Grundinformationen
- Standard-SMILES
N#Cc1c[nH]cc1-c1cccc(Cl)c1Cl- InChIKey
FKLFBQCQQYDUAM-UHFFFAOYSA-N- Summenformel
- C11H6Cl2N2
- Durchschnittliche Molmasse
- 237,08 g/mol
- Monoisotopische Masse
- 235,99080355
Überblick
Fenpiclonil is a member of the class of pyrroles carrying cyano and 2,3-dichlorophenyl substituents at positions 3 and 4 respectively. A fungicide used mainly to control seed-borne pathogens in cereal crops. It has a role as an antifungal agrochemical. It is a nitrile, a dichlorobenzene and a member of pyrroles.
Namen und Bezeichner
- Bevorzugter Name
- Fenpiclonil
- IUPAC
- 4-(2,3-dichlorophenyl)-1H-pyrrole-3-carbonitrile
- Englischer Name
- FENPICLONIL
- Summenformel
- C11H6Cl2N2
- Molmasse
- 237.08
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
74738-17-3- PubChem CID
- 91724
- DTXSID
DTXSID0036633- ChEMBL
CHEMBL1770195- ChEBI
CHEBI:34759- UNII
- 21OCB8KDQ9
- EC Number
- 616-132-2
- Nikkaji
- J470.032E
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 4,3
- Polarare Oberfläche (TPSA)
- 39,6 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 1
- Frei drehbare Bindungen
- 1
- Schwere Atome
- 15
- Formalladung
- 0
- Komplexität
- 273
Experimentelle und physikochemische Eigenschaften
Pesticides
Fungicides
Active substance -> EU Pesticides database: Not approved
Physikochemische Eigenschaften
- Schmelzpunkt
- 152.9 ℃ · 152.9℃
- Siedepunkt
- 378.43 °C · 378.43°C (rough estimate)
- Dichte
- 1.4052 · 1.4052 (rough estimate)
- Dampfdruck
- 1.1 x · 1.1 x 10-7 Pa (25 °C)
- Brechungsindex
- 1.64 · 1.6400 (estimate)
- Wasserlöslichkeit
- 4.8 mg · 4.8 mg l-1 in water at 25 °C
- pka
- 13.63 · 13.63±0.50(Predicted)
- Merck
- 13 · 13,4016
- BRN
- 5433281 · 5433281
- Henry's Law Constant
- 1.8 · 1.8×103 mol/(m3Pa) at 25℃, Duchowicz et al. (2020)
- Major Application
- agricultureenvironmental
- InChI
- 1S/C11H6Cl2N2/c12-10-3-1-2-8(11(10)13)9-6-15-5-7(9)4-14/h1-3,5-6,15H
- InChIKey
- FKLFBQCQQYDUAM-UHFFFAOYSA-N
- SMILES
- Clc1cccc(c1Cl)-c2c[nH]cc2C#N
- EPA chemische Informationen
- 1 H-Pyrrole-3-carbonitrile, · 1H-Pyrrole-3-carbonitrile, 4-(2,3-dichlorophenyl)- (74738-17-3)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Warning
H332 (100%): Harmful if inhaled [Warning Acute toxicity, inhalation]
P261, P271, P304+P340, and P317 (click each P-code to see the statement)
Aggregated GHS information provided per 67 reports by companies from 1 notifications to the ECHA C&L Inventory.
Gefahrenhinweise
Regulatory Information
2002/2076
Fenpiclonil: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.
Sicherheitsdaten
- wgk
- 2
- ridadr
- 3077
- RTECS-Nr.
- UX9347500
- risk_code
- 20
- Toxizität
- LD50 in rats, mice, rabbits (mg/kg): >5000 orally; LD50 dermally in rats: >2000 mg/kg; LC50 (4 hr) in rats: >1502 mg/m3 by inhalation (Nevill)
- hazard_code
- Xn
- hazard_class
- 9
- packing_group
- III
- Speicherklasse
- 11 - Combustible Solids
- Hazard Classifications
- Acute Tox. 4 Inhalation
Chemie und Industrie
Verwendung und Herstellung
Anwendungen
BeschreibungFenpiclonil is the first phenylpyrrole fungicide developed by Ciba Geigy (now belonging to the portfolio of Syngenta Crop Protection AG) for seed treatment. Different formulation types have been used for its commercialization either in solo (trade name “Beret”) or in mixture with other fungicides, as for instance, imazalil (“Beret Special”) or carboxin + imazalil (“Beret Universal”).
VerwendenFenpiclonil is a systemic and contact fungicide that provides protective control of seed-borne pathogens of cereals such as snow mould and bunt caused by Fusarium spp., Tilletia caries, Septoria nodorum, etc. It also controls leaf spot, brown foot rot and ear blight in non-cereal crops.
Vor- und nachgelagerte Produkte
Vorgelagerte Rohstoffe
Anbieter17 Anbieter
Ergänzende Hinweise
DefinitionChEBI: A member of the class of pyrroles carrying cyano and 2,3-dichlorophenyl substituents at positions 3 and 4 respectively. A fungicide used mainly to control seed-borne pathogens in cereal crops.
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