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ALPHA-N-ETHYL-1-NAPHTHYLAMINE HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36101-15-2

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36101-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36101-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,1,0 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 36101-15:
(7*3)+(6*6)+(5*1)+(4*0)+(3*1)+(2*1)+(1*5)=72
72 % 10 = 2
So 36101-15-2 is a valid CAS Registry Number.

36101-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Ethyl-1-naphthylamine hydrochloride (α-)

1.2 Other means of identification

Product number -
Other names Ethylnaphthylaminehydrochloride

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:36101-15-2 SDS

36101-15-2Upstream product

36101-15-2Downstream Products

36101-15-2Relevant academic research and scientific papers

TRI- AND TETRA-SUBSTITUTED GUANIDINES AND THEIR USE AS EXCITATORY AMINO ACID ANTAGONISTS

-

, (2008/06/13)

Tri-and tetra-substituted guanidines which exhibit a high binding affinity to phencyclidine (PCP) receptors and, more preferably, low affinity to the brain sigma receptors. These guanidine derivatives act as non-competitive inhibitorsSTATEMENT AS TO RIGHT

Benzoindole phthalides

-

, (2008/06/13)

A chromogenic compound of normally colorless form is disclosed having the following structural formula: STR1 wherein A can be aminophenyl, indolyl, and benzoindolyl, substituted or not; B can be benzoindolyl, substituted or not; and E can be a broad family of aromatic and heterocyclic structures. The compound is eligible for use in pressure-sensitive record materials and manifold marking systems. Because of light absorption characteristics, selected compounds of this invention are especially useful where broad spectrum absorption and machine readability are important.

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