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63905-16-8

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63905-16-8 Usage

Molecular Structure

A propanediol molecule with a phenyl group attached to the third carbon atom, and an acetyl group attached to the oxygens of the phenyl group.

Common Uses

Widely used in the manufacturing of cosmetics, pharmaceuticals, and industrial fluids.

Properties

Known for its moisturizing and solvent properties, making it ideal for use in lotions, creams, and serums.

Industrial Applications

Potential applications in the development of new drugs and pharmaceutical formulations due to its solvency and stability.

Versatility

A versatile and useful chemical with a variety of industrial and commercial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 63905-16-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,9,0 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63905-16:
(7*6)+(6*3)+(5*9)+(4*0)+(3*5)+(2*1)+(1*6)=128
128 % 10 = 8
So 63905-16-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O4/c1-8(13)9-2-4-11(5-3-9)15-7-10(14)6-12/h2-5,10,12,14H,6-7H2,1H3

63905-16-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(p-acetylphenoxy)-1,2-Propanediol

1.2 Other means of identification

Product number -
Other names -

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:63905-16-8 SDS

63905-16-8Relevant articles and documents

A novel and efficient biomimetic hydrolysis of oxiranes to 1,2-diols catalysed by β-cyclodextrin in water under neutral conditions

Reddy, M. Anjun,Reddy, L. Rajender,Bhanumathi, N.,Rao, K. Rama

, p. 537 - 540 (2007/10/03)

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Syntheses and studies of metaphase-arresting pyrimidinones.

Benneche,Keilen,Hagelin,Oftebro,Undheim

, p. 177 - 185 (2007/10/02)

Methods are described for the syntheses of chloromethyl hydroxyalkylphenyl and benzyl ethers, and for the synthesis of bromomethyl phenyl ketone analogs. The hydroxy groups were protected as acetates. The halogenomethyl derivatives have been used for N-al

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