotions are cator oil, lauryl and oleyl alcohols, glycol and glyceryl oleates, mannitol and sorbitol oleate, laurate or ricinoleate, butyl stearate, ethyl oleate, laurate, or ricinoleate and methyl oleate, laurate or ricinoleate.
- Perfumes, anti-oxidants, colorants. insect-repellants and the like may be included in the sun-screening composition, if desired.
- the sun-screening composition of the invention contains an effective amount of the sun-screening compound of formula (I) to prevent erythema.
- an amount of 0.01 to preferably 0.05 to 3%, by weight, of the total composition, of the sun-screening compound of formula (I) may be used.
- the composition is applied topically every few hours, as needed, in the same manner as conventional sun-screening compositions.
- the compounds of the invention may also be used to protect blond and light-colored hair from the deleterious effects of ultraviolet radiation.
- the compounds of formula (I) are admixed with the cosmetically acceptable diluent or carrier to provide a composition containing from 0.05 to 10%, by weight,-', ,5 preferably 2 to 5%, by weight, of the compound of formula (l).
- the hair-protection compositions are applied to the hair in the same manner as a conventional hair lotion, hair cream or hair tonic, before exposure to ultraviolet radiation, and thereafter as desired.
- Cosmetically acceptable diluents or carriers used in such conventional hair preparations may be used in the hairprotection composition of the invention.
- a 2%, by weight, solution of the candidate compound in 50% ethanol-50% water is then rubbed into the skin, dried in air, and part of the air-dried surface is rinsed with water for 2 minutes. Examination of the rinsed and unrised sections of skin was then made in UV (black) light. The retention of the UV absorber on the skin is determined by observing the color of the treated and untreated sections under UV light and comparing the color tothe reference solutions.
- Tests for sunburn protection are carried out by applying a 2%, by weight, solution of the candidate compound in 50% ethanol-50% water to a small patch of skin, followed by exposure to sun for 2 hours.
- a compound must prevent erythema after exposure for 2 hours to the sun at a latitude of New York City.
- TEST PROCEDURE FOR HAlR The substantivity of the candidate compound to hair is tested in the following manner.
- the candidate compound is dissolved in mls. of water to provide a 0.1%, by weight, aqueous solution.
- 10 gms. of hair is immersed in the resulting aqueous solution, stirred for one-half hour, removed, rinsed and dried.
- the UV- absorption of the aqueous solution into which the hair was immersed is measured both before and after the immersion of the hair in the solution, using the same technique described above.
- the of the compound left after rinsing determines the amount of substantivit
- the following Examples illustrate the invention. In the Examples, all percentages and parts are by weight unless stated otherwise.
- compound (B) When the pH of the aqueous solution is adjusted to 8.5, compound (B) has higher substantivity on the skin and gives good protection against sunburn.
- the precipitated product is filtered from the mixture and dried.
- R, and R are independently straight or branched chain lower alkyl; Y is C C alkylene; R is alkyl of 8 to 18 carbon atoms; X is an anion selected CH COO the mixture 3.
- R is straight or branched chain alkyl of ll to 18 carbon atoms.
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Abstract
Sun-screening compounds, useful to protect the skin and hair against deleterious effects upon exposure to ultraviolet radiation, of the formula:
WHERE R1 and R2 are independently straight or branched chain lower alkyl; Y is C2 - C6 alkylene; R3 is alkyl of 8 to 18 carbon atoms; X is a cosmetically acceptable mono- or divalent anion; and n is 1 or 2 to provide an electrically neutral compound. Sun-screening compositions containing such compounds and a cosmetically acceptable diluent or carrier, and methods of using such compositions, are also disclosed.
WHERE R1 and R2 are independently straight or branched chain lower alkyl; Y is C2 - C6 alkylene; R3 is alkyl of 8 to 18 carbon atoms; X is a cosmetically acceptable mono- or divalent anion; and n is 1 or 2 to provide an electrically neutral compound. Sun-screening compositions containing such compounds and a cosmetically acceptable diluent or carrier, and methods of using such compositions, are also disclosed.
