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Octyl lactate is a colorless, oily liquid that is widely used as a solvent, emollient, and skin conditioning agent in the cosmetics and personal care industry. It is derived from the esterification of octyl alcohol and lactic acid, which gives it excellent solubility properties and compatibility with various cosmetic ingredients. Octyl lactate is known for its ability to provide a smooth, non-greasy feel to formulations, making it a popular choice for lotions, creams, and other skincare products. It is also valued for its moisturizing and soothing effects on the skin, as well as its ability to enhance the stability and performance of other ingredients in a formulation. Overall, octyl lactate is a versatile and beneficial component in many personal care products, offering both functional and sensory benefits to consumers.

5464-71-1

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5464-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5464-71-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5464-71:
(6*5)+(5*4)+(4*6)+(3*4)+(2*7)+(1*1)=101
101 % 10 = 1
So 5464-71-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H22O3/c1-3-4-5-6-7-8-9-14-11(13)10(2)12/h10,12H,3-9H2,1-2H3

5464-71-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name n-octyl lactate

1.2 Other means of identification

Product number -
Other names octyl lactylate

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:5464-71-1 SDS

5464-71-1Relevant academic research and scientific papers

The chiral pool as valuable natural source: New chiral mesogens made from lactic acid

Brombach,Neudoerfl,Blunk

scheme or table, p. 62 - 74 (2012/01/06)

Twenty new enantiopure chiral materials have been synthesized, showing liquid crystalline phases of smectic (SmA*), twisted grain boundary (TGB) and cholesteric (N*) type. The central ester-linkage as well as the length of the attached alkyl-chains were varied in a systematic way and the effects of these structural changes on the liquid crystalline properties have been studied. The liquid crystalline phases were characterized by means of differential scanning calorimetry, polarisation microscopy as well as small angle X-ray diffraction (SAXS). Copyright Taylor & Francis Group, LLC.

SmI2-INDUCED HIGHLY REGIOSELECTIVE REDUCTION OF α,β-EPOXY ESTERS AND γ,δ-EPOXY-α,β-UNSATURATED ESTERS. AN EFFICIENT ROUTE TO OPTICALLY ACTIVE β-HYDROXY AND δ-HYDROXY ESTERS

Otsubo, Kenji,Inanaga, Junji,Yamaguchi, Masaru

, p. 4437 - 4440 (2007/10/02)

α,β-Epoxy esters were rapidly reduced at room temperature to yield β-hydroxy esters with retention of the configurations at the β-carbon atoms by using SmI2-THF-HMPA system in the presence of N,N-dimethylaminoethanol (DMAE).The conditions were successfully applied to the synthesis of vinylogous δ-hydroxy esters.

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