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76387-44-5

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76387-44-5 Usage

Description

(1E)-1,3-dibutyl-3-methyltriaz-1-ene is a colorless liquid chemical compound belonging to the class of triazenes, which are organic compounds containing a triazene group with a terminal double bond. This specific compound features a butyl group and a methyl group attached to the triazenic ring, and has a molecular formula of C11H22N3 with a molecular weight of 190.31 g/mol.

Uses

Used in Chemical Synthesis Processes:
(1E)-1,3-dibutyl-3-methyltriaz-1-ene is used as a chemical intermediate for various synthesis processes, contributing to the creation of different compounds and materials.
Used in Pharmaceutical Sector:
In the pharmaceutical industry, (1E)-1,3-dibutyl-3-methyltriaz-1-ene is used as a building block for the development of new drugs, potentially offering novel therapeutic agents.
Used in Agricultural Sector:
(1E)-1,3-dibutyl-3-methyltriaz-1-ene may be utilized in the agricultural sector for the synthesis of agrochemicals, such as pesticides or herbicides, to improve crop protection.
Used in Industrial Sector:
(1E)-1,3-dibutyl-3-methyltriaz-1-ene may also find applications in the industrial sector, where it could be employed in the production of various industrial chemicals or materials.
Used in Research and Development:
(1E)-1,3-dibutyl-3-methyltriaz-1-ene is used in research and development settings to explore its properties and potential applications, as further studies are needed to fully understand its capabilities and uses.

Check Digit Verification of cas no

The CAS Registry Mumber 76387-44-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,8 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76387-44:
(7*7)+(6*6)+(5*3)+(4*8)+(3*7)+(2*4)+(1*4)=165
165 % 10 = 5
So 76387-44-5 is a valid CAS Registry Number.

76387-44-5SDS

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 N-(butyldiazenyl)-N-methylbutan-1-amine

1.2 Other means of identification

Product number -
Other names 1,3-di-n-butyl-3-methyltriazene

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:76387-44-5 SDS

76387-44-5Relevant articles and documents

Acid-Catalyzed Decomposition of Trialkyltriazenes: Protected Alkyldiazonium Ions

Sieh, David H.,Michejda, Christopher J.

, p. 442 - 445 (1981)

The ecid-catalyzed decomposition of 1,3-di-n-butyl-3-methyltriazene and the synthesis and decomposition of 1,3-bis(cyclprpopylcarbinyl)-3-methyltriazene are reported.A kinetic study of the acid-catalyzed decomposition of 1,3-di-n-butyl-3-methyltriazene indicates that the reaction is subject to general acid catalysis.The rates of reaction have been studied by monitoring the disappearance of a triazene UV absorption band (263 nm).A plot of the buffer concentration vs. kobsd was a straight line, whose slope gave kcat = 1.84 *10-2 min-1M-1.A linear dependence of the log (kobsd) on pH (6.9 - 8.4) was observed, along with a solvent isotope effect (kD/kH) of 2.05.The products of the decomposition of the butyltriazene (n-butyl and sec-butyl alcohols and 1- and 2-butene) were accounted for by the intermediacy of a diazonium ion.The mechanism was corroborated by the product analysis of the decomposition of the (cyclopropylcarbinyl)triazene.The alcoholic products isolated were cyclopropylcarbinyl alcohol (48percent), cyclobutyl alcohol (48percent) and 3-buten-1-ol (4percent).This distribution is conclusive evidence that these trialkyltriazenes decompose in aqueous media to produce alkyldiazonium ions or directly to prduce carbonium ions in cases where the alkyl group is capable of stabilizing a positive charge.

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