Description
United States Patent [191 Strobel [4 1 Apr. 15, 1975 SUN-SCREENING COMPOUNDS in [75] Inventor: Albert Frederick Strobel, Delmar,
[73] Assignee: GAF Corporation, New York, NY.
[22] Filed: Apr. 29, 1974 [21] Appl. No.: 465,259
[52] U.S. Cl. 260/404.5; 260/472; 424/60 [51] Int. Cl. Cllc 3/00 [58] Field of Search 260/404.5, 472
[56] References Cited UNITED STATES PATENTS 3,536,723 10/1970 Ghelardoni et al. 260/472 Primary Examiner-Lorraine A. Weinberger Assistant Examiner-L. A. Thaxton Attorney, Agent, or FirmWalter C. Kehm; Samson B. Leavitt [57] ABSTRACT Sun-screening compounds, useful to protect the skin and hair against deleterious effects upon exposure to ultraviolet radiation, of the formula:
Sun-screening compositions containing such compounds and a cosmetically acceptable diluent or carrier, and methods of using such compositions, are also disclosed.
20 Claims, N0 Drawings SUN-SCREENING COMPOUNDS III The present invention relates to sun-screening compositions, methods of using the same and novel sunscreening compounds.
Ultraviolet radiation on the skin, such as from the sun, ofa wavelength of 290 3 l 3 mp. is known to produce erythema, particularly in fair skinned subjects. On the other hand, ultraviolet radiation of from 315 320 my. to 350 400 mp. promotes a tanning ofthe skin. To be effective, a sun-screening composition must at least remove substantially all of the burning rays, and in many instances a good portion of the tanning rays.
It is, therefore, an object of this invention to provide novel sun-screening compounds that are effective to prevent erythema.
It is a further object of the invention to provide new sun-screening compositions containing the sunscreening compounds of the invention.
These objects are provided by the provision ofa sunscreening compound of formula (l):
where R, and R are independently straight or branched chain lower alkyl; Y is C C alkylene; R is alkyl of 8 to 18 carbon atoms; X is a cosmetically acceptable monoor divalent anion; and n is l or 2 to provide an electrically neutral compound. Preferably, X is halide, sulfate, phosphate, p-(lower alkyl) benzene sulfonate, benzoates, R COO HOOCR -,COO' or OOCR -,COO*, where R is alkyl of l to 18 carbon atoms and R,-, is alkylene of l to 18 carbon atoms. Such compounds show absorption of ultraviolet light in the range of 290 315 my. and have good substantivity on the skin. The compounds of formula (I) are water soluble, but the degree of water solubility decreases as the number of carbon atoms in R and/or R and/or R,-, in-
crease.
The term lower alkyl denotes a univalent saturated branched or straight hydrocarbon chain containing from 1 to 6 carbon atoms. Representative ofsuch lower alkyl groups are thus methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec.butyl, tert.butyl, pentyl, isopentyl, neopentyl, tert.pentyl, hexyl, and the like. The term alkylene of 2 to 6 carbon atoms denotes a divalent saturated straight or branched hydrocarbon obtained by removing a hydrogen atom from the lower alkyl defined above, excluding methyl.
The terms alkyl of l to 18 carbon atoms and alkyl of 8 to 18 carbon atoms denote a univalent saturatd -.branched or straight hydrocarbon chain containing from I to 18 carbon atoms or 8 to 18 carbon atoms,
repsectively. Representative of such alkyl groups are thus methyl, ethyl, propyl, isopropyl, butyl, isobutyl,
sec.butyl, tert.butyl, pentyl, isopentyl, neopentyl, tert.- 5 pentyl, hexyl. isohexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl and the like. The terms alkylene of l to 18 carbon atoms and alkylene of 8 to 18 carbon atoms denote a divalent saturated branched or straight hydrocarbon chain obtained by removing a hydrogen atom from the alkyl defined above.
