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18108-16-2

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18108-16-2 Usage

General Description

Phosphinic acid, phenylmethyl ester, also known as PMIDA, is an organophosphorus compound used as a pesticide and herbicide. Its chemical formula is C8H11O2P and it is a colorless liquid with a slightly fruity odor. PMIDA is used in a variety of agricultural settings to control weeds and pests, and is often formulated as a water-soluble concentrate. However, it is considered to be toxic to aquatic life and can have negative effects on non-target organisms. PMIDA is typically handled with protective equipment and its use is regulated in many countries due to its potential environmental and human health impacts.

Check Digit Verification of cas no

The CAS Registry Mumber 18108-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,0 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18108-16:
(7*1)+(6*8)+(5*1)+(4*0)+(3*8)+(2*1)+(1*6)=92
92 % 10 = 2
So 18108-16-2 is a valid CAS Registry Number.

18108-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name phosphorosooxymethylbenzene

1.2 Other means of identification

Product number -
Other names Phosphinic acid,phenylmethyl ester

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:18108-16-2 SDS

18108-16-2Upstream product

18108-16-2Relevant articles and documents

Synthesis of H-Phosphonate Intermediates and Their Use in Preparing the Herbicide Glyphosate

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Paragraph 0044; 0036, (2014/10/16)

The esterfication of hypophosphorous acid is followed by reaction with another molecule of alcohol under the action of a nickel catalyst to provide a green method for the preparation of H-phosphonate diesters. This method avoids the need for any stoichiometric chlorine unlike those based on phosphorous trichloride.

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