Fenpropidin
Fenpropidin Basic information
- Product Name:
- Fenpropidin
- Synonyms:
-
- TERN
- SPONSOR
- 1-(3-(4-(1,1-dimethylethyl)phenyl)-2-methylpropyl)-piperidin
- 1-(3-(4-(1,1-dimethylethyl)phenyl)-2-methylpropyl)piperidine
- 1-(3-(4-tert-butylphenyl)-2-methylpropyl)piperidine
- cga114900
- fenpropidine
- patrol
- CAS:
- 67306-00-7
- MF:
- C19H31N
- MW:
- 273.46
- Product Categories:
-
- Alpha sort
- E-GAlphabetic
- F
- FA - FLPesticides
- Fungicides
- Others
- Pesticides&Metabolites
- Mol File:
- 67306-00-7.mol
Fenpropidin Chemical Properties
- Melting point:
- 25°C
- Boiling point:
- bp0.2 117°; bp0.045 125°; bp0.032 104°
- Density
- 0.9112 (rough estimate)
- vapor pressure
- 1.7 x 10-2 Pa (25 °C)
- refractive index
- 1.4900 (estimate)
- storage temp.
- Refrigerator
- solubility
- Chloroform, Ethyl Acetate (Slightly)
- pka
- 10.1
- Water Solubility
- 530 mg l-1 (pH 7 at 25 °C)
- color
- Clear Colourless
- Merck
- 13,4020
- BRN
- 5336091
- CAS DataBase Reference
- 67306-00-7
- NIST Chemistry Reference
- Fenpropidin(67306-00-7)
- EPA Substance Registry System
- Piperidine, 1-[3-[4-(1,1-dimethylethyl)phenyl]-2-methylpropyl]- (67306-00-7)
Fenpropidin Usage And Synthesis
Description
fenpropidine, a piperidine derivative, and spiroxamine, a dioxolanemethyleneamine derivative introduced in 1996 , belong to the same group of fungicides.
Uses
Fenpropidin is a fungicide.
Uses
Agricultural fungicide.
Uses
Fenpropidin is both a contact and a systemic fungicide which provides effective eradicant control of powdery mildew, rusts and leaf blotch in cereal.
Definition
ChEBI: A member of the class of piperidines that is N-isobutylpiperidine in which a hydrogen of one of the methyl groups is replaced by a p-tert-butylphenyl group.
Hazard
Moderately toxic by ingestion, inhalation, and skin contact.
Metabolic pathway
Limited data are available in the open literature. Information presented in this summary is abstracted from the data evaluation published by the Pesticide Safety Directorate (PSD, 1993). Fenpropidin is stable to aqueous hydrolysis and photodegradation. Hydroxylation of the piperidine ring is the primary metabolic pathway in soil and wheat plants. Hydroxylation and oxidation of one of the methyl groups of the tert-butyl moiety are the major reactions in rats and lactating goats. The primary metabolic pathways of fenpropidin are presented in Scheme 1.
Degradation
Fenpropidin (1)i s stable to hydrolytic degradation (50 °C)in the pH range of 3-9 and when exposed to UV light in pH 5 buffer solution.
FenpropidinSupplier
- Tel
- 010-82848833 400-666-7788
- jkinfo@jkchemical.com
- Tel
- info@syntechem.com
- Tel
- 400-1166-196 18981987031
- cdhxsj@163.com
- Tel
- 400-6206333 18521732826;
- market@aladdin-e.com
- Tel
- 025-57798810
- sales@sunlidabio.com