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cyclohexyl(isopropyl)methylammonium chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1007-33-6

1007-33-6 Suppliers

This product is a nationally controlled contraband or patented product, and the Lookchem platform doesn't provide relevant sales information.

1007-33-6 Usage

Chemical Properties

White Solid

Uses

Adrenergic (vasoconstrictor); decongestant (nasal).

Check Digit Verification of cas no

The CAS Registry Mumber 1007-33-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1007-33:
(6*1)+(5*0)+(4*0)+(3*7)+(2*3)+(1*3)=36
36 % 10 = 6
So 1007-33-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H21N.ClH/c1-9(2)11(3)10-7-5-4-6-8-10;/h9-10H,4-8H2,1-3H3;1H

1007-33-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexyl-N-methylpropan-2-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names Eventin hydrochloride

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:1007-33-6 SDS

1007-33-6Downstream Products

1007-33-6Relevant academic research and scientific papers

PROCESS FOR PREPARING BENZYLATED AMINES

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Page/Page column 8, (2008/06/13)

This present invention relates to a process for preparing benzylated amines by the reaction of an amine selected from methamphetamine and propylhexedrine with benzyl halide. Numerous improvements are obtained by employing the amine in molar excess with respect to benzyl halide, preferably in a molar ratio of 2 to 1. The excess amine is employed to selectively neutralize by-product acid as the amine salt. The amine salt is then separated from the reaction mixture and basified to reclaim starting amine for recycle to the process.