The term halide denotes chloride, bromide, iodide and fluoride, preferably chloride or bromide.
In a preferred embodiment of the invention, R and R are C -C straight or branched chain alkyl.
It is further preferred to employ compounds in which R is alkyl of l l to 18 carbon atoms, because the more carbon atoms in R the greater the substantivity of the compound of formula (I).
It is further preferred to employ compounds in which the anion, R ,COO is alkyl of 7 to 17 carbon atoms,
where R,, R R and R and n are as defined above, Z is COOH or COO, and n is 1 when Z is COOH and n is 2 when Z is COO. Preferably, the no carboxylic acid is one wherein R is lower alkylene, and most preferably alkylene of l to 4 carbon atoms. Compounds which are active as sun-screening agents are known and include such widely diverse compounds as dibenzylacetone, quinine sulfate and ethyl umbelliferone. Alkyl esters of p-dialkylaminobenzoic acid have also been proposed for use as sun-screening agents in US. Pat. Nos. 2,853,423; 3,403,207; and 3,479,428. In view of this highly empirical nature of the ability of a compound selectively to absorb ultraviolet radiation in the narrow range of 290 to 315 mu, it was not expected that the compounds of formula (I) would be useful as sun-screening agents.
Mono-quaternary ammonium compounds useful as intermediates in the preparation of therapeutic agents have been proposed in US. Pat. No. 2,717,905. So far as we are aware, the sun-screening compounds of formula (l) are novel.
The quaternary salts of formula (I) where X is halide can be prepared by reacting at room temperature, with or without a solvent. approximately stoichiometric quantities of a dialkylaminoalkyl pdialkylaminobenzoate (ll) and an alkyl halide (lll) to form the quaternary ammonium halide (lV according to process (A) below:
(A) R1 R2 N COOY-N R -ha11de R/ \R 3 (11) (III) (-9 2 N-COOY-N R3 halide 1 2 where R R and R are-defined above, and halide is chloride, bromide, iodide or fluoride, preferably chloride or bromide.
Compounds of formula (I) where X is other than halide can be formed treating the quaternary ammonium halide (IV) with silver oxide to produce the mono quaternary ammonium hydroxide. The excess silver oxide and precipitated silver halide is removed by filtration and the aqueous solution of mono-quaternary ammonium hydroxide then is reacted with an appropriate acid to introduce the desired anion, such as sulfonic acid, phosphoric acid, p-(lower alkyl) benzenesulfonic acid, benzoic acid or a monoor dicarboxylic acid of the formula R COO l-l or R (COOH) Alternatively, the quaternary ammonium halide (1V) can be reacted with the desired acid in approximately stoichiometric quantities, in accordance with processes (B) or (C).
(B) R,COOH (W (l where R is as defined above (C) n(HOOC-R P,COOH) (W) (la) where n is l or 2 and R is as defined above.
The dialkylaminoalkyl p-dialkylaminobenzoate (ll) used in process (A) is known, e.g. see US. Pat. No. 820,830, and can conveniently be made by alkylating an alkyl p-aminobenzoate with an alkyl halide in an organic solvent, and reacting the resulting alkyl pdialkylaminobenzoate with a dialkylaminoalkanol.
For use in process (A), the dialkylaminoalkyl pdialkylaminobenzoate may be:
dimethylaminoethyl p-dimethylaminobenzoate diethylaminoethyl p-dipropylaminobenzoate dimethylamioethyl p-dipentlyaminobenzoate di-i-propylaminoethyl p-dihexylaminobenzoate dihexylaminoethyl p-di-i-propylaminobenzoate acid, nor i-valeric acid, caprylic acid, octanoic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid and nonadecanoic acid.
The aliphatic dicarboxylic acid R (COOH)- used in reaction (C) may be malonic acid, succinic acid, adipic acid, 2,2-dimethylglutaric acid, suberic acid, sebacic acid, dodecanedioic acid, tetradecanedioic acid, hexadecanedioic acid, and nonadecanedioic acid.
