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4253-64-9

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4253-64-9 Usage

Chemical origin

Derived from stearic acid, a saturated fatty acid found in animal and vegetable fats.

Classification

Ester, formed from the reaction of stearic acid with ethanolamine.

Common uses

Emollient and emulsifier in cosmetics and personal care products.

Skin benefits

Softens and smooths the skin, making it a popular ingredient in moisturizers, lotions, and creams.

Additional properties

Antimicrobial and anti-inflammatory properties.

Role in skincare

Enhances the texture and efficacy of various skincare products.

Check Digit Verification of cas no

The CAS Registry Mumber 4253-64-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,5 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4253-64:
(6*4)+(5*2)+(4*5)+(3*3)+(2*6)+(1*4)=79
79 % 10 = 9
So 4253-64-9 is a valid CAS Registry Number.
InChI:InChI=1/C21H40O4/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-20(22)25-19(2)21(23)24/h19H,3-18H2,1-2H3,(H,23,24)

4253-64-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name O-stearoyl lactic acid

1.2 Other means of identification

Product number -
Other names Octadecanoic acid 1-carboxy-ethyl 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:4253-64-9 SDS

4253-64-9Downstream Products

4253-64-9Relevant articles and documents

EXTRAHEPATIC DELIVERY

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, (2021/05/15)

One aspect of the present invention relates to a compound comprising an antisense strand which is complementary to a target gene; a sense strand which is complementary to said antisense strand; and one or more lipophilic monomers, containing one or more lipophilic moieties, conjugated to one or more positions on at least one strand, optionally via a linker or carrier. Another aspect of the invention relates to a method of gene silencing, comprising administering to a cell or a subject in need thereof a therapeutically effective amount of the lipophilic monomer-conjugated compound.

ESTER FORMATION OF FATTY ACID AND HYDROXYCARBOXYLIC AID

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Page/Page column 8, (2014/01/09)

The present invention relates to a process for the transesterification of a fatty acid ester of a lower alcohol and a salt of hydroxycarboxylic acid without making use of organic solvents. The process can also be carried out without added anionic surface active agents.

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