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53112-28-0

53112-28-0 Structure

53112-28-0 Structure
IdentificationMore
[Name]

Pyrimethanil
[CAS]

53112-28-0
[Synonyms]

2-AMINOPHENYL-4,6-DIMETHYLPYRIMIDINE
2-ANILINO-4,6-DIMETHYLPYRIMIDINE
4,6-DIMETHYL-N-PHENYL-2-PYRIMIDINAMINE
4,6-DIMETHYL-N-PHENYL-PYRIMIDIN-2-AMINE
MYTHOS
N-(4,6-DIMETHYL-2-PYRIMIDINYL)-N-PHENYLAMINE
N-PHENYL-4,6-DIMETHYL-2-PYRIMIDINAMINE
PYRIMETHANIL
SCALA
2-anilin-4,6-dimethylpyrimidine
n-(4,6-dimethylpyrimidin-2-yl)aniline
Mytho
PYRIMETHANIL PESTANAL, 250 MG
2-Pyrimidinamine, 4,6-dimethyl-N-phenyl-
4,6-DIMETHYL-N-PHENYL-2-PYRIMIDINAMINE(PYRIMETHANIL)
Dynmethanil
[EINECS(EC#)]

414-220-3
[Molecular Formula]

C12H13N3
[MDL Number]

MFCD00172113
[Molecular Weight]

199.25
[MOL File]

53112-28-0.mol
Chemical PropertiesBack Directory
[Appearance]

Pyrimethanil is a white to light yellow crystal- line powder. Commercial product is available as a brown emulsifiable concentrate.
[Melting point ]

96°C
[Boiling point ]

362.8±45.0 °C(Predicted)
[density ]

1.15
[vapor pressure ]

2.2 x l0-5 Pa (25 °C)
[storage temp. ]

0-6°C
[solubility ]

DMSO: 130 mg/mL (652.45 mM)
[form ]

neat
[pka]

3.52
[Water Solubility ]

0.121 g/L (25 ºC)
[BRN ]

151589
[CAS DataBase Reference]

53112-28-0(CAS DataBase Reference)
[EPA Substance Registry System]

53112-28-0(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

N
[Risk Statements ]

R51/53:Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment .
[Safety Statements ]

S60:This material and/or its container must be disposed of as hazardous waste .
[RIDADR ]

UN 3077
[WGK Germany ]

2
[HS Code ]

2933599590
[Hazardous Substances Data]

53112-28-0(Hazardous Substances Data)
[Toxicity]

LD50 (mg/kg): 4061-5358 orally in mice; 4150-5971 orally in rats; >5000 dermally in rats; LC50 (96 hr) in mirror carp, rainbow trout (mg/l): 35.36, 10.56 (Neumann)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

2-MERCAPTOBENZYL ALCOHOL
[Preparation Products]

Pyrimethanil suspension
Hazard InformationBack Directory
[Potential Exposure]

A pyrimidine fungicide used on grapes, strawberries, tomatoes, onions, beans, cucumbers, eggplant, and ornamental plants.
[First aid]

If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 minutes, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions) if breathing has stopped, and CPR if heart action has stopped. Transfer promptly to a medical facility. When this chemical has been swallowed, get medical attention. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit.
[Shipping]

UN3082 Environmentally hazardous substances, liquid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required. UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required.
[Incompatibilities]

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explo- sions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides.
[Chemical Properties]

Off-White Solid
[Chemical Properties]

Pyrimethanil is a white to light yellow crystal- line powder. Commercial product is available as a brown emulsifiable concentrate.
[Waste Disposal]

Containers must be disposed of properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office. If this material cannot be disposed of according to label instruc- tions, it may be dissolved or mixed with a combustible sol- vent and burned in a chemical incinerator equipped with an afterburner and scrubber. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers.
[Uses]

Fungicide.
[Uses]

Pyrimethanil is a broad spectrum anilino-pyrimidine foliar fungicide. Pyrimethanil functions by inhibiting the biosynthesis of methionine in Botrytis cinerea.
[Uses]

Pyrimethanil provides both protective and curative control of fungal diseases in pome fruits (leaf scab caused by Venturiu inaequalis), vines, fruits, vegetables and ornamentals (grey mould)
[Definition]

ChEBI: A member of the class of aminopyrimidines that is N-phenylpyrimidin-2-amine carrying two additional methyl substituents at positions 4 and 6. A fungicide used to control grey mould on fruit, vegetables and ornamentals as well as leaf sc b on pome fruit. Also commonly employed to control Botrytis cinerea throughout the winemaking process in grapes, must, fermenting must and wine.
[Preparation]

Pyrimethanil is produced by reaction of 2-bromo-4,6-dimethylpyrimidine with aniline.
[Synthesis Reference(s)]

Chemical and Pharmaceutical Bulletin, 30, p. 1942, 1982 DOI: 10.1248/cpb.30.1942
[General Description]

Pyrimethanil is an anilino-pyrimidine, broad spectrum fungicide primarily used for the control of gray mould and leaf scab on fruits, vegetables and ornamentals. Its mode of action involves inhibition of the secretion of hydrolytic enzymes by the fungi during the infection process, thus stopping the further development of the disease.
[Agricultural Uses]

Fungicide: Used on grapes, strawberries, tomatoes, onions, beans, cucumbers, eggplant, and ornamental.
[Trade name]

SCALA®; SN 100309®
[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, 1995). Hydroxylation at the methyl, phenyl or pyrimidine moiety is the primary metabolic pathway of pyrimethanil in soil, plants and animals. Cleavage of the aniho-pyrimidine linkage was observed as a minor metabolic reaction. The formation of nitro- analogues of pyrimethanil is a novel nitration reaction observed in the soil metabolism study (Scheme 1).
[Degradation]

Pyrimethanil (1) is stable to hydrolytic degradation in the environmentally relevant pH range (5-9) at 22-50 °C.
Pyrimethanil degraded rapidly at pH 4 and 30 °C (DT50 1 day) when the sterile buffered solution was exposed to mercury arc lamp (200-500 nm). The DT50 of pyrimethanil in pH 7 solution under the same photolysis test conditions was ca.77 days. There is no information on the chemical nature of pyrimethanil aqueous photolysis products.
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

53112-28-0(sigmaaldrich)
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