프로피콘아졸 C화학적 특성, 용도, 생산
개요
Propiconazole is a mixture of four stereoisomers and was first
developed in 1979 by Janssen Pharmaceutical of Belgium.
화학적 성질
normally provided as a yellow liquid
용도
Labelled Propiconazole (P770100). Systemic foliar fungicide. Agricultural fungicide.
일반 설명
Yellowish odorless liquid. Non corrosive. Used as a fungicide.
반응 프로필
A triazole derivative.
농업용
Fungicide: Used to control fungi on a broad range of crops and turf. Used on ornamentals, range land and rights-of-way to prevent and control powdery mildew and fungi on hardwoods and conifers.
상품명
ALAMO®; BANNER®; BENIT®; BREAK®; BUMPER®; CGA-64250®; CGA-92710 F®; DESMEL®; FIDIS®; JUNO®; MANTI® S; MAXX®; NOVEL®; ORBIT®; PRACTIS®; PROPIMAX®; RADAR®; RESTORE®; SPIRE®; STRATEGO® (trifloxystrobin + propiconazole); TASPA®; TILT®; WOCOSIN®
잠재적 노출
Propiconazole is a triazole fungicide
used to control fungi on a broad range of crops and turf.
Used on ornamentals, range land and rights-of-way to pre-
vent and control powdery mildew and fungi on hardwoods
and conifers.
신진 대사 경로
The numerous metabolites of propiconazole are
identified from rat urine and feces. Major sites for
enzymatic attack are the propyl side chain and the
cleavage of the dioxane ring. The 2,4-dichlorophenyl
ring is attacked in various ways including the formation of a cyclohexadiene ring system, hydroxylation,
replacement of the chlorine substituent by a hydroxy
group, and introduction of a methylthio group. The
1,2,4-triazole ring is oxidatively attacked, leading to
hydroxy derivatives. The vast majority of the alcoholic
and phenolic metabolites are excreted as sulfuric acid
and glucuronic acid conjugates. The major metabolic
pathway in mice is via cleavage of the dioxane ring.
Photolysis causes cleavage of the C1-triazole bond of
propiconazole, liberating 1,2,4-triazole as the major
product. Six more degradation products are identified
which are not included in the mammalian metabolites.
운송 방법
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.
비 호환성
The triazoles are sensitive to heat,
friction, and impact. Sensitivity varies with the type
substitution to the triazole ring. Metal chelated and halogen
substitution of the triazol ring make for a particularly heat
sensitive material. Azido and nitro derivatives have been
employed as high explosives. No matter the derivative
these materials should be treated as explosives
폐기물 처리
Consult with environmental
regulatory agencies for guidance on acceptable disposal
practices. Contact a licensed disposal facility about surplus
and nonrecyclable solutions. Burn in a chemical incinerator
equipped with an afterburner and scrubber. Extra care must
be exercised as the material in an organic solvent is highly
flammable. In accordance with 40CFR165, follow recom-
mendations for the disposal of pesticides and pesticide con-
tainers. Containers must be disposed of properly by
following package label directions or by contacting your
local or federal environmental control agency, or by con-
tacting your regional EPA office. Incineration or permanga-
nate oxidation.
프로피콘아졸 준비 용품 및 원자재
원자재
준비 용품
