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72431-61-9

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72431-61-9 Usage

Structure

Benzimidazole derivative with a carboxamide group and an amino group

Potential applications

Pharmaceutical industry (cancer and infectious disease drugs), agricultural chemicals

Additional potential uses and benefits

Under research and testing

Check Digit Verification of cas no

The CAS Registry Mumber 72431-61-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,3 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72431-61:
(7*7)+(6*2)+(5*4)+(4*3)+(3*1)+(2*6)+(1*1)=109
109 % 10 = 9
So 72431-61-9 is a valid CAS Registry Number.

72431-61-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1H-benzo[d]imidazole-1-carboxamide

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:72431-61-9 SDS

72431-61-9Downstream Products

72431-61-9Relevant articles and documents

Degradation of benomyl, picloram, and dicamba in a conical apparatus by zero-valent iron powder

Ghauch, Antoine

, p. 1109 - 1117 (2007/10/03)

Reduction of some pesticides (benomyl, picloram, and dicamba) was studied in an aerobic batch conical pilot system to investigate the disappearance of these pesticides on contact with iron powder (20 g/l, 325-mesh). Aqueous buffered solutions of the compounds were added to the system followed by zero-valent iron powder (ZVIP), and the decline in the pesticide concentrations was monitored over time. HPLC analyses show a complete disappearance of picloram (1.20 mg/l) after 20 min of reaction. Benomyl (1.00 mg/l) and dicamba (1.25 mg/l) disappear after 25 and 40 min, respectively. The t50 values ranged from 3 to 5.5 min, and were about slightly less than the t1/2 values reported when the log of the relative HPLC peak area was plotted versus time, where the relative peak area was calculated by dividing the measured peak area by the initial peak area. Pathways for the degradation of the studied pesticides by ZVIP are proposed.

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