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64037-35-0

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64037-35-0 Usage

Type of Compound

Quaternary ammonium salt

Uses

Local anesthetic and antipruritic in topical formulations

Mechanism of Action

Blocks transmission of pain signals and provides relief from itching and minor skin irritations

Charge

Permanent positive charge

Binding

Effectively binds to the negatively charged surface of the skin

Common Applications

Relief from minor burns, insect bites, and other skin irritations in over-the-counter products

Importance

Important ingredient in topical medications for the treatment of various skin conditions

Check Digit Verification of cas no

The CAS Registry Mumber 64037-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,3 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64037-35:
(7*6)+(6*4)+(5*0)+(4*3)+(3*7)+(2*3)+(1*5)=110
110 % 10 = 0
So 64037-35-0 is a valid CAS Registry Number.

64037-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1-phenylpentan-1-ol,hydrochloride

1.2 Other means of identification

Product number -
Other names Dioxethedrin HCl

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:64037-35-0 SDS

64037-35-0Relevant articles and documents

NON-CATALYTIC REDUCTION OF Α-OXIMINOKETONES AND Α-OXIMINOALCOHOLS TO ERYTHRO-2-AMINO-1-ARYLALKAN-1-OLS

Oppong-Boachie, Francis Kwabena

, p. 293 - 298 (2007/10/02)

A non-catalytic reduction of α-oximinoketones 1 and α-oximinoalcohols 2 to erythro-2-amino-1-arylalkan-1-ols 3 with lithium aluminium hydride is reported.The erythro-2-amino-1-arylalkan-1-ols are isolated as their hydrochlorides 5 and characterised as the erythro isomers by benzoylation.

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