58761-87-8

Usage

Uses

Used in Personal Care Industry:
Sodium lauryl sulfoacetate is used as a foaming and cleansing agent in personal care products such as shampoos, body washes, and facial cleansers. It is favored for its mildness and reduced skin irritation compared to other cleansing agents, making it suitable for sensitive skin types.
Used in Bath Product Industry:
In the bath product industry, sodium lauryl sulfoacetate is used to create a luxurious and foamy lather in products like bath bombs. Its ability to produce a rich foam enhances the sensory experience of bathing, contributing to the product's appeal and effectiveness.
Used as an Environmentally Friendly Alternative:
Sodium lauryl sulfoacetate is used as a milder and more environmentally friendly alternative to sodium lauryl sulfate. Its biodegradable nature makes it a preferred choice for manufacturers aiming to reduce the ecological impact of their products while maintaining high performance in terms of cleansing and foaming capabilities.

InChI:InChI=1/C21H23NO5S/c1-3-4-5-6-7-13-10-15(28(2,22)26)12-17-19(23)16-11-14(21(24)25)8-9-18(16)27-20(13)17/h8-12,22H,3-7H2,1-2H3,(H,24,25)

Upstream product

• 58762-17-7 methyl 7-methylsulfinyl-5-(n-hexyl)-xanthone-2-carboxylate 
• 58761-98-1 methyl 7-methylthio-5-(n-hexyl)-xanthone-2-carboxylate 
• 58761-97-0 5-n-hexyl-7-(methylthio)-xanthone-2-carboxylic acid 
• 58761-96-9 4-[4'-methylthio-2'-(n-hexyl)-phenoxy]-isophthalic acid 
• 58761-93-6 4-methylthio-2-(n-hexyl)-phenol 
• 28730-78-1 4-bromo-1,3-benzenedicarboxylic acid dimethyl ester 
• 58762-16-6 methyl 7-(S-methylsulfonimidoyl)-5-(n-hexyl)-xanthone-2-carboxylate 

Relevant academic research and scientific papers

Process for preparing 5-alkyl-7-(S-alkyl-sulfonimidoyl)-xanthone-2-carboxylic acids

A novel process for the preparation of xanthane-2-carboxylic acids of the formula STR1 wherein R is selected from the group consisting of hydrogen and alkyl of 1 to 9 carbon atoms and R1 is alkyl of 1 to 5 carbon atoms which possess an antialle

Xanthone-2-carboxylic acid compounds

Novel xanthone-2-carboxylic acid compounds of the formula STR1 wherein A is selected from the group consisting of --COOR', a 1H-tetrazol-5-yl and a 1H-tetrazolylcarbamoyl, R' is selected from the group consisting of hydrogen, alkyl of 1 to 5 carbon atoms and cation of a non-toxic, pharmaceutically acceptable organic or inorganic base, R is selected from the group consisting of hydrogen, alkyl of 1 to 9 carbon atoms, alkoxy of 1 to 9 carbon atoms and alkoxy alkoxy of 2 to 9 carbon atoms and X is selected from the group consisting of STR2 AND STR3 WHEREIN R1 is alkyl of 1 to 5 carbon atoms, R2 is selected from the group consisting of hydrogen, acyl of an aliphatic acid of 1 to 5 carbon atoms, aroyl of 7 to 8 carbon atoms, araliphatic acyl with 1 to 5 carbon atoms in the aliphatic portion and 6 or 7 carbon atoms in the aryl portion, aralkyl of 7 to 8 carbon atoms, arylsulfonyl, a carbamoyl, a carboxyalkyl of 1 to 5 carbon atoms, --CO--(CH2)n -- Het where n is 1, 2 or 3 and Het is a N-attached nitrogen heterocyclic which may contain an additional heteroatom and STR4 AND Alk is alkyl of 1 to 5 carbon atoms and R3 is arylsulfonyl which possess anti-allergic properties and their preparation.