페나미포스

페나미포스
페나미포스 구조식 이미지
카스 번호:
22224-92-6
한글명:
페나미포스
동의어(한글):
이소프로필포스포르아미드산에틸4-(메틸티오)-M-톨릴에스테르;페나미포스;(1-메틸에틸)포스포르아미드산 에틸 3-메틸-4-(메틸티오)페닐에스테르;(1-메틸에틸)포스포르아미드산, 에틸, 3-메틸-4-(메틸싸이오)페닐 에스터;N-(1-메틸에틸)포스포르아미드산, 에틸 3-메틸-4-(메틸싸이오)페닐 에스터;N-[에톡시-(3-메틸-4-메틸설판일페녹시)포스포릴]프로판-2-아민;아이소프로필포스포르아미드산, 에틸 4-(메틸싸이오)-m-톨릴 에스터;에틸 3-메틸-4-(메틸싸이오) 페닐(1-메틸에틸)포스포르아미데이트;에틸 4-(메틸싸이오)-m-톨릴 아이소프로필포스포르아미데이트;에틸-3-메틸-4-(메틸싸이오)페닐(1-메틸에틸)포스포르아미데이트
상품명:
Fenamiphos
동의어(영문):
PHENAMIPHOS;NEMACUR;sra3886;B 68138;Nenacur;SRA 3886;ent27572;nemacurp;BAY 68138;ai3-27572
CBNumber:
CB7215702
분자식:
C13H22NO3PS
포뮬러 무게:
303.36
MOL 파일:
22224-92-6.mol

페나미포스 속성

녹는점
49°C
끓는 점
375.6±52.0 °C(Predicted)
밀도
1.14
증기압
1.2 x 10-4 Pa (20 °C)
인화점
100 °C
저장 조건
0-6°C
용해도
클로로포름(약간 용해됨), 메탄올(약간 용해됨)
산도 계수 (pKa)
-0.09±0.70(Predicted)
물리적 상태
액체
색상
갈색
수용성
0.07g/100mL
Merck
13,3984
BRN
4752893
노출 한도
OSHA PEL: TWA 0.1 mg/m3; ACGIH TLV: TWA 0.1 mg/m3.
LogP
4.01 at 30℃
CAS 데이터베이스
22224-92-6(CAS DataBase Reference)
NIST
Fenamiphos(22224-92-6)
EPA
Fenamiphos (22224-92-6)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 T+;N,N,T+
위험 카페고리 넘버 24-28-50/53-36-26/28
안전지침서 23-28-36/37-45-60-61-35-26
유엔번호(UN No.) UN 2811/3017
WGK 독일 3
RTECS 번호 TB3675000
위험 등급 6.1(a)
포장분류 I
유해 물질 데이터 22224-92-6(Hazardous Substances Data)
독성 LD50 orally in rats (mg/kg): 10-25 (Waggoner, Khasawinah); LD50 orally in birds (mg/kg): 2.4 (Hill, Camardese)
기존화학 물질 KE-05-0608
유해화학물질 필터링 97-1-328
함량 및 규제정보 물질구분: 유독물질; 혼합물(제품)함량정보: 페나미포스 및 이를 1% 이상 함유한 혼합물
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H410 장기적 영향에 의해 수생생물에 매우 유독함 수생 환경유해성 물질 - 만성 구분 1 경고 GHS hazard pictograms P273, P391, P501
예방조치문구:
P262 눈, 피부, 의복에 묻지 않도록 하시오.
P273 환경으로 배출하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.

페나미포스 C화학적 특성, 용도, 생산

개요

Fenamiphos is a colorless crystalline substance. Solubility in water is 400 mg/L (20 ?C). It is soluble in polar organic solvents. Log Kow = 3.3(20 ?C). It is stable in aqueous media; DT50 (22 ?C) at pH 4, 7, and 9 are 1, 8, and 3 yr.

