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4066-76-6

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4066-76-6 Usage

Physical state

Colorless, highly viscous liquid

Odor

Mild, pleasant

Chemical intermediate

Used in the production of pharmaceuticals, fragrances, and other chemicals

Solvent

Utilized as a solvent in various chemical processes

Humectant

Used in personal care products and cosmetics to retain moisture

Component in manufacturing

Polyesters and polyurethane resins

Antimicrobial properties

Suitable for use in anti-bacterial and anti-fungal products

Versatility

Wide range of industrial and commercial applications

Check Digit Verification of cas no

The CAS Registry Mumber 4066-76-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,6 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4066-76:
(6*4)+(5*0)+(4*6)+(3*6)+(2*7)+(1*6)=86
86 % 10 = 6
So 4066-76-6 is a valid CAS Registry Number.

4066-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-octandiol

1.2 Other means of identification

Product number -
Other names Octan-1,6-diol

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:4066-76-6 SDS

4066-76-6Downstream Products

4066-76-6Relevant articles and documents

Intramolecular C-H bond activation through a flexible ester linkage

Shaffer, Christopher J.,Schroeder, Detlef,Guetz, Christoph,Luetzen, Arne

, p. 8097 - 8100 (2012)

Replacing the director: A bipyridinyl ligand with an aliphatic side chain determines the regioselectivity of copper-catalyzed C-H oxidation by intramolecular effects. Because the aliphatic chain is attached through an ester linkage, the catalytic cycle can in principle be closed by transesterification. Ion-mobility mass spectrometry and isotopic labeling provide mechanistic insight not available from direct mass spectrometry experiments. Copyright

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