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1-Propanamine, N-(1,1-dimethylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22675-81-6

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22675-81-6 Usage

Physical state

Clear, colorless liquid

Odor

Strong, ammonia-like

Uses

Production of rubber chemicals, pharmaceuticals, solvent in manufacturing of pesticides and herbicides, stabilizer for dyes and resins, production of fuel additives

Hazards

Flammable and hazardous substance, requires careful handling and storage.

Check Digit Verification of cas no

The CAS Registry Mumber 22675-81-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,6,7 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22675-81:
(7*2)+(6*2)+(5*6)+(4*7)+(3*5)+(2*8)+(1*1)=116
116 % 10 = 6
So 22675-81-6 is a valid CAS Registry Number.

22675-81-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-N-propylpropan-2-amine

1.2 Other means of identification

Product number -
Other names tert-butyl-n-propylamine

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:22675-81-6 SDS

22675-81-6Relevant academic research and scientific papers

Hindered ureas as masked isocyanates: Facile carbamoylation of nucleophiles under neutral conditions

Hutchby, Marc,Houlden, Chris E.,Gair Ford,Tyler, Simon N. G.,Gagne, Michel R.,Lloyd-Jones, Guy C.,Booker-Milburn, Kevin I.

supporting information; experimental part, p. 8721 - 8724 (2010/01/16)

Bigger is better: Sterically hindered dialkyl ureas undergo nucleophilic substitution at dramatically faster rates than their less hindered counterparts (see scheme). Steric decompression upon the formation of an intermediate isocyanate can explain this c

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