The following are representative sun-screening compounds of formula (I):
The sun-screening agents of formula (I) are applied to the skin in the form of a sun-screen composition comprising the compound offormula (l) and a cosmetically acceptable diluent or carrier. The term .cosmetically acceptable diluent or carrier" denotes a nontoxic, non-irritating substance which when mixed with the compound of formula (I) makes the compound more suitable to be appliedto the skin. The compositions can thus be solutions, oils, lotions, ointments, liquid or solid creams, aerosols and the like.
The sun-screening composition of the invention is formed by admixing dissolving or dispersing the sunscreening compound of formula (1) into the desired cosmetically acceptable diluent or carrier. Solutions are formed by dissolving the sun-screening compound in water or other solvent. Oils are prepared by using vegetable andlor mineral oils, such as sesame oil and/or white mineral oil as the cosmetically acceptable diluent or carrier. Creams may be prepared by adding lanolin and a suitable absorbent base to the vegetable and/or mineral oils. Oil-in-water emulsions may be employed as the vehicle to form lotions, but are not preferred since such compositions tend to wash off more easily than others. by
An alcoholic lotion containing an alcohol, such as ethanol or isopropanol, and a film-forming substance as the cosmetically acceptable diluent or carrier is preferred, since this tends to provide more permanent protection even after exposure of the skin to water. Preferred film-forming agents for alcoholic lotions are cator oil, lauryl and oleyl alcohols, glycol and glyceryl oleates, mannitol and sorbitol oleate, laurate or ricinoleate, butyl stearate, ethyl oleate, laurate, or ricinoleate and methyl oleate, laurate or ricinoleate.
Perfumes, anti-oxidants, colorants. insect-repellants and the like may be included in the sun-screening composition, if desired.
The sun-screening composition of the invention contains an effective amount of the sun-screening compound of formula (I) to prevent erythema. In general. an amount of 0.01 to preferably 0.05 to 3%, by weight, of the total composition, of the sun-screening compound of formula (I) may be used. The composition is applied topically every few hours, as needed, in the same manner as conventional sun-screening compositions.
The compounds of the invention may also be used to protect blond and light-colored hair from the deleterious effects of ultraviolet radiation. In this case, the compounds of formula (I) are admixed with the cosmetically acceptable diluent or carrier to provide a composition containing from 0.05 to 10%, by weight,-', ,5 preferably 2 to 5%, by weight, of the compound of formula (l). The hair-protection compositions are applied to the hair in the same manner as a conventional hair lotion, hair cream or hair tonic, before exposure to ultraviolet radiation, and thereafter as desired. Cosmetically acceptable diluents or carriers used in such conventional hair preparations may be used in the hairprotection composition of the invention.
In the Examples, the following procedures were used:
TEST PROCEDURE ON SKIN Reference solutions of the candidate compound in 50/50 ethanol-water solvent are prepared in concentrations of 2%, by weight, and below. Such solutions are applied to the skin and dried in air. Examination of the treated section of skin under UV light reveals a bluishwhite color for untreated skin and brownish-black to black color fo treated skin.
A 2%, by weight, solution of the candidate compound in 50% ethanol-50% water is then rubbed into the skin, dried in air, and part of the air-dried surface is rinsed with water for 2 minutes. Examination of the rinsed and unrised sections of skin was then made in UV (black) light. The retention of the UV absorber on the skin is determined by observing the color of the treated and untreated sections under UV light and comparing the color tothe reference solutions.
Tests for sunburn protection are carried out by applying a 2%, by weight, solution of the candidate compound in 50% ethanol-50% water to a small patch of skin, followed by exposure to sun for 2 hours. To be successful, a compound must prevent erythema after exposure for 2 hours to the sun at a latitude of New York City.
TEST PROCEDURE FOR HAlR The substantivity of the candidate compound to hair is tested in the following manner. The candidate compound is dissolved in mls. of water to provide a 0.1%, by weight, aqueous solution. 10 gms. of hair is immersed in the resulting aqueous solution, stirred for one-half hour, removed, rinsed and dried. The UV- absorption of the aqueous solution into which the hair was immersed is measured both before and after the immersion of the hair in the solution, using the same technique described above. The of the compound left after rinsing determines the amount of substantivit The following Examples illustrate the invention. In the Examples, all percentages and parts are by weight unless stated otherwise.
