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10108-22-2

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10108-22-2 Usage

Description

3-Hydroxypropyl laurate is a chemical compound derived from the esterification of lauric acid, a saturated fatty acid, with 1,2,3-propanetriol. It is known for its emollient, thickening, and moisturizing properties, making it a valuable ingredient in personal care and cosmetic products.

Uses

Used in Personal Care Products:
3-Hydroxypropyl laurate is used as an emollient and thickening agent for its ability to soften and smooth the skin and hair, enhancing the texture and feel of lotions, creams, and hair care products.
Used in Cosmetic Formulations:
3-Hydroxypropyl laurate is used as a moisturizing agent to improve the hydration and overall quality of cosmetic products, ensuring a pleasant application and long-lasting effects on the skin and hair.
Used in the Cosmetic Industry:
3-Hydroxypropyl laurate is widely utilized in the cosmetic industry for its safe and effective properties, contributing to the development of high-quality skincare and haircare products that cater to various consumer needs.

Check Digit Verification of cas no

The CAS Registry Mumber 10108-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,0 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10108-22:
(7*1)+(6*0)+(5*1)+(4*0)+(3*8)+(2*2)+(1*2)=42
42 % 10 = 2
So 10108-22-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H30O3/c1-2-3-4-5-6-7-8-9-10-12-15(17)18-14-11-13-16/h16H,2-14H2,1H3

10108-22-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxypropyl dodecanoate

1.2 Other means of identification

Product number -
Other names lauric acid-(3-hydroxy-propyl ester)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10108-22-2 SDS

10108-22-2Downstream Products

10108-22-2Relevant articles and documents

Contiguous versus segmented hydrophobicity in micellar systems

Menger, Fredric M.,Galloway, Ashley L.

, p. 15883 - 15889 (2004)

This paper addresses a question not yet posed systematically in surfactant chemistry: How do the colloidal properties of surfactants respond to insertion of non-hydrocarbon functionalities (i.e., ester groups) within chains that are normally entirely hydrocarbon? In answering this question, two classes of such chain-modified surfactants were discovered. One class forms only small aggregates with noncooperative self-assembly, low foaming, high areas of occupancy at the air/water interface, and weak solid-adsorption and solubilization properties. The other class is much more normal with regard to these properties and, in fact, can even exceed conventional surfactants in mesitylene solubilization. Differences between the two categories of chain-modified surfactants originate from the degree of segmentation of the hydrocarbon and, in particular, upon the location of the longest segment. Segmented hydrophobicity, having in principle a "hydrophobic potential" similar to that of a contiguous hydrophobicity of equal length, can induce aggregation but, concurrently, alters the mode of assembly into films and micelles.

Facile and efficient synthesis of hydroxyalkyl esters from cyclic acetals through aerobic photo-oxidation using anthraquinone-2-carboxylic acid

Yamaguchi, Tomoaki,Kudo, Yasuhisa,Hirashima, Shin-ichi,Yamaguchi, Eiji,Tada, Norihiro,Miura, Tsuyoshi,Itoh, Akichika

, p. 1973 - 1975 (2015/03/18)

Abstract A convenient metal-free oxidation protocol of various cyclic acetals with molecular oxygen and anthraquinone-2-carboxylic acid under visible light irradiation by a fluorescent lamp afforded their corresponding hydroxyalkyl esters.

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