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1-Triazene, 1,3-bis[4-(phenylazo)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18830-47-2

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18830-47-2 Usage

Usage

Commonly used as a dye in the textile and paper industry

Class

Triazene dyes

Known for

Vibrant and long-lasting colors

Characterized by

Two azo groups and phenyl rings

Contributes to

Intense coloration properties

Potential risks

Health and environmental risks

Reasons for caution

Possible toxicity and persistence in the environment

Check Digit Verification of cas no

The CAS Registry Mumber 18830-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,3 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18830-47:
(7*1)+(6*8)+(5*8)+(4*3)+(3*0)+(2*4)+(1*7)=122
122 % 10 = 2
So 18830-47-2 is a valid CAS Registry Number.

18830-47-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenyldiazenyl-N-[(4-phenyldiazenylphenyl)diazenyl]aniline

1.2 Other means of identification

Product number -
Other names -

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:18830-47-2 SDS

18830-47-2Upstream product

18830-47-2Downstream Products

18830-47-2Relevant academic research and scientific papers

ACID-BASE CHARACTERISTICS OF PHENYLAZOBENZENEDIAZONIUM ION

Mileiko, V. E.,Bagal, I. L.,El'tsov, A. V.

, p. 322 - 331 (2007/10/02)

The products from the reaction of phenylazobenzenediazonium ion with aqueous alkali were studied by preparative methods with TLC and electronic and IR spectroscopy.The acidity constants of the diazonium ion and the diazohydroxide were determined spectrally and also from data on the kinetics of decomposition and azo coupling.The acidity of the phenylazobenzenediazonium ion, like that of the majority of organic cations, is higher than the H acidity of the diazohydroxide.The high equilibrium concentration and the high decomposition rate of this product, the presence of which was demonstrated experimentally, give rise to the extremely low stability of aqueous alkaline solutions of the phenylazobenzenediazonium salt.

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