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85652-29-5

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85652-29-5 Usage

Physical properties

Clear colorless liquid with a mild, sweet odor

Common uses

Solvent in industrial processes (e.g. production of lacquers, paints, coatings, plasticizers, rubber chemicals), raw material in the manufacturing of adhesives, sealants, cleaning and degreasing agents, intermediate in the production of other chemical compounds, fragrance industry, flavoring agent in the food industry

Safety precautions

Can be harmful if inhaled, ingested, or comes into contact with the skin or eyes

Check Digit Verification of cas no

The CAS Registry Mumber 85652-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,5 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 85652-29:
(7*8)+(6*5)+(5*6)+(4*5)+(3*2)+(2*2)+(1*9)=155
155 % 10 = 5
So 85652-29-5 is a valid CAS Registry Number.

85652-29-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(6-hydroxyhexylamino)hexan-1-ol

1.2 Other means of identification

Product number -
Other names 7-azatridecane-1,13-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:85652-29-5 SDS

85652-29-5Downstream Products

85652-29-5Relevant articles and documents

Sequential hydroaminomethylation/Pd-catalyzed hydrogenolysis as an atom efficient route to valuable primary and secondary amines

October, Jacquin,Mapolie, Selwyn F.

, (2021)

The facile synthesis of valuable primary and secondary amines is reported using a sequential procedure of hydroaminomethylation and Pd-catalyzed hydrogenolysis. The hydroaminomethylation reaction was catalyzed by a cationic Rh(I) iminopyridyl complex and the N-alkylated benzylamines were produced with high chemoselectivity, albeit as mixtures of linear and branched products. Performing the hydrogenolysis reaction using 10% Pd/C, provided access to valuable primary and secondary amines which have applications in the surfactant, pharmaceutical and polymer industries.

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