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87764-37-2

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87764-37-2 Usage

Description

rac-Metalaxyl Carboxylic Acid is a derivative of Metalaxyl (M258740), a systemic fungicide with potent activity against various plant diseases.
Used in Agriculture:
rac-Metalaxyl Carboxylic Acid is used as a fungicide for controlling plant diseases such as downy mildew caused by Sclerospora framinicola and those caused by phycomycetes. Its application helps protect crops from these fungal infections, ensuring healthier growth and higher yields.

Check Digit Verification of cas no

The CAS Registry Mumber 87764-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,6 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 87764-37:
(7*8)+(6*7)+(5*7)+(4*6)+(3*4)+(2*3)+(1*7)=182
182 % 10 = 2
So 87764-37-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H19NO4/c1-9-6-5-7-10(2)13(9)15(11(3)14(17)18)12(16)8-19-4/h5-7,11H,8H2,1-4H3,(H,17,18)/t11-/m0/s1

87764-37-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(N-(2-methoxyacetyl)-2,6-dimethylanilino)propanoic acid

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:87764-37-2 SDS

87764-37-2Downstream Products

87764-37-2Relevant articles and documents

Elimination of racemic and enantioenriched metalaxyl based fungicides under tropical conditions in the field

Monkiedje, Adolphe,Zuehlke, Sebastian,Maniepi, Saurelle Jacqueline Ngouopiho,Spiteller, Michael

, p. 655 - 663 (2007)

The elimination has been studied of racemic and enantioenriched metalaxyl applied as an emulsifiable concentrate and wettable powder combined with copper in a Cameroonian field site. The kinetics of the degradation/dissipation of metalaxyl and its acid metabolite were investigated using reversed phase HPLC-MS/MS, while the enantiomeric ratios were measured by HPLC-MS/MS using a Chiralcel OD-H HPLC column. Some soil enzymes activities were determined concurrently for 120 d. The elimination of racemic metalaxyl was shown to be enantioselective, with the R-enantiomer being degraded more slowly than the S-enantiomer. Dissipation followed approximate square root first-order kinetics (R > 0.98) without lag phases. The enantiomers of metalaxyl have different elimination rates, with half-lives ranging from only 0.8 to 1.5 days. After application to soil, the elimination of metalaxyl in the copper containing formulation was slower. The activities of acid phosphatase, alkaline phosphatase, and alkaline glucosidase were monitored throughout the experiments. No significant influence of metalaxyl and copper could be observed on these parameters. The significantly shorter half-life values of all forms of metalaxyl under field conditions, compared to the previously reported laboratory derived ones, may have implications for the plant disease control with these fungicides in tropical rainforest areas.

Persistence, fate, and metabolism of [14C]metalaxyl in typical Indian soils

Sukul, Premasis,Spiteller, Michael

, p. 2352 - 2358 (2001)

The biodegradation of ring-labeled [14C]metalaxyl in six Indian soils was examined. The total recovery of radioactivity from soil was 100 ± 6% of the applied radioactivity. Volatile organics and 14CO2 were detected at lower levels. This suggests that neither mineralization nor volatilization is a major route of metalaxyl dissipation. The most rapid degradation of metalaxyl was observed in Bannimantap soil, in which the half-life of metalaxyl was 36 days. An inverse relationship was found when half-lives were plotted against microbial biomass and soil clay content. However, soil total organic carbon did not correlate with metalaxyl persistence. Five metabolites detected by thin-layer chromatography were more polar than metalaxyl.

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