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N,N,2,3,3-Pentamethylbutan-1-amine is an organic compound with the chemical formula C9H21N. It is a colorless liquid with a strong amine odor and is soluble in water. N,N,2,3,3-pentamethylbutan-1-amine is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in the production of rubber chemicals and as a catalyst in certain chemical reactions. Due to its amine functional group, it can form salts with acids and participate in various chemical reactions, making it a versatile building block in the chemical industry.

3733-36-6

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3733-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3733-36-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,3 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3733-36:
(6*3)+(5*7)+(4*3)+(3*3)+(2*3)+(1*6)=86
86 % 10 = 6
So 3733-36-6 is a valid CAS Registry Number.

3733-36-6SDS

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 N,N,2,3,3-pentamethyl-2-Butanamine

1.2 Other means of identification

Product number -
Other names -

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:3733-36-6 SDS

3733-36-6Downstream Products

3733-36-6Relevant academic research and scientific papers

Thermolysis, Photolysis, and Acid Catalysis of an α-(Dimethylamino)azoalkane. Amino Stabilization of a Carbon Radical Center

Engel, Paul S.,Wu, Wen-Xue

, p. 2720 - 2725 (2007/10/02)

The unsymmetrical azoalkane 2-(tert-butylazo)-2-(dimethylamino)propane (7) has been synthesized cleanly by nucleophilic displacement of chloride from the corresponding α-chloroazoalkane 5 with dimethylamine.Thermolysis of 7 in hydrocarbon solvents affords typical radical-derived products and exhibits activation parameters ΔH(excit.) = 26.6 +/- 0.4 kcal/mol and ΔS(excit.) = -6.6 +/- 1.1 eu.Since the thermolysis rate of 7 is 104 faster than that of 1,2-di-tert-butyldiazene, the large stabilization of α-amino radicals is supported.Unusual products were obtained in acetonitrile, suggesting reduction of the azo linkage by 2-(dimethylamino)-2-propyl radicals and cleavage of the resulting hydrazyl radicals.In protic solvents, 7 undergoes acid catalyzed decomposition via tert-butyldiazene as a postulated intermediate.

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