| Identification | Back Directory | [Name]
Sulcotrione | [CAS]
99105-77-8 | [Synonyms]
SC0051
MIKADO
GALLEON
ICIA0051
SULCOTRIONE
CHLORMESULON
Sulcotrione 0
Sulcotrione 95%
SULCOTRIONE,MESOTRIONE
Sulcotrione@100 μg/mL in Methanol
Sulcotrione Solution in Methanol, 100μg/mL
2-(2-chloro-4-mesylbenzoyl)cyclohexane-1,3-dione
2-(2-Chlor-4-(methylsulfonyl)-benzoyl)-1,3-cyclohexandion
2-(2-chloro-4-(methylsulfonyl)benzoyl)-1,3-cyclohexanwdione
1,3-Cyclohexanedione,2-(2-chloro-4-methanesulfonylbenzoyl)-
2-(2-chloro-4-(methylsulfonyl)benzoyl)-1,3-cyclohexanedione
1,3-Cyclohexanedione, 2-[2-chloro-4-(methylsulfonyl)benzoyl]- | [EINECS(EC#)]
278-636-5 | [Molecular Formula]
C14H13ClO5S | [MDL Number]
MFCD01632349 | [MOL File]
99105-77-8.mol | [Molecular Weight]
328.77 |
| Chemical Properties | Back Directory | [Melting point ]
139° | [Boiling point ]
574.5±50.0 °C(Predicted) | [density ]
1.428±0.06 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Room Temperature | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
neat | [pka]
3.22±0.50(Predicted) | [color ]
White to off-white | [Merck ]
13,8979 | [BRN ]
8155739 | [Henry's Law Constant]
1.7×106 mol/(m3Pa) at 25℃, Maniere et al. (2011) | [Major Application]
agriculture
environmental | [InChI]
1S/C14H13ClO5S/c1-21(19,20)8-5-6-9(10(15)7-8)14(18)13-11(16)3-2-4-12(13)17/h5-7,13H,2-4H2,1H3 | [InChIKey]
PQTBTIFWAXVEPB-UHFFFAOYSA-N | [SMILES]
CS(=O)(=O)c1ccc(c(Cl)c1)C(=O)C2C(=O)CCCC2=O | [EPA Substance Registry System]
1,3-Cyclohexanedione, 2-[2-chloro-4-(methylsulfonyl) benzoyl]-(99105-77-8) |
| Hazard Information | Back Directory | [Uses]
Herbicide. | [Definition]
ChEBI: An aromatic ketone that is cyclohexane-1,3-dione substituted by a 2-chloro-4-(methylsulfonyl)benzoyl group at position 2. | [Production Methods]
Sulcotrione is commercially produced via a multi-step process starting with the Friedel-Crafts acylation of 1,2,4-trichlorobenzene with 2-chloropropionyl chloride using aluminium chloride to form 2-chloro-1-(2,4,5-trichlorophenyl)propan-1-one, which undergoes intramolecular cyclization under basic conditions to yield the benzoyl cyclohexanedione core; subsequent oxidation with air or sulphur in the presence of a base introduces the sulfonyl group, producing the compound. | [Mechanism of action]
Absorbed mainly by the leaves but also some root uptake. Bleaching: inhibition of 4-hydroxyphenyl-pyruvate-dioxygenase. | [Pharmacology]
Mode of action studies with sulcotrione first led to the
identity of HPPD as a highly effective herbicide target
site. Early observations showed that a related compound
caused increased levels of tyrosine in the plasma and urine
of treated rats (12). Further studies showed that one of the
tyrosine catabolism enzymes, 4-hydroxypyruvate dioxygenase,
was inhibited by cyclohexanediones (13,14)—this
enzyme being required for the formation of quinones, such
as plastoquinone in plants (12,15,16). Inhibition results in
the perturbation of carotenoid synthesis and inhibition of
photosynthetic electron transport (16). | [Metabolism]
Sulcotrione is readily absorbed through the leaves and
via the roots. In the soil, metabolism involves ring opening
of the cyclohexanedione, eventually to give the
corresponding benzoic acid (17) and, finally, CO2 (8).
In the soil, the half-life of sulcotrione can vary
considerably (between 15 days in loamy sand and 72 days
in fine loam), depending on a number of factors, especially
the soil organic matter content (18,19). | [Pesticide Type]
Herbicide |
|
| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
|