테플루쓰린

한글명:테플루쓰린

카스 번호79538-32-2

상품명:Tefluthrin

CBNumberCB7211825

분자식C17H14ClF7O2

포뮬러 무게418.73

MOL 파일79538-32-2.mol

동의어(한글)

테플루쓰린

테플루트린

(1R,3R)-rel-3-[(1Z)-2-클로로-3,3,3-트라이플루오로-1-프로펜-1-일]-2,2-다이메틸사이클로프로페인카복실산, (2,3,5,6-테트라플루오로-4-메틸페닐)메틸 에스터

화학적 성질

녹는점	44-46°C
끓는 점	bp1.33hPa 156°
밀도	1.23
증기압	8×10^-3 Pa (20 °C)
저장 조건	0-6°C
용해도	클로로포름(약간 용해됨), 메탄올(약간 용해됨)
수용성	0.02mg l^-1(20°C)
Merck	13,9192
BRN	8398039
LogP	6.500
EPA	Tefluthrin (79538-32-2)

위험 및 안전 성명

위험품 표기	T+
위험 카페고리 넘버	23/24-28
안전지침서	22-28-36/37/39-45
유엔번호(UN No.)	UN 3349
WGK 독일	3
RTECS 번호	GZ1227850
위험 등급	6.1(a)
포장분류	I
HS 번호	29162090
유해 물질 데이터	79538-32-2(Hazardous Substances Data)
독성	LD50 technical grade in rats (mg/kg): 35 orally; 200-1000 dermally (Marrs, Gordon)

그림문자(GHS)

테플루쓰린 화학적 특성, 용도, 생산

화학적 성질
Pale Yellow Low Melting Solid
용도
Tefluthrin is a pyrethroid based insecticide. Tefluthrin is used in the control of a broad range of soil pests, including members of the Coleoptera, Lepidoptera, and Diptera.
정의
ChEBI: A cyclopropanecarboxylate ester resulting from the formal condensation of the carboxy group of 3-[(1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylic acid with the hydroxy group of 2,3,5,6-tetrafluoro-4-methylbe zyl alcohol.
농업용
Insecticide, Miticide: A U.S. EPA restricted use Pesticide (RUP). Registered in the U.S. for use on corn. Elsewhere it is registered for use on a variety of crops, e.g., peanuts, sweet potato, sugarcane, cabbage, radish, Brussels sprouts, and strawberries. Registered for use in EU countries.
상품명
FORCE®; FORCE® ST; FORZA®; JF 6064®; KOMET-RP®; PP 993®; R 151993®
Pharmacology
The commercialized compound, tefluthrin, was recommended to control soil-inhabiting pests (28). The most salient feature of the compound, which justifies its use exclusively for better performance of tefluthrin as a soil insecticide compared with cyhalothrin, is its approximately four orders ofmagnitude higher vapor pressure (V.P. = 8.4 vs. 0.001 mPa; see Table 6). Beside the quick insecticidal action attributed to fast penetration, tefluthrin also displays toxic symptoms at its sublethal dose, which could play an important role in field performance (179). The most active configuration of tefluthrin, (Z)(1RS)-cis-isomer mixture, is the optically active (Z)(1R)-cis-isomer.
신진 대사 경로
When a goat is dosed with 14C-tefluthrin orally, extensive metabolism occurs in the goat by ester cleavage and oxidation at a variety of positions on the molecules. Low radioactive residues are detected in the milk, fat, and muscle, with tefluthrin as the largest individual component of the residue. Higher residues are present in the kidney and liver, and only a small percentage of this residue is due to tefluthrin. The remainder in the kidney and liver is a complex mixture of metabolites. In total, eight metabolites are identified in the feces and urine as well as other tissues such as fat, muscle, kidney, and liver.

테플루쓰린 준비 용품 및 원자재

테플루쓰린 관련 검색

Send Inquriy