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1323-03-1

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1323-03-1 Usage

Description

Lactic Acid Tetradecyl Ester, also known as Myristyl Lactate or Tetradecyl Lactate, is a versatile compound derived from lactic acid and tetradecyl alcohol. It possesses emollient and moisturizing properties, making it suitable for various applications in the cosmetic and agricultural industries. Its light texture and good spreadability contribute to a smooth, satiny afterfeel, while its herbicidal properties make it an effective component in agricultural formulations.

Uses

Used in Cosmetic Industry:
Lactic Acid Tetradecyl Ester is used as a light emollient and moisturizer for its good spreadability and smooth, satiny afterfeel. It is particularly useful in formulations that require a non-greasy, non-comedogenic ingredient to provide hydration and improve skin texture.
Used in Agricultural Industry:
Lactic Acid Tetradecyl Ester is used as a herbicide compound with improved properties, making it an effective ingredient in agricultural formulations for controlling weed growth. Its herbicidal action helps in protecting crops and enhancing agricultural productivity.
Used in Cosmetic Compounds:
In the cosmetic industry, Lactic Acid Tetradecyl Ester is also used as a compound for compressing silicones and oils. This application helps in creating stable, easy-to-apply formulations with a pleasant texture and feel, enhancing the overall user experience.

Check Digit Verification of cas no

The CAS Registry Mumber 1323-03-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,3,2 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1323-03:
(6*1)+(5*3)+(4*2)+(3*3)+(2*0)+(1*3)=41
41 % 10 = 1
So 1323-03-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H34O3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-20-17(19)16(2)18/h16,18H,3-15H2,1-2H3

1323-03-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetradecyl Lactate

1.2 Other means of identification

Product number -
Other names Tetradecyl 2-Hydroxypropionate

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:1323-03-1 SDS

1323-03-1Downstream Products

1323-03-1Relevant articles and documents

Synthesis and Evaluation of Surface and Biological Properties of Some Lactic Acid-Based Anionic Surfactants

Sathyam Reddy, Yasa,Sujitha, Pombala,Kumar, Chityal Ganesh,Kanjilal, Sanjit,Vijayalakshmi, Penumarthy

, p. 943 - 951 (2016)

In the present study, 11 lactic acid-based anionic surfactants were synthesized and evaluated for their surface and biological activities. The synthesis involved the esterification of lactic acid with a range of fatty alcohols differing in chain length as well as in branching and unsaturation. The resultant ester was sulfonated by treatment with chlorosulfonic acid followed by salt formation with aqueous NaOH solution. The surface properties of all the synthesized surfactants were determined using surface tensiometry. Synthesized surfactants showed low critical micelle concentration (CMC) values and a decreasing trend with an increase in the alkyl chain length. Alkyl branching also led to a mild change in CMC values when compared with linear counterparts having the same number of carbon atoms, though such decreases or increases were observed to be dependent on the position and number of the branching. Some of the synthesized surfactants exhibited good antimicrobial and anti-cancer activities against the tested microbial strains and cell lines.

Ultraviolet resistant sunscreen compositions

-

, (2008/06/13)

A sunscreen composition for leaving a protective film on skin, comprising a UVB light absorbing sunscreen, a polymer vehicle, an oil-soluble solubilizer, and alkoxylated castor oil as an emulsifier. The protective film has an aggregate cohesive energy of from about 80 to about 150 calories per cc, preferably 100 to 115 calories/cc. The film is water resistant, unusually stable to UV radiation, nonirritating, and physically protective.

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