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피리프로시펜

피리프로시펜
피리프로시펜 구조식 이미지
카스 번호:
95737-68-1
한글명:
피리프로시펜
동의어(한글):
피리프로시펜;피리프록시펜
상품명:
Pyriproxyfen
동의어(영문):
s9138;s31183;S 9318;SK-591;LANO(R);ADEAL(R);KNACK(R);SUMILARV;OMS-3019;JUVINAL(R)
CBNumber:
CB2779692
분자식:
C20H19NO3
포뮬러 무게:
321.37
MOL 파일:
95737-68-1.mol

피리프로시펜 속성

녹는점
45-47°C
끓는 점
230-250 °C(Press: 0.2 Torr)
밀도
1.32
증기압
2.9 x l0-4 Pa (20 °C)
굴절률
nD20.5 1.5823
저장 조건
0-6°C
물리적 상태
neat
산도 계수 (pKa)
3.2 (base, est.)
수용성
0.4 mg l-1 (25 °C)
InChIKey
NHDHVHZZCFYRSB-UHFFFAOYSA-N
CAS 데이터베이스
95737-68-1(CAS DataBase Reference)
NIST
Pyriproxyfen(95737-68-1)
EPA
Pyriproxyfen (95737-68-1)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 N
위험 카페고리 넘버 50/53
안전지침서 60-61
유엔번호(UN No.) UN3077 9/PG 3
WGK 독일 2
RTECS 번호 UT5804000
위험 등급 9
포장분류 III
유해 물질 데이터 95737-68-1(Hazardous Substances Data)
독성 LD50 oral in rat: > 5gm/kg
기존화학 물질 97-3-404
그림문자(GHS):
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H410 장기적 영향에 의해 수생생물에 매우 유독함 수생 환경유해성 물질 - 만성 구분 1 경고 P273, P391, P501
예방조치문구:
P273 환경으로 배출하지 마시오.
P501 ...에 내용물 / 용기를 폐기 하시오.

피리프로시펜 MSDS


2-(1-Methyl-2-(4-phenoxyphenoxy)ethoxy)pyridine

피리프로시펜 C화학적 특성, 용도, 생산

개요

Pyriproxyfen is a pyridine compound and, in common with fenoxycarb, is a juvenile hormone mimic whose structure is unrelated to natural juvenile hormone. It is an insect growth regulator. Fleas absorb pyriproxyfen either by direct contact or by ingesting blood from a treated animal.

화학적 성질

Gray to white crystalline solid or powder. Also described as a pale yellow, waxy solid or liquid. Commercial product is available as an emulsifiable concen- trate or wettable powders.

용도

Pyriproxyfen is a pyridine-based pesticide used against a variety of arthropoda, in particular to protect cotton crops against whitefly.

용도

Insecticide.

용도

Pyriproxyfen is used for control of public health pests (flies, beetles, midges, mosquitoes) by application to breeding sites.

정의

ChEBI: An aromatic ether that consists of propylene glycol having a 2-pyridyl group at the O-1 position and a 4-phenoxyphenyl group at the O-3 position.

농업용

Insect growth regulator, Insecticide, Veterinary medicine: Pyriproxyfen is found in a number of household products as sprays, powders, baits, mists and shampoos for the control of fleas, ticks, mites and flying insects on pets, in the air, and in carpets and rugs. It’s a larvicidal agent that mimics juvenile insect hormone.

상품명

ARCHER®; DALAR®; DISTANCE®; ESTEEM®; NYLAR®; S-9318®; S 31183®; SUMILARV® Pyriproxyfen

잠재적 노출

Pyriproxyfen is an unclassified insect growth regulator, insecticide, veterinary medicine found in a number of household products as sprays, powders, baits, mists and shampoos for the control of fleas, ticks, mites, and flying insects on pets, in the air, and in carpets and rugs. It’s a l larvicidal agent that mimics juvenile insect hormone.

신진 대사 경로

Pyriproxyfen is not persistent in soils and sediments and is rapidly metabolised by a variety of organisms. In rats and mice, the major metabolic pathways were hydroxylation of the aromatic ring, hydroxylation at the 5-position of the pyridyl ring, loss of the aromatic ring, cleavage of ether linkages and conjugation of the resultant phenols with glucuronic or sulfuric acid. The general pathways in soils, sediments and a variety of organisms involve fission of ether linkages and hydroxylation of the phenoxyphenol group.

운송 방법

UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous haz- ardous material, Technical Name Required.

Degradation

[14C]Pyriproxyfen was dissolved in distilled water or sterile river water at a concentration of 0.2 mg kg-1 and exposed to natural sunlight from November to December at 40°N latitude. The DT50 values were 17.5 and 21 days in distilled water and sterile river water respectively. Photodegradation involved cleavage at the three ether linkages and the major products were carbon dioxide (11-29% of the applied radioactivity) and a product formed by loss of the phenoxyphenyl group (9) (16-30%). When [14C]pyriproxyfen was exposed to sunlight for 8 weeks on sandy loam and silty loam soils, the DT50 values were 11 and 13 weeks respectively. Photodegradation involved cleavage at the three ether linkages to give products 4,6 and 10 but the major product was carbon dioxide, representing 9.5-13% of the applied radioactivity. Bound radioactivity accounted for 11-26% of the applied radioactivity at week 8 (Miyamoto et al., 1993). Degradation products are shown in Scheme 1.

비 호환성

This material is combustible. Dust may form an explosive mixture in air. Incompatible with oxidi- zers (chlorates, nitrates, peroxides, permanganates, perchlo- rates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides.

폐기물 처리

It is the responsibility of chemical waste generators to determine the toxicity and physical properties and of a discarded chemical and to properly identify its classification and certification as a hazardous waste and to determine the disposal method. United States Environmental Protection Agency guidelines for the classification determination are listed in 40 CFR Parts 261.3. Additionally, waste generators must consult and follow all regional, national, state and local hazardous waste laws to ensure complete and accurate classification and disposal methods. Follow recommendations for the disposal of pesticides and pesticide containers. 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.

피리프로시펜 준비 용품 및 원자재

원자재

준비 용품


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