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Substantive water-soluble bis-quaternary salts of cinnamidoalkylamines

a technology of cinnamidoalkylamine and bis-quaternary salt, which is applied in the direction of biocide, plant growth regulator, detergent composition, etc., can solve the problems of skin damage, brittleness, and rough human hair, and achieves rough human hair, brittleness, and difficulty in combing

Inactive Publication Date: 2002-05-30
GALAXY SURFACTANTS
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The harmful effects of solar UV-radiation on skin are well known.
Continuous exposure to sunrays makes human hair color and makes human hair rough, brittle and difficult to comb.
UV rays are reported to damage the proteins of cuticles.
Prolonged irradiation results in diminished tensile strength due to breaking of disulphide bonds in keratin.
In addition, UV light is also known to fade garments.
However, all these molecules suffered from a major disadvantage of lack of substantivity.
However, they are slightly tacky, hygroscopic solids and difficult to handle and hence it is convenient to market or use these products as concentrated solutions.

Method used

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  • Substantive water-soluble bis-quaternary salts of cinnamidoalkylamines
  • Substantive water-soluble bis-quaternary salts of cinnamidoalkylamines
  • Substantive water-soluble bis-quaternary salts of cinnamidoalkylamines

Examples

Experimental program
Comparison scheme
Effect test

example i

Process for Preparation of .beta.,.beta.'-di(p-methoxy cinnamidopropyldimethylammonium chloride) ethyl ether from ethyl p-methoxy cinnamate

[0075] The compound of Formula I wherein R.sub.1=OCH.sub.3, R.sub.2=H, R.sub.3,R.sub.4=CH.sub.3, n=3, m=1, X=Cl.

[0076] p-Methoxy cinnamidopropyldimethylamine was synthesised according to procedure described below.

[0077] a) Preparation of p-methoxy cinnamidopropyldimethylamine:

[0078] Ethyl p-methoxy cinnamate (206.0 g, 1.0 mole), N,N-dimethylpropylamine (306.0 g, 3.0 mole) and sodium methoxide (2.0 g) were charged in a pressure reactor. The air inside the reactor was flushed out by purging of nitrogen. The reaction mixture was then stirred at 180.degree. C. (this generated pressure of 18 kg / cm.sup.2) for 36 hours. The progress of reaction was monitored by disappearance of ethyl p-methoxy cinnamate on chromatography (TLC and HPLC). The TLC was performed on aluminium coated silica gel plates (Merck -60-F-254) and viewed with a UV lamp at 254 nm. HPL...

example ii

Process for Preparation of .beta.,.beta.'-di(p-methoxy cinnamidopropyldimethylammonium chloride) ethyl ether from p-methoxy cinnamoyl chloride

[0085] a) Preparation of p-methoxy cinnamoyl chloride:

[0086] To a stirred suspension of p-methoxy cinnamic acid (178.0 g, 1.0 mole) in dichloromethane (500 ml), thionyl chloride (238.0 g, 2.0 moles) was added slowly and the reaction mass was heated at 45.degree. C. for 3 hours. The excess of thionyl chloride was removed under vacuum and the p-methoxy cinnamoyl chloride was distilled (145.degree. C. / 0.2 mm) in 85% yield as colorless solid with m. p. 50.degree. C. (Literature m.p. 50.degree. C., Dictionary of Organic Compounds, Chapmann and Hall, 1994).

[0087] b) Preparation of p-methoxy cinnamidopropyldimethylamine:

[0088] To a stirred solution of N,N-dimethylpropyldiamine (102.0 g, 1.0 mole) in dichloromethane (500 ml), solution of p-methoxy cinnamoyl chloride (196.0 g, 1.0 mole) in dichloromethane from step (a) was slowly added and the reaction...

example iii

Preparation of Transparent Shampoo

[0094] A shampoo composition containing .beta.,.beta.'-di(p-methoxy cinnamidopropyldimethylammonium chloride) ethyl ether of Example I was prepared in accordance with the optimum formulation given below. Acceptable formula variations for the preparation of such shampoo are also illustrated.

1 Range Preferred Optimum Ingredient % (w / w) % (w / w) % (w / w) SLES-2 (30%) 40-60 45-60 50.00 CAPB (30%) 1-10 2-10 8.00 .beta.,.beta.'-di(p-methoxy cinnamidopropyl 0.5-10 2-5 2.00 dimethylammonium chloride) ethyl ether Galsilk 3-10 4-6 5.00 Chelating agents / sodium chloride / Quantity sufficient preservatives / colour and fragrances Deionised water Quantity sufficient to make 100%

[0095] A clear shampoo was formulated using .beta.,.beta.'-di(p-methoxy cinnamidopropyldimethylammonium chloride) ethyl ether prepared as in Example I. The other active ingredients, SLES-2, Sodium lauryl ether sulphate, an anionic surfactant, 30% aqueous solution, CAPB, Cocoamidopropyl betaine,...

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Abstract

Substantive UV-absorbing water-soluble quaternary salts of cinnamidoalkylamine of formula I. Hair, skin and fabric care compositions containing the compounds of formula I. wherein R1 represents up to four substituents, same or different, selected from H, halo, -OH, -NH2, -NO2, -OCH3, -N(CH3)2, alkyl groups containing up to 6 carbon atoms, alkoxy groups containing up to 6 carbon atoms, alkylamino or N,N-dialkylamino groups containing up to 6 carbon atoms; R2 is selected from hydrogen, alkyl group containing up to 6 carbon atoms; R3 and R4 are independently selected from benzyl, alkyl group containing up to 6 carbon atoms; n is an integer from 1 to 6; m is an integer from 1 to 10; X- is a counter anion of quaternary centers selected from halides including chloride, bromide, iodide and methane sulphonate and its derivatives such as trifluoro methane sulphonate, benzene sulphonates including its p-bromo, nitro and methyl derivative.

Description

[0001] The invention relates to substantive water-soluble bis-quaternary salts of cinnamidoalkylamines. More particularly, the invention relates to novel, cationic, non-hydrolysable, non-irritating UV-absorbing bis-quaternary salts of cinnamidoalkylamines which are substantive to fabric, skin and hair. The invention also relates to a process of manufacture of the said compounds and further to their use in hair, skin and fabric care formulations.BACKGROUND AND PRIOR ART[0002] The harmful effects of solar UV-radiation on skin are well known. The UV-B (290-320 nm) portion of solar spectrum is largely responsible for erythema (sunburn) and cancer. [M. M. Rieger, Cosmet. Toiletries, 102 (3), 91, (1987); L. Taylor, Skin Cancer Foundation J., 4, (90) (1986)].[0003] Similarly, photodegradative effect of UV-radiation on human hair is well documented. Continuous exposure to sunrays makes human hair color and makes human hair rough, brittle and difficult to comb. UV rays are reported to damage...

Claims

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Application Information

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IPC IPC(8): A61K8/41A61Q5/02A61Q5/12A61Q17/04C07C233/40C11D3/28
CPCA61K8/416A61Q5/02C11D3/28A61Q17/04C07C233/40A61Q5/12
Inventor KOSHTI, NIRMAL MADHUKARJAWALE, ARUN HARCHANDRAPARAB, BHARAT BHIKAJINAIK, SHUBHANGI DATTARAMMOGHE, MANASI DATTATRAYAJADHAV, TANAJI SHAMRAONASHTE, SUBHASH SHIVLING
Owner GALAXY SURFACTANTS