Basic information

Product Name: 1-Triazene, 3-butyl-1,3-bis(4-nitrophenyl)-
Synonyms:
CAS NO:59453-64-4
Molecular Formula: C16H17N5O4
Molecular Weight: 343.342
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-Triazene, 3-butyl-1,3-bis(4-nitrophenyl)-(CAS DataBase Reference)
NIST Chemistry Reference: 1-Triazene, 3-butyl-1,3-bis(4-nitrophenyl)-(59453-64-4)
EPA Substance Registry System: 1-Triazene, 3-butyl-1,3-bis(4-nitrophenyl)-(59453-64-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 59453-64-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 59453-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,4,5 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 59453-64:
(7*5)+(6*9)+(5*4)+(4*5)+(3*3)+(2*6)+(1*4)=154
154 % 10 = 4
So 59453-64-4 is a valid CAS Registry Number.

59453-64-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name	N-butyl-4-nitro-N-[(4-nitrophenyl)diazenyl]aniline

1.2 Other means of identification

Product number	-
Other names	1-Triazene,3-butyl-1,3-bis(4-nitrophenyl)

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).

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59453-64-4Relevant academic research and scientific papers

Contribution to the analysis of the hypoglycaemic agent tolbutamide. II

Oelschlaeger,Blume

, p. 581 - 584 (2007/10/02)

The chemical identification reaction for tolbutamide (USP 1975) involves its hydrolysis by sulphuric acid with the formation of n-butylamine. This amine then reacts with diazotised p-nitraniline to give 8 red or yellow coloured compounds. A radicalic and

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