3-(4-클로로페닐)-1,1-디메틸요소

3-(4-클로로페닐)-1,1-디메틸요소
3-(4-클로로페닐)-1,1-디메틸요소 구조식 이미지
카스 번호:
150-68-5
한글명:
3-(4-클로로페닐)-1,1-디메틸요소
동의어(한글):
3-(4-클로로페닐)-1,1-디메틸요소;모누론;1-(4-클로로페닐)-3,3-다이메틸유레아;1-(p-클로로페닐)-3,3-다이메틸유레아;1,1-다이메틸-3-(4-클로로페닐)유레아;1,1-다이메틸-3-(p-클로로페닐)유레아;1-p-클로로페닐-3,3-다이메틸유레아;3-(p-클로로페닐)-1,1-다이메틸유레아;3-p-클로로페닐-1,1-다이메틸유레아;N'-(4-클로로페닐)-N,N-다이메틸유레아;n-(4-클로로페닐)-N',N'-다이메틸유레아;N'-(4-클로로페닐)-N,N-디메틸우레아;N-p-클로로페닐-N',N'-다이메틸유레아
상품명:
MONURON
동의어(영문):
CMU;Telvar;CMU(R);MONURON;Monurex;karmexw;Monurox;rosuran;chlorea;usafp-8
CBNumber:
CB4706609
분자식:
C9H11ClN2O
포뮬러 무게:
198.65
MOL 파일:
150-68-5.mol
MSDS 파일:
SDS

3-(4-클로로페닐)-1,1-디메틸요소 속성

녹는점
173-174 °C (lit.)
끓는 점
301.31°C (rough estimate)
밀도
1,27 g/cm3
증기압
0Pa at 20℃
굴절률
1.5330 (estimate)
저장 조건
0-6°C
산도 계수 (pKa)
14.22±0.70(Predicted)
물리적 상태
결정질 고체
색상
하얀색
수용성
262mg/L(25℃)
최대 파장(λmax)
244nm(H2O)(lit.)
Merck
14,6261
BRN
2097922
LogP
1.94 at 20℃
IARC
3 (Vol. Sup 7, 53) 1991
EPA
Monuron (150-68-5)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,N
위험 카페고리 넘버 22-40-50/53
안전지침서 36/37-60-61
유엔번호(UN No.) UN 3077 9/PG 3
WGK 독일 3
RTECS 번호 YS6300000
TSCA Yes
위험 등급 9
포장분류 III
HS 번호 29242990
유해 물질 데이터 150-68-5(Hazardous Substances Data)
독성 LD50 orally in rats: 3700 mg/kg (Bailey, White)
기존화학 물질 2008-2-28
그림문자(GHS): GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
H351 암을 일으킬 것으로 의심됨 (노출되어도 암을 일으키지 않는다는 결정적인 증거가 있는 노출경로가 있다면 노출경로 기재) 발암성 물질 구분 2 경고 P201, P202, P281, P308+P313, P405,P501
H410 장기적 영향에 의해 수생생물에 매우 유독함 수생 환경유해성 물질 - 만성 구분 1 경고 GHS hazard pictograms P273, P391, P501
예방조치문구:
P202 모든 안전 조치 문구를 읽고 이해하기 전에는 취급하지 마시오.
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P270 이 제품을 사용할 때에는 먹거나, 마시거나 흡연하지 마시오.
P273 환경으로 배출하지 마시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.
P308+P313 노출 또는 접촉이 우려되면 의학적인 조치· 조언를 구하시오.
NFPA 704
0
2 0

3-(4-클로로페닐)-1,1-디메틸요소 C화학적 특성, 용도, 생산

화학적 성질

White, crystalline solid; odorless. Very low solubility in water and hydrocarbonsolvents; slightly soluble in oils; partially soluble inalcohols; stable toward oxidation and moisture.

용도

Monuron may be used as a reference standard in the determination of monuron in rice and corn using high performance liquid chromatography coupled with fluorescence detection combined with ultraviolet decomposition and post-column derivatization.

정의

ChEBI: A member of the class of ureas that is urea in which one of the nitrogens is substituted by a p-chlorophenyl group while the other is substituted by two methyl groups.

일반 설명

White crystalline solid or white powder with a slight odor. Melting point 175°C. Moderately toxic by ingestion. Used as an herbicide.

공기와 물의 반응

Insoluble in water. Is hydrolyzed slowly by acids and alkalis, and more rapidly on heating .

반응 프로필

MONURON is a chlorinated urea derivative. May react with azo and diazo compounds to generate toxic gases. May react with strong reducing agents to generate flammable gases. Reacts as a weak base. Combustion generates mixed oxides of nitrogen (NOx).

위험도

Questionable carcinogen.

건강위험

Toxic properties are similar to Diuron; hydro-lyzes under acidic or alkaline conditions top-chloroaniline, which can cause anemia andmethemoglobinemia; LD50 data published inthe literature differ; acute and chronic tox-icity of this herbicide is probably of loworder; no reported case of human poisoning; showed clear evidence of carcinogenicity in male F344/N rats fed diets containing 750 ppm monuron for 2 years; causedcancers in the kidney and liver (NationalToxicology Program 1988); female rats andmale and female mice (B6C3F1) showed noevidence; induced cytomegaly of the renalepithelial cells in rats.
LD50 oral (rat): 3700 mg/kg (Bailey andWhite, 1965)
LD50 oral (rat): 1053 mg/kg (Lewis 1995).

화재위험

Flash point data for MONURON are not available; however, MONURON is probably combustible.

Safety Profile

Moderately toxic by ingestion, intraperitoneal, and possibly other routes. Experimental teratogenic and reproductive effects. Questionable carcinogen with experimental carcinogenic data. Mutation data reported. An herbicide. When heated to decomposition it emits very toxic fumes of NOx and Cl-.

환경귀착

Biological. Monuron was mineralized in sewage samples obtained from a water treatment plant in Ithica, NY. (4-Chlorophenyl)urea and 4-chloroaniline were tentatively identified as metabolites (Wang et al., 1985).
Soil/Plant. In soils and plants, monuron is demethylated at the terminal nitrogen atom coupled with ring hydroxylation forming 3-(2-hydroxy-4-chlorophenyl)urea and 3-(3- hydroxy-4-chlorophenyl)urea (Hartley and Kidd, 1987). Walln?efer et al. (197
Photolytic. When an aqueous solution of monuron was exposed to sunlight or simulated sunlight, the major degradative pathways observed were the photooxidation and demethylation of the N-methyl groups (Crosby and Tang, 1969; Tanaka et al., 1982a),
Tanaka et al. (1981) studied the photolysis of monuron in dilute aqueous solutions in order to fully characterize a substituted diphenylamine that was observed in an earlier investigation (Tanaka et al., 1977). They identified this compound as an isomeric mixture containing 92% 2-chloro-4¢,5-bis(N¢,N¢-dimethylureido)biphenyl and 8% 5-chloro-2,4¢- bis(N¢,N¢-dimethylureido)biphenyl (Tanaka et al., 1981).
Tanaka et al. (1982) undertook a study to identify the several biphenyls formed in earlier photolysis studies (Tanaka et al., 1979, 1981). They identified these compounds as 2,4¢-, 3,4¢- and 4,4¢-bis-(N¢,N¢-dimethylureido)biphenyls (fenuron biphenyls) (Ta

Purification Methods

Crystallise monuron from MeOH. [Beilstein 12 IV 1191.]

3-(4-클로로페닐)-1,1-디메틸요소 준비 용품 및 원자재

원자재

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3-(4-클로로페닐)-1,1-디메틸요소 공급 업체

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