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90422-09-6

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90422-09-6 Usage

Chemical compound

Yes

Industrial use

Intermediate and additive

Applications

Production of pharmaceuticals
Rubber chemicals
Agrochemicals

Functions

Corrosion inhibitor
Stabilizer in industrial processes
Reagent in organic synthesis
Solvent for extracting metal ions

Chelating properties

Useful in water treatment and metal processing applications

Acute toxicity

Low

Precautions

Prevent exposure through inhalation, ingestion, or skin contact

Handling and storage

Well-ventilated area and proper protective equipment

Check Digit Verification of cas no

The CAS Registry Mumber 90422-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,2 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90422-09:
(7*9)+(6*0)+(5*4)+(4*2)+(3*2)+(2*0)+(1*9)=106
106 % 10 = 6
So 90422-09-6 is a valid CAS Registry Number.

90422-09-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-hexylhydroxylamine

1.2 Other means of identification

Product number -
Other names 1-Hexanamine,N-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:90422-09-6 SDS

90422-09-6Upstream product

90422-09-6Relevant articles and documents

Selective synthesis of N-Alkyl hydroxylamines by hydrogenation of nitroalkanes using supported palladium catalysts

Takenaka, Yasumasa,Kiyosu, Takahiro,Choi, Jun-Chul,Sakakura, Toshiyasu,Yasuda, Hiroyuki

, p. 1166 - 1168 (2010)

The selective hydrogenation of nitroalkanes to the corresponding N-alkyl hydroxylamines is achieved at room temperature with excellent yields (up to 98 %), by using common supported palladium catalysts. The reaction temperature is key to the highly selective formation of the hydroxylamines, which proceeds smoothly in a H2 atmosphere without additives. The catalyst can be recycled up to five times.

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