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42008-54-8

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42008-54-8 Usage

Type of compound

chemical compound

Derivative of

thiourea

Common use

corrosion inhibitor for metal surfaces in industrial and commercial applications

Mechanism of action

forms stable complexes with various metal ions, inhibiting corrosion by creating a protective film on the metal surface

Additional use

chemical intermediate in the synthesis of pharmaceuticals and agricultural chemicals

Physical form

white, crystalline solid

Solubility

readily soluble in water

Toxicity

relatively non-toxic in its pure form, but should be handled with care and proper safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 42008-54-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,0 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42008-54:
(7*4)+(6*2)+(5*0)+(4*0)+(3*8)+(2*5)+(1*4)=78
78 % 10 = 8
So 42008-54-8 is a valid CAS Registry Number.

42008-54-8SDS

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 hydroxythiourea

1.2 Other means of identification

Product number -
Other names Thiourea,hydroxy

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:42008-54-8 SDS

42008-54-8Downstream Products

42008-54-8Relevant articles and documents

N-Hydroxythiosemicarbazones: Synthesis and in vitro antitubercular activity

Sriram, Dharmarajan,Yogeeswari, Perumal,Dhakla, Prathiba,Senthilkumar, Palaniappan,Banerjee, Debjani

, p. 1888 - 1891 (2007/10/03)

N-Hydroxythiosemicarbazide was prepared by two methods starting from 2,4-dimethoxy benzyl amine and hydroxylamine hydrochloride, which in turn was reacted with various aldehydes and ketones to obtain the titled compounds. Eighteen compounds were tested fo

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