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1,6-Octanediol is a colorless, viscous liquid with the chemical formula C8H18O2. It is an organic compound that belongs to the class of diols, characterized by the presence of two hydroxyl (-OH) groups. This specific diol has its hydroxyl groups located at the first and sixth carbon atoms of an octane chain, which consists of eight carbon atoms in total. 1,6-Octanediol is used in various applications, including the production of polyurethanes, as a solvent, and in the synthesis of other chemicals. It is also known for its ability to act as a humectant, helping to retain moisture in products. The compound has a molecular weight of 146.23 g/mol and is insoluble in water but soluble in organic solvents. It is important to handle 1,6-Octanediol with care due to its potential irritant properties and to follow proper safety procedures when working with it.

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 academic research and scientific papers

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

Ytterbium triflate mediated selective deprotection of acetates

Sharma,Ilangovan

, p. 1963 - 1965 (2007/10/03)

Ytterbium triflate mediated selective deprotection of acetates in isopropyl alcohol at reflux temperature is reported. Unlike hafnium triflate, under the present reaction conditions aryl acetates also undergo deacetylation instead of Fries migration.

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