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605-84-5

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605-84-5 Usage

Chemical compound

Yes

Usage

Crosslinking agent in polymer production

Azo compound

Yes

Physical state

Reddish-brown crystalline solid

Solubility

Readily soluble in organic solvents

Melting point

High

Applications

Manufacturing of rubber and plastic products

Function

Improves mechanical strength and heat resistance

Hazardous classification

Classified as a hazardous chemical

Handling and storage

Requires careful handling and storage to avoid health and environmental risks

Check Digit Verification of cas no

The CAS Registry Mumber 605-84-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 605-84:
(5*6)+(4*0)+(3*5)+(2*8)+(1*4)=65
65 % 10 = 5
So 605-84-5 is a valid CAS Registry Number.

605-84-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name di-[1]naphthyl-diazene-N-oxide

1.2 Other means of identification

Product number -
Other names di-1-naphthalenyl-diazene,1-oxide

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:605-84-5 SDS

605-84-5Relevant articles and documents

An easy access to aromatic azo compounds under ultrasound/microwave irradiation

Cravotto, Giancarlo,Boffa, Luisa,Bia, Marco,Bonrath, Werner,Curini, Massimo,Heropoulos, Georgios A.

, p. 2605 - 2608 (2008/09/16)

Chemoselective reduction of nitroarenes to azo and azoxy compounds was easily achieved using zinc powder and ammonium chloride in DMF or DMF-water (95:5) under high intensity ultrasound (US) or microwave (MW) irradiation, separately or combined. When carried out under conventional heating the reaction required much higher temperatures and gave lower yields. The addition of a small amount of water caused a dramatic increase in the reactivity, permitting the reduction of hindered nitroarenes at the expense of selectivity. A novel reactor for combined US/MW irradiation was employed which demonstrated additional beneficial effects. Georg Thieme Verlag Stuttgart.

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