EXAMPLE 1 Preparation and application to the skin of:
C00C H N-CH x, where x Br- (Compound A) or CH C00 (Compound B) 148g. ethyl p-aminobenzoate, 4.5g. ethyl iodide and 600 ml. ethanol were heated in an autoclave for 6 hours at 185C. Then the solvent and excess ethyl iodide were evaporated at C under atmospheric pressure, producingiabout 150g. ethyl p-diethylaminobenzoate.
benzene evaporated to give about 80g. crude dimethylaminoethyl ester of p-dimethylaminobenzoic acid.
26.4g. of this compound was mixed with 21g. bromooctane and 100 ml. isopropanol. The mixture was (H C N I refluxed for 24 hours, and the product evaporated to dryness on a steam bath. Compound (A) was recovered. An aqueous 0.1% solution of compound (A) was applied to skin and afforded protection against sunburn. but allowed tanning.
To a 1% aqueous solution of compound (A) was added sodium acetate (based on the weight of the solution). The compound (B) precipitated, was filtered off and dried.
When 10g. hair was treated with 100 ml. aqueous solution containing 0.1% ofcompound (B), the hair was undue against indue deterioration on exposure to UV light. Substantivity was 75%, obtained by determining the K value of the solution before and after immersion of the hair. It also has similar substantivity and protective properties when applied to skin.
When the pH of the aqueous solution is adjusted to 8.5, compound (B) has higher substantivity on the skin and gives good protection against sunburn.
Maximum absorption of compounds (A) and (B) is at 313 mu.
EXAMPLE 2 Preparation and application to the skin of the compound having the formula:
Q/CHS (H5C2)2N A 0.1% aqueous solution of the Compound (A) of Example 1 was adjusted to pH 7.0 with sodium laurate salt. Skin treated with this preparation was protected against sun-burn. Skin substantivity was excellent. Maximum absorption is at 313 mu.
EXAMPLE 3 Preparation and application to the skin of the compound having the formula:
G/CH3 cooc a N-ca x where x is 5:
c H (Compound C) or X2 5 ca (ca acoo- Compound (D) EXAMPLE 4 Preparation and application to the skin of the product having the formula:
9 2*5 i C000 11 -C'H X whereX is Br 4 a I Compound (E) or CH (CH CHCOO (Compound F) 82.5 g. ethyl p-aminobenzoate. 100 ml. methanol and g. dimethyl sulfate were mixed and gradually heated to C. After 3 hours the charge was treated with 50 g. sodium carbonate to delta paper neutrality. 1t was then treated with 100 ml. benzene and 200 ml. water and the layers separated. The upper layer was evaporated free from benzene to give g. ethyl pdimethylaminobenzoate.
22.1 g. of this product, 0.50 g. sodium methoxide and 50 g. diethylaminoethanol were heated to 140C. for 24 GD/CHS (r1 uooc a u -cn hours while distilling off the ethanol that was liberated. The product was extracted with 200 ml. water and 100 ml. benzene, the water layer removed and the benzene evaporated from the water layer to give about 80 g. crude diethylaminoethyl ester 0 of pdimethylaminobenzoic acid.
This product was then mixed with 32 g. bromooctadecane and 100 ml. isopropanol. The mixture was refluxed for 24 hours, and the product evaporated to dryness on a stream bath to give Compound (E).
An aqueous 0.1% solution of Compound (E) was adjusted to pH 7.0 with sodium Z-ethylhexoate to produce Compound (F), which was highly skin substantive and afforded excellent protection against sun-burning.
EXAMPLE 5 In the manner of Example 2, to a 1% aqueous solution of Compound (A) was added sodium stearate to form:
is treated with half the equimolar amount of the disodium salt'of succinic acid to give CH COO 1:25
The precipitated product is filtered from the mixture and dried.
