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31367-46-1

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31367-46-1 Usage

General Description

3-Methyl-2-heptanol is a chemical compound that belongs to the family of alcohols. Also known as isobutyl amyl carbinol, it is a colorless liquid with a slight odor. It is commonly used as a solvent in the manufacture of perfumes, flavors, and other chemical products. It is also used as a chemical intermediate in the production of plasticizers, lubricants, and detergents. Additionally, 3-methyl-2-heptanol is used in the synthesis of pharmaceuticals and agrochemicals. Its chemical properties make it useful in a wide range of industries, although it should be handled with care due to its flammability and potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 31367-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,3,6 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31367-46:
(7*3)+(6*1)+(5*3)+(4*6)+(3*7)+(2*4)+(1*6)=101
101 % 10 = 1
So 31367-46-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H18O/c1-4-5-6-7(2)8(3)9/h7-9H,4-6H2,1-3H3

31367-46-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylheptan-2-ol

1.2 Other means of identification

Product number -
Other names 3-methyl-heptan-2-ol

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:31367-46-1 SDS

31367-46-1Relevant articles and documents

Stereochemistry of Aliphatic Carbocations, 13. Protonated Cyclopropanes as Intermediates in 1,2-Alkyl Shifts

Kirmse, Wolfgang,Loosen, Karin,Prolingheuer, Ernst-Christoph

, p. 129 - 141 (2007/10/02)

The nitrous acid deamination of 2-ethyl-1-methylbutylamine (10), 1,2-diethylbutylamine (35), and 2-ethyl-1-methylpentylamine (43) has been studied with respect to 1,2-alkyl shifts.Optically active and deuterated amines were employed whenever possible.The structure, configuration, and deuterium distribution of various products (e. g. 16 from 10, 40 and 48 from 35, 56 from 43) are most reasonably explained in terms of alkyl-bridged intermediates (corner-protonated cyclopropanes) which isomerize via proton shifts from corner to corner.The alternative interconversion of open ions via 1,3-H shifts is incompatible with our experimental results.

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