| Company Name: |
J & K SCIENTIFIC LTD.
|
| Tel: |
18210857532; 18210857532 |
| Email: |
jkinfo@jkchemical.com |
| Products Intro: |
Product Name:Azafenidin
CAS:68049-83-2
Package:10Mg,1Mg
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- Azafenidin
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- $2500.00 / 100mg
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2025-04-30
- CAS:68049-83-2
- Min. Order:
- Purity:
- Supply Ability: 10g
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| | azafenidin Basic information |
| Product Name: | azafenidin | | Synonyms: | 2-(2,4-dichloro-5-prop-2-ynyloxyphenyl)-5,6,7,8-tetrahydro-1,2,4-triazole(4,3-a)pyridin-3(2H)-one;azafenidin;Evolus;Milestone;2-(2,4-dichloro-5-prop-2-ynyloxypnenyl)-5,6,7,8-tetrahy-dro-1,2,4-trizolo [4,3-α] pyridin-3-(2H)-one;DPX-R 6447;IN-R 6447;R 6447 | | CAS: | 68049-83-2 | | MF: | C15H13Cl2N3O2 | | MW: | 338.19 | | EINECS: | | | Product Categories: | Agro-Products, Aromatics, Heterocycles | | Mol File: | 68049-83-2.mol |  |
| | azafenidin Chemical Properties |
| Melting point | 168-168.5° | | Boiling point | 468.9±55.0 °C(Predicted) | | density | 1.43±0.1 g/cm3(Predicted) | | solubility | DMSO (Slightly), Methanol (Slightly) | | form | Solid | | pka | 2.45±0.20(Predicted) | | color | Brown to Dark Brown | | EPA Substance Registry System | Azafeniden (68049-83-2) |
| Hazard Codes | T,N | | Risk Statements | 61-48/22-62-50/53 | | Safety Statements | 53-45-60-61 | | Toxicity | LD50 in rats, mice, bobwhite quail, mallard duck (mg/kg): >5000, >5000, >2500, >2500 orally; in rabbits (mg/kg): >2000 dermally.; LC50 in rats, rainbow trout, blue gill sunfish (mg/l): >5.3, 33, 48 (Amuti) |
| | azafenidin Usage And Synthesis |
| Uses | Azafenidin is a weed controlling herbicide used in various crops. | | Uses | Herbicide. | | Definition | ChEBI: Azafenidin is a triazolopyridine that is 5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one which is substituted at position 2 by a 2,4-dichloro-5-(prop-2-yn-1-yloxy)phenyl group. A protoporphyrinogen oxidase inhibitor, it is used as a herbicide to control weeds in fruit crops such as pineapple, citrus, melons, and grapes. Not approved for use within the European Union. It has a role as an EC 1.3.3.4 (protoporphyrinogen oxidase) inhibitor. It is a triazolopyridine, a terminal acetylenic compound and a dichlorobenzene. | | Metabolic pathway | A common degradation reaction of azafenidin in light,
plants and soil is O-dealkylation, and interesting minor
reactions in soil are the subsequent methylation of the
O-dealkylated degradation product and the reduction
of the propynyl group under anaerobic conditions. In
soil and light, azafenidin is also readily split to form
the triazolinone heterocycle. Azafenidin is readily
metabolized in rats and lactating goats through
O-dealkylation, hydroxylation of the triazolinone ring
in several positions, and glucuronide and sulfate
conjugation. |
| | azafenidin Preparation Products And Raw materials |
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