I EXAMPLE 7 An aqueous 0.1% solution of EB ca s z 2 N 000 H m ca 2 4 3 122s was treated with an equimolar amount of the monosodium salt of succinic acid cu COONa ca coou I The precipitated product is filtered from and dried.
1 claim: 1. A compound of the formula:
N I COOY-N-R X wherein' R, and R are independently straight or branched chain lower alkyl; Y is C C alkylene; R is alkyl of 8 to 18 carbon atoms; X is an anion selected CH COO the mixture 3. The compound according to claim 1, wherein R is straight or branched chain alkyl of ll to 18 carbon atoms.
12. The compound according to claim 1, which is CH ca coo CO0C2H4N\CH3 3 tu c a 13. The compound according to claim 1, which is 4. The compound according to claim 1, wherein X is halide.
5. The compound according to claim 1, wherein X is R COO' and n is l.
6. The compound according to claim 5, wherein R is alkyl or 7 to 17 carbon atoms.
7. The compound according to claim 1, wherein X is HOOCR -,COO and n is l.
8. The compound according to claim 7, wherein R is lower alkylene.
9. The compound according to claim 1, wherein X is OOC-COO and n is 2.
10. The compound according to claim 9, wherein R,-, is lower alkylene.
11. The compound according to claim 1. which is H 6) CH3 Br C N COOC H N CH 14. The compound according to claim 1, which is 15. The compound according to claim 1, which is 16. The compound according to claim 1, which is 17. The compound according to claim 1, which is 19- The mpoun accordi g to Claim which is (H O) N COOC H C H5 18 37 I c H \2 5 ca (crr cncoo 18. The compound according to claim 1, which is 20. The compound according to clairn l, which is 6/ 3 (H C 2 COOC H N CH C H COO (2 3 CH COOH
Claims (20)
1. A COMPOUND OF THE FORMULA:
2. The compound according to claim 1, wherein R1 and R2 are straight or branched chain alkyl of 1 to 3 carbon atoms.
3. The compound according to claim 1, wherein R3 is straight or branched chain alkyl of 11 to 18 carbon atoms.
4. The compound according to claim 1, wherein X is halide.
5. The compound according to claim 1, wherein X is R4-COO and n is 1.
6. The compound according to claim 5, wherein R4 is alkyl or 7 to 17 carbon atoms.
7. The compound according to claim 1, wherein X is HOOC-R5-COO and n is 1.
8. The compound according to claim 7, wherein R5 is lower alkylene.
9. The compound according to claim 1, wherein X is OOC-COO and n is 2.
10. The compound according to claim 9, wherein R5 is lower alkylene.
11. The compound according to claim 1, which is
12. The compound according to claim 1, which is
13. The compound according to claim 1, which is
14. The compound according to claim 1, which is
15. The compound according to claim 1, which is
16. The compound according to claim 1, which is
17. The compound according to claim 1, which is
18. The compound according to claim 1, which is
19. The compound according to claim 1, which is
20. The compound according to claim 1, which is
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US465259A US3878229A (en) | 1974-04-29 | 1974-04-29 | Sun-screening compounds III |
| CA217,454A CA1064049A (en) | 1974-04-29 | 1975-01-07 | Salts of alkanolamine esters of para dialkylaminobenzoic acid and their use as sun-screening agents |
| GB82975A GB1428648A (en) | 1974-04-29 | 1975-01-08 | Quaternary compounds of dialkyl benzoic derivatives sun- screening compositions containing the compounds and their appli cation as sun-screening agents |
| JP50013932A JPS50140642A (en) | 1974-04-29 | 1975-01-31 | |
| DE19752509647 DE2509647A1 (en) | 1974-04-29 | 1975-03-05 | NEW DERIVATIVES OF DIALKYLAMINOALKYL- P-DIALKYL-AMINOBENZOAEUREESTERS |
