| Identification | Back Directory | [Name]
PENTANOCHLOR | [CAS]
2307-68-8 | [Synonyms]
CMMP
Solan
Dutom
Hortox
Solane
Dakuron
fmc4512
FMC 4512
Chlorpentan
niagara4512
Pentachlore
Niagara 4512
PENTANOCHLOR
Pentanochlore
CMMP Standard
CROPTEX BRONZE
Solan (Herbicide)
solan (wssa,exansi)
Pentanochlor solution
pentanochlor (bsi,iso)
PENTANOCHLOR PESTANAL
Pentanochlor Solution, 100ppm
3'-Chloro-2-methyl--toluidide
Chloro-2-methyl-p-valerotoluidide
Pentanochlor@100 μg/mL in Methanol
3-chloro-2-methylvaler-p-toluidide
3’-chloro-2-methyl-p-valerotoluidid
3’-chloro-2-methyl-p-valerotoluidide
3'-Chloro-2-methyl-p-valerotoluidide
p-Valerotoluidide, 3'-chloro-2-methyl-
N-(3-chloro-p-tolyl)-2-methylvaleramide
PENTANOCHLOR PESTANAL(N-(3-CHLORO-4-MET&
Chloro-4-(methylphenyl)-2-methylpentamide
N-(3-Chlor-methylphenyl)-2-methylpentanamid
N-(3-Chloro-4-methylphenyl)-2-methylvaleramide
n-(3-chloro-4-methylphenyl)-2-methyl-pentanamid
N-(3-Chloro-4-methylphenyl)-2-methylpentanamide
2-Methylenetanoic acid 4-methyl-3-chloropanylide
pentanamide,N-(3-chloro-4-methylphenyl)-2-methyl- | [EINECS(EC#)]
218-988-9 | [Molecular Formula]
C13H18ClNO | [MDL Number]
MFCD00145081 | [MOL File]
2307-68-8.mol | [Molecular Weight]
239.74 |
| Chemical Properties | Back Directory | [Appearance]
Solid. Insoluble in water; sol-
uble in pine oil, diisobutyl ketone, isophorone, and
xylene. Combustible.
| [Melting point ]
79-80° | [Boiling point ]
210°C (rough estimate) | [density ]
1.0747 (rough estimate) | [refractive index ]
1.6330 (estimate) | [storage temp. ]
2-8°C | [pka]
14.11±0.70(Predicted) | [Water Solubility ]
8.5mg/L(room temperature) | [EPA Substance Registry System]
Pentanochlor (2307-68-8) |
| Hazard Information | Back Directory | [Chemical Properties]
Solid. Insoluble in water; sol-
uble in pine oil, diisobutyl ketone, isophorone, and
xylene. Combustible.
| [Uses]
Herbicide. | [Definition]
ChEBI: Pentanochlor is an anilide. | [Production Methods]
The production of pentanochlor typically involves the acylation of a substituted aniline, specifically 3-chloro-4-methylaniline, with 2-methylpentanoic acid or its activated derivative such as an acid chloride. This reaction forms the amide bond central to pentanochlor’s structure, yielding N-(3-chloro-4-methylphenyl)-2-methylpentanamide. The process is carried out under controlled conditions using an organic solvent and a base to neutralise the byproduct (usually HCl if an acid chloride is used). After the reaction, the crude product is purified through recrystallisation or chromatography to achieve the desired purity for agricultural use. | [Mechanism of action]
Selective with contact action. Photosynthetic electron transport inhibitor at the photosystem II. | [Enzyme inhibitor]
This photosynthetic electron transport inhibitor (FW = 239.74 g/mol; CAS 2307-68-8), also known as Solan?, (RS)-3’-chloro-2-methylvaler-ptoluidide, and N-(3-chloro-4-methylphenyl)-2-methylpentanamide, is a selective pre- and post-emergence herbicide used to control annual weeds in fields producing carrots, celery, fennel, and parsley. Pentanochlor is also used in contact sprays with flowers and ornamental plants | [Pesticide Type]
Herbicide |
|
| Company Name: |
Energy Chemical
|
| Tel: |
400-0056266 |
| Website: |
www.energy-chemical.com |
|