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96-15-1

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96-15-1 Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 96-15-1 differently. You can refer to the following data:
1. CLEAR COLOURLESS TO SLIGHTLY YELLOW LIQUID
2. Colorless to yellowish liquid; fishy aroma.

Aroma threshold values

High strength odor, fishy type; recommend smelling in a 0.10% solution or less.

Check Digit Verification of cas no

The CAS Registry Mumber 96-15-1 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 96-15:
(4*9)+(3*6)+(2*1)+(1*5)=61
61 % 10 = 1
So 96-15-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H13N/c1-3-5(2)4-6/h5H,3-4,6H2,1-2H3/p+1/t5-/m1/s1

96-15-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-METHYLBUTYLAMINE

1.2 Other means of identification

Product number -
Other names 2-Mehtylbutylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:96-15-1 SDS

96-15-1Relevant articles and documents

DECARBOXYLATION OF AMINO ACIDS. IV.

SUYAMA,KANAO

, p. 531 - 533 (1965)

-

One-pot reductive amination of carboxylic acids: a sustainable method for primary amine synthesis

Coeck, Robin,De Vos, Dirk E.

supporting information, p. 5105 - 5114 (2020/08/25)

The reductive amination of carboxylic acids is a very green, efficient and sustainable method for the production of (bio-based) amines. However, with current technology, this reaction requires two to three reaction steps. Here, we report the first (heterogeneous) catalytic system for the one-pot reductive amination of carboxylic acids to amines, with solely H2 and NH3 as the reactants. This reaction can be performed with relatively cheap ruthenium-tungsten bimetallic catalysts in the green and benign solvent cyclopentyl methyl ether (CPME). Selectivities of up to 99% for the primary amine could be achieved at high conversions. Additionally, the catalyst is recyclable and tolerant for common impurities such as water and cations (e.g. sodium carboxylate).

Amination of aliphatic alcohols with urea catalyzed by ruthenium complexes: effect of supporting ligands

Dindar, Sara,Nemati Kharat, Ali

, (2020/09/02)

In the present study, ruthenium-catalyzed amination of alcohols by urea as a convenient ammonia carrier in the presence of free diphosphine ligands has been described. A number of ruthenium-phosphine complexes have been studied among which, [(Cp)RuCl(dppe)] was found as an efficient catalyst for alcohol amination reaction. The crystal structures of two new half-sandwich ruthenium complexes, [(Cp)RuCl(dppe)] and [(C6H6)RuCl2(PHEt2)], were determined by X-ray crystallographic analysis. Also the effect of using different supporting phosphines, ratio of raw materials and reaction temperature on conversion and selectivity was investigated. Under optimum reaction conditions high conversion (98percent) and chemo-selectivity toward secondary amines were obtained.

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