| CH288275A CH616842A5 (en) | 1974-04-29 | 1975-03-06 | |
| FR7513032A FR2268789B1 (en) | 1974-04-29 | 1975-04-25 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US465259A US3878229A (en) | 1974-04-29 | 1974-04-29 | Sun-screening compounds III |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3878229A true US3878229A (en) | 1975-04-15 |
Family
ID=23847063
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US465259A Expired - Lifetime US3878229A (en) | 1974-04-29 | 1974-04-29 | Sun-screening compounds III |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3878229A (en) |
| JP (1) | JPS50140642A (en) |
| CA (1) | CA1064049A (en) |
| CH (1) | CH616842A5 (en) |
| DE (1) | DE2509647A1 (en) |
| FR (1) | FR2268789B1 (en) |
| GB (1) | GB1428648A (en) |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU569940B2 (en) * | 1984-06-21 | 1988-02-25 | Van Dyk & Company | Benzene sulfonate quaternary ammonium salts of sunscreen carboxylic acids |
| US5427774A (en) * | 1993-08-25 | 1995-06-27 | Isp Van Dyk Inc. | Heterocyclic quaternary salts of para-dialkylamino benzamide derivatives |
| US5474691A (en) * | 1994-07-26 | 1995-12-12 | The Procter & Gamble Company | Dryer-added fabric treatment article of manufacture containing antioxidant and sunscreen compounds for sun fade protection of fabrics |
| US5543083A (en) * | 1994-07-26 | 1996-08-06 | The Procter & Gamble Company | Fatty amine derivatives of butylated hydroxy toluene for the protection of surfaces from physical and chemical degradation |
| US5705474A (en) * | 1994-07-26 | 1998-01-06 | The Procter & Gamble Company | Rinse added fabric softener compositions containing sunscreens for sun-fade protection for fabrics |
| US5723435A (en) * | 1994-07-26 | 1998-03-03 | The Procter & Gamble Company | Rinse added fabric softener compositions containing antioxidants for sun-fade protection fabrics |
| US6607735B2 (en) | 2000-12-21 | 2003-08-19 | Johnson & Johnson Consumer Companies, Inc. | Method for reducing the appearance of dark circles under the eyes |
| US20040191206A1 (en) * | 2000-10-02 | 2004-09-30 | Curtis Cole | Methods for reduction of inflammation and erythema |
| US20040213754A1 (en) * | 2000-10-02 | 2004-10-28 | Cole Curtis A. | Method for cleansing sensitive skin using an alkanolamine |
| US20050238730A1 (en) * | 2001-11-21 | 2005-10-27 | Agnes Le Fur | Compositions comprising an ethanolamine derivative and organic metal salts |
| US20080063844A1 (en) * | 2001-06-29 | 2008-03-13 | Mannington Mills, Inc. | Surface coverings containing aluminum oxide |
| US7396526B1 (en) | 1998-11-12 | 2008-07-08 | Johnson & Johnson Consumer Companies, Inc. | Skin care composition |
| CN109232285A (en) * | 2018-10-16 | 2019-01-18 | 新乡学院 | A kind of synthetic method and application of the benzocainum disubstituted derivative with antibacterial activity |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59140694A (en) * | 1983-01-31 | 1984-08-13 | Sharp Corp | Refresh method of dynamic ram |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3536723A (en) * | 1966-09-27 | 1970-10-27 | Menarini Soc In Accomandita Se | P - (2 - alkyloxy - benzoyl) - aminobenzoates of n - dialkylamine - alkyl and their quaternary salts |
-
1974
- 1974-04-29 US US465259A patent/US3878229A/en not_active Expired - Lifetime
-
1975
- 1975-01-07 CA CA217,454A patent/CA1064049A/en not_active Expired
- 1975-01-08 GB GB82975A patent/GB1428648A/en not_active Expired
- 1975-01-31 JP JP50013932A patent/JPS50140642A/ja active Pending