화학적 성질

Fenamiphos is a colorless crystal or a tan, waxy solid. It is non-corrosive to metals and breaks down readily in strong acids and bases. Fenamiphos is used as a nematicide and an insecticide. It is sparingly soluble in water, but readily soluble in dichloromethane, isopropanol, and toluene. It is used primarily for the control of nematodes and thrips on citrus, grapes, peanuts, pineapples, tobacco, turf, and ornamentals. There are no residential uses for fenamiphos. The US EPA has grouped fenamiphos as an RUP owing to its high acute toxicity and toxicity to wildlife. Reports have indicated that the manufacture and sale of fenamiphos is to be phased out by 2007–2008.

용도

Fenamiphos is primarily used to control nematodes in a wide range of crops and in turf. It will also control mites and sucking insects in crops.

일반 설명

Brown waxy solid or colorless solid. Used as a nematocide.

공기와 물의 반응

Fenamiphos is hydrolyzed by strong acids and strong alkalis.

반응 프로필

Organothiophosphates, such as Fenamiphos, are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.

위험도

Toxic by inhalation and skin contact. Questionable carcinogen.

건강위험

Fenamiphos is highly toxic orally, by inhalation, and by absorption through the skin. (Non-Specific -- Parathion) Death may occur from respiratory failure.

화재위험

(Non-Specific -- Organophosphorus Pesticide, n.o.s.) Container may explode in heat of fire. Fire and runoff from fire control water may produce irritating or poisonous gases. Emits toxic fumes of nitrogen oxides, phosphorus oxides, and sulfur oxides when heated to decomposition.

농업용

Nematicide, Insecticide: A U.S. EPA restricted Use Pesticide (RUP). Fenamiphos is an organophosphate nematicide used to control a wide variety of nematode (roundworm) pests. Nematodes can live as parasites on the outside or the inside of a plant. They may be free living or associated with cyst and root-knot formations in plants. Fenamiphos is used on a variety of plants including tobacco, turf, bananas, pineapples, citrus and other fruit vines, some vegetables, and grains. The compound is absorbed by roots and is then distributed throughout the plant. Fenamiphos, as is typical of other organophosphates, blocks the enzyme acetylcholinesterase in the target pest. The pesticide also has secondary activity against other invertebrates such as sucking insects and spider mites.

상품명

BAY 68138®; Bayer 68138®; NEMACUR®; NEMACURP®

Safety Profile

Poison by ingestion, inhalation, and skin contact. When heated to decomposition it emits very toxic fumes of NOx, POx, and SOx.

환경귀착

Soil. Oxidizes in soil to the corresponding sulfone and sulfoxide (Lee et al., 1986). Fenamiphos rapidly degraded in Arredondo soil to fenamiphos sulfone and at the sametime to the corresponding phenol. The half-life in this soil is 38–67 days (Ou and Rao, 1986).
Surface Water. In estuarine water, the half-life of fenamiphos was 1.80 days (Lacorte et al., 1995).
Chemical/Physical. Emits toxic fumes of phosphorus, nitrogen and sulfur oxides when heated to decomposition (Sax and Lewis, 1987; Lewis, 1990).

신진 대사 경로

Fenamiphos is an effective nematicide with both protectant and curative action. Free-living, ecto- and endo-parasitic, cyst-forming and root knot nematodes are controlled. Foliarly applied compound is translocated in plants to the roots and there is evidence that both translocation and optimum anti-cholinesterase and nematicide activity require oxidation of the thiomethyl group to the sulfoxide or the sulfone. These thiooxidation products are much more easily hydrolysed than fenamiphos itself and hydrolytic degradation in the environment most probably occurs via the formation of these intermediates.

신진 대사

The oxidation of the thiomethyl group to the sulfoxide and sulfone is required for both translocation and nematicidal activity in plants. The oxidation products are more susceptible to hydrolysis than fenamiphos itself. In mammals, orally administered fenamiphos is rapidly metabolized to the sulfoxide and sulfone, followed by subsequent hydrolysis, conjugation, and excretion in the urine. N-Dealkylation also occurs. The DT50 in soils is several weeks; the major degradation products are fenamiphos sulfoxide and sulfone and their phenols.

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