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S-metolachlor CAS 87392-12-9 178961-20-1

Place of Origin: Zhejiang,China (Mainland)
Type: Liquid
Brand Name: MOSINTER
CAS No.: 87392-12-9 178961-20-1
Name: s-Metochlor
Molecular Weight: 283.7937
Molecular Formula: C15H22ClNO2
Density: 1.101g/cm3
Flash point: 199.837°C
Boiling point: 406.819°C at 760 mmHg
Refractive index: 1.533
Vapour Pressur: 0mmHg at 25°C
Water solubility: 530mg/kg(20℃)
  • 87392-12-9

  • MOSINTER

  • 87392-12-9

Availability:
Product Description

Payment & Shipping Terms

Supply Capacity

Payment Terms:

T/T, WU

Production Capacity:

500T/year

Min. Order:

25KG

Packing:

according to the customer's requirements 

Means of Transport:

Ocean, Air, Land

Delivery Date:

7 days

 

S-Metolachlo CAS: 87392-12-9 178961-20-1 is an organic compound that is widely used as an herbicide.


S-Metolachlor Attribute

Molecular Formula

C15H22ClNO2

Molecular Weight

283.7937

Density

1.101g/cm3

Boiling point

406.819°C at 760 mmHg

Refractive index

1.533

Flash point

199.837°C

Vapour Pressur

0mmHg at 25°C

 

It is a derivative of aniline and is a member of the chloroacetanilide herbicides.It is highly effective toward grasses but its application is also controversial.

 

Agricultural use of S-Metolachlo CAS No. 87392-12-9 178961-20-1

Its acts by inhibition of elongases and of the geranylgeranyl pyrophosphate (GGPP) cyclases, which are part of the gibberellin pathway. It is used for grass and broadleaf weed control in corn, soybean, peanuts, sorghum, and cotton. It is also used in combination with other herbicides.

 

Metolachlor is a popular herbicide in the United States. Metolachlor is becoming less and less common. As originally formulated metolachlor was applied asa racemate, a 1:1 mixture of the (S)- and (R)-stereoisomers. The (R)-enantiomer is inactive, and modern production methods afford only (S)-metolachlor, thus current application rates are far lower than original formulations.


Production and basic structure

Metolachlor is produced from 2-ethyl-6 methylaniline (MEA) via condensation with methoxyacetone. 

The resulting imine is hydrogenated to give primarily the S-stereoisomeric amine. This secondary amine is acetylated with chloroacetylchloride. Because of the steric effects of the 2,6-disubstituted aniline, rotation about the aryl-C to N bond is restricted. Thus, for both the (R)- and the (S)-enantiomers exist as atropisomers. Both atropisomers of (S)-metolachlor exhibit the same biological activity.

 

Safety and Ecological Effects

Metolachlor has been detected in ground and surface waters in concentrations ranging from 0.08 to 4.5 parts per billion (ppb) throughout the U.S.

 

It is classified as a Category C pesticide by the United States Environmental Protection Agency (US EPA),which indicates limited evidence of carcinogenicity.

 

Evidence of the bioaccumulation of metolachlor in edible species of fish as well as its adverse effect on the growth and development raise concerns on its effects on human health. Though there is no set maximum concentration (maximum contaminant level, MCL) for metolachlor that is allowed in drinking water, the US EPA does have a health advisory level (HAL) of 0.525 mg/L.

 

Metolachlor induces cytotoxic and genotoxic effects in human lymphocytes. Genotoxic effects have also been observed in tadpoles exposed to metolachlor. Evidence also reveals that metolachlor affects cell growth. Cell division in yeast was reduced, and chicken embryos exposed to metolchlor showed a significant decrease in the average body mass compared to the control.


Mosinter, a professional Herbicides Farm Chemicals manufacturer in China, produces high quality S-Metolachlo CAS: 87392-12-9 178961-20-1. 

 


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