- 1975-03-05 DE DE19752509647 patent/DE2509647A1/en not_active Withdrawn
- 1975-03-06 CH CH288275A patent/CH616842A5/de not_active IP Right Cessation
- 1975-04-25 FR FR7513032A patent/FR2268789B1/fr not_active Expired
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3536723A (en) * | 1966-09-27 | 1970-10-27 | Menarini Soc In Accomandita Se | P - (2 - alkyloxy - benzoyl) - aminobenzoates of n - dialkylamine - alkyl and their quaternary salts |
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU569940B2 (en) * | 1984-06-21 | 1988-02-25 | Van Dyk & Company | Benzene sulfonate quaternary ammonium salts of sunscreen carboxylic acids |
| US5427774A (en) * | 1993-08-25 | 1995-06-27 | Isp Van Dyk Inc. | Heterocyclic quaternary salts of para-dialkylamino benzamide derivatives |
| US5427773A (en) * | 1993-08-25 | 1995-06-27 | Isp Van Dyk Inc. | Quaternary salts of dialkylaminobenzamides |
| US5869443A (en) * | 1994-07-26 | 1999-02-09 | The Procter & Gamble Company | Dryer-added fabric treatment article of manufacture containing antioxidant and sunscreen compounds for sun fade protection of fabrics |
| US5705474A (en) * | 1994-07-26 | 1998-01-06 | The Procter & Gamble Company | Rinse added fabric softener compositions containing sunscreens for sun-fade protection for fabrics |
| US5723435A (en) * | 1994-07-26 | 1998-03-03 | The Procter & Gamble Company | Rinse added fabric softener compositions containing antioxidants for sun-fade protection fabrics |
| US5733855A (en) * | 1994-07-26 | 1998-03-31 | The Procter & Gamble Company | Dryer-added fabric treatment article of manufacture containing antioxidant and sunscreen compounds for sun fade protection of fabrics |
| US5474691A (en) * | 1994-07-26 | 1995-12-12 | The Procter & Gamble Company | Dryer-added fabric treatment article of manufacture containing antioxidant and sunscreen compounds for sun fade protection of fabrics |
| US5543083A (en) * | 1994-07-26 | 1996-08-06 | The Procter & Gamble Company | Fatty amine derivatives of butylated hydroxy toluene for the protection of surfaces from physical and chemical degradation |
| US7396526B1 (en) | 1998-11-12 | 2008-07-08 | Johnson & Johnson Consumer Companies, Inc. | Skin care composition |
| US20040213754A1 (en) * | 2000-10-02 | 2004-10-28 | Cole Curtis A. | Method for cleansing sensitive skin using an alkanolamine |
| US20040191206A1 (en) * | 2000-10-02 | 2004-09-30 | Curtis Cole | Methods for reduction of inflammation and erythema |
| US20030202951A1 (en) * | 2000-12-21 | 2003-10-30 | Curtis Cole | Method for reducing the appearance of dark circles under the eyes |
| US6607735B2 (en) | 2000-12-21 | 2003-08-19 | Johnson & Johnson Consumer Companies, Inc. | Method for reducing the appearance of dark circles under the eyes |
| US20080063844A1 (en) * | 2001-06-29 | 2008-03-13 | Mannington Mills, Inc. | Surface coverings containing aluminum oxide |
| US20050238730A1 (en) * | 2001-11-21 | 2005-10-27 | Agnes Le Fur | Compositions comprising an ethanolamine derivative and organic metal salts |
| CN109232285A (en) * | 2018-10-16 | 2019-01-18 | 新乡学院 | A kind of synthetic method and application of the benzocainum disubstituted derivative with antibacterial activity |
Also Published As
| Publication number | Publication date |
|---|---|
| CA1064049A (en) | 1979-10-09 |
| FR2268789B1 (en) | 1979-08-17 |
| DE2509647A1 (en) | 1975-11-13 |
| GB1428648A (en) | 1976-03-17 |
| JPS50140642A (en) | 1975-11-11 |
| FR2268789A1 (en) | 1975-11-21 |
| CH616842A5 (en) | 1980-04-30 |
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