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1,3,5-Trimethylpiperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27644-32-2

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27644-32-2 Usage

Type of compound

Cyclic tertiary amine

Common uses

Building block in the synthesis of pharmaceuticals
Building block in the synthesis of agrochemicals
Building block in the synthesis of other fine chemicals

Potential applications

Corrosion inhibitor
Stabilizer in vinyl polymers
Precursor for the production of chiral catalysts

Utilization in manufacturing

Rubber chemicals
Surfactants

Significance in the chemical industry

Versatile properties and wide range of applications

Check Digit Verification of cas no

The CAS Registry Mumber 27644-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,4 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 27644-32:
(7*2)+(6*7)+(5*6)+(4*4)+(3*4)+(2*3)+(1*2)=122
122 % 10 = 2
So 27644-32-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H17N/c1-7-4-8(2)6-9(3)5-7/h7-8H,4-6H2,1-3H3

27644-32-2SDS

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 1,3,5-trimethylpiperidine

1.2 Other means of identification

Product number -
Other names 1,3,5-trimethyl-piperidine

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:27644-32-2 SDS

27644-32-2Downstream Products

27644-32-2Relevant academic research and scientific papers

HYDROGENATION PROCESS

-

Page/Page column 27-28, (2020/01/24)

A process for the production of heterocyclic quaternary ammonium salts or hydroxides is disclosed. The process comprises a continuous hydrogenation step, in which an unsaturated heterocyclic amine is reacted with hydrogen to form a saturated heterocyclic amine; a first continuous N-alkylation step, in which the saturated heterocyclic amine is alkylated to produce an intermediate saturated heterocyclic amine having an increased degree of substitution compared to the saturated heterocyclic amine; and one or more further N-alkylation steps in which the intermediate saturated heterocyclic amine is N-alkylated to the heterocyclic quaternary ammonium salt or hydroxide. A process of producing a saturated heterocyclic amineis also disclosed. The process comprises reacting an unsaturated heterocyclic amine with hydrogen in a vapour phase reaction at a pressure of not more than 70 bar and a temperature in the range of from 150°C to 350°C. A process of N-alkylating a saturated heterocyclic amine is also disclosed. The process comprises N-alkylating the saturated heterocyclic amine in a vapour phase reaction at a temperature of at least 2°C.

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