Mepronil

Mepronil

Mepronil

Min.Order / FOB Price:Get Latest Price

1 Kilogram

FOB Price: USD 30.0000

  • Min.Order :1 Kilogram
  • Purity: 99%
  • Payment Terms : L/C,T/T,

Keywords

55814-41-0 Mepronil Mepronil

Quick Details

  • Appearance:Powder
  • Application:intermediate
  • PackAge:as per buyers
  • ProductionCapacity:1|Metric Ton|Day
  • Storage:R.T.
  • Transportation:by air/sea

Superiority:

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3.OLED intermediates (Fluorene,Carbazole,Boric acid...)
4.Customs Synthesis
 
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Details:

Product Name: Mepronil
Synonyms: 2-methyl-n-(3-(1-methylethoxy)phenyl)-benzamid;b1-2459;Benzamide, 2-methyl-N-(3-(1-methylethoxy)phenyl)-;kco-1;N-(3-Isopropoxyphenyl)-2-methylbenzamide;BASITAC;BASITAC(R);MEPRONIL
CAS: 55814-41-0
MF: C17H19NO2
MW: 269.34
EINECS:
Product Categories: FUNGICIDE
Mol File: 55814-41-0.mol
Mepronil Structure
Mepronil Chemical Properties
Melting point  84-89°C
Boiling point  412.48°C (rough estimate)
density  1.0483 (rough estimate)
vapor pressure  5.6 x 10-5 Pa (20 °C)
refractive index  1.5400 (estimate)
storage temp.  0-6°C
Water Solubility  12 mg l-1(20 °C)
form  neat
pka 13.10±0.70(Predicted)
BRN  2381749
CAS DataBase Reference 55814-41-0(CAS DataBase Reference)
NIST Chemistry Reference Mepronil(55814-41-0)
EPA Substance Registry System Mepronil (55814-41-0)
Safety Information
WGK Germany  2
RTECS  CV5581700
HS Code  29242990
Toxicity LD50 oral in rabbit: > 10gm/kg
MSDS Information
Mepronil Usage And Synthesis
Uses Mepronil is an benzanilide based fungicide found in the raw materials of herbal medicine.
Uses Mepronil is used to control Basidiomycetes diseases in rice, cereals, potatoes, vegetables, sugar beet, fruit, vines, tobacco, turf grass and other crops.
Definition ChEBI: A member of the class of benzamides, obtained by formal condensation of the carboxy group of 2-methylbenzoic acid with the amino group of 3-(ispropyloxy)aniline. A fungicide used to control diseases caused by Basidomycetes including Rhizoctonia
Metabolic pathway Mepronil is an analogue of flutolanil containing a 2-methyl group as opposed to the 2-trifluoromethyl group. The compounds have the same mode of action and are metabolised via similar routes except that the methyl group of mepronil provides an extra site for metabolic attack. The compound is metabolised by dealkylation and hydroxylation at both the methyl and isopropyl groups and by aryl hydroxylation. Some hydrolysis occurs in plants and animals.

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