m-디클로로벨젠

m-디클로로벨젠
m-디클로로벨젠 구조식 이미지
카스 번호:
541-73-1
한글명:
m-디클로로벨젠
동의어(한글):
1,3-다이클로로벤젠;m-다이클로로벤젠;m-디클로로벨젠;m-다이클로로벤젠(m-DICHLOROBENZENE)
상품명:
1,3-Dichlorobenzene
동의어(영문):
MDCB;M-DICHLOROBENZENE;1,3-Dichlorbenzol;1,3-dichlorbenzene;2,6-Dichlorobenzene;Metadichlorobenzene;NSC 8754;1,3-DichL;1.3-Dichlorobe;Fluralaner-008
CBNumber:
CB8853781
분자식:
C6H4Cl2
포뮬러 무게:
147
MOL 파일:
541-73-1.mol
MSDS 파일:
SDS

m-디클로로벨젠 속성

녹는점
-25--22 °C (lit.)
끓는 점
172-173 °C (lit.)
밀도
1.288 g/mL at 25 °C (lit.)
증기압
5 mm Hg ( 38.8 °C)
굴절률
n20/D 1.546(lit.)
인화점
146 °F
저장 조건
2-8°C
용해도
혼합하기가 어렵습니다.
물리적 상태
액체
색상
무색투명~미황색
냄새
기분 좋은 냄새
수용성
0.0123g/100mL(25℃)
어는점
-24℃
Merck
14,3055
BRN
956618
Henry's Law Constant
2.14 at 20.00 °C (inert gas stripping, Hovorka and Dohnal, 1997)
Dielectric constant
5.0
안정성
안정성 가연성. 강한 산화제, 알루미늄, 알루미늄 합금과 호환되지 않습니다. 습기에 민감합니다.
InChIKey
ZPQOPVIELGIULI-UHFFFAOYSA-N
LogP
3.53 at 22℃
CAS 데이터베이스
541-73-1(CAS DataBase Reference)
IARC
3 (Vol. 73) 1999
NIST
Benzene, 1,3-dichloro-(541-73-1)
EPA
m-Dichlorobenzene (541-73-1)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,N,T,F
위험 카페고리 넘버 22-51/53-39/23/24/25-23/24/25-11
안전지침서 61-45-36/37-16-7
유엔번호(UN No.) UN 3082 9/PG 3
WGK 독일 2
RTECS 번호 CZ4499000
자연 발화 온도 >500 °C
TSCA Yes
위험 등급 6.1(b)
포장분류 III
HS 번호 29036990
유해 물질 데이터 541-73-1(Hazardous Substances Data)
독성 LD50 orally in Rabbit: 580 mg/kg
기존화학 물질 KE-10067
그림문자(GHS): GHS 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
H411 장기적 영향에 의해 수생생물에 유독함 수생 환경유해성 물질 - 만성 구분 2
예방조치문구:
P273 환경으로 배출하지 마시오.
NFPA 704
2
2 0

m-디클로로벨젠 MSDS


1,3-Dichlorobenzene

m-디클로로벨젠 C화학적 특성, 용도, 생산

물리적 성질

1,3-Dichlorobenzene is a clear, colorless liquid with a disinfectant or musty-type odor. Soluble in alcohol, ether, insoluble in water. At 40 °C, the average odor threshold concentration and the lowest concentration at which an odor was detected were 170 and 177 μg/L, respectively. At 25 °C, the lowest concentration at which a taste was detected was 190 μg/L, respectively (Young et al., 1996).

용도

1,3-Dichlorobenzene is used in organic synthesis that can synthesize fungicides imazalil, propiconazole, epiconazole, and insecticides insectaphos. It is also used in the synthesis of 1,2-diaminobenzene, in addition, it is also used as a solvent in the fields of dyes, medicine, resin, rubber and so on.

용도

1,3-Dichlorobenzene is used in medicine, and dyes. And it is also used to study the effect of solvent vapor pressure on the vertical nanowire of C60 molecules1. 1,3-Dichlorobenzene, a chlorinated aromatic hydrocarbon, can be detected in environmental samples using an advanced Fourier transform infrared spectroscopy-attenuated total reflectance (FTIR-ATR) sensor.

정의

ChEBI: 1,3-dichlorobenzene is a dichlorobenzene carrying chloro substituents at positions 1 and 3. Used as a fumigant, insecticide, and chemical intermediate.

제조 방법

1,3-Dichlorobenzene is prepared from o-chloroaniline through diazotization and displacement reaction.
Add o-chloroaniline and hydrochloric acid into the reaction pot, mix evenly below 25°C, cool to 0°C, drop in sodium nitrite solution, control the temperature at 0-5°C, stop adding when the potassium iodide starch indicator turns blue, and obtain diazonium salt solution. Then add the diazonium salt solution into the hydrochloric acid solution of cuprous chloride at 0~5℃, stir well, heat up to 60~70℃ and react for 1h, after cooling, let stand for stratification, and use 5% sodium hydroxide for the oil layer. Repeated washing with water, dehydration with anhydrous calcium chloride, fractional distillation, and collection of fractions at 177-183 °C to obtain the product 1,3-dichlorobenzene.

일반 설명

Colorless liquid. Sinks in water.

공기와 물의 반응

1,3-Dichlorobenzene is sensitive to moisture. Insoluble in water.

반응 프로필

1,3-Dichlorobenzene is incompatible with oxidizing agents and aluminum and its alloys. Above the flash point, explosive vapor-air mixtures may be formed.

건강위험

INHALATION: Causes headache, drousiness, unsteadiness. Irritating to mucous membranes. EYES: Severe irritation. SKIN: Severe irritation. INGESTION: Irritation of gastric mucosa, nausea, vomiting, diarrhea, abdominal cramps and cyanosis.

화재위험

Special Hazards of Combustion Products: Irritating vapors including hydrogen chloride are produced.

Safety Profile

Moderately toxic by intraperitoneal route. Mutation data reported. When heated to decomposition it emits toxic fumes of Cl-. See also oDICHLOROBENZENE and p DICHLOROBENZENE.

잠재적 노출

The major uses of o-DCB are as a process solvent in the manufacturing of toluene diisocyanate and as an intermediate in the synthesis of dyestuffs, herbicides, and degreasers. p-Dichlorbenzene is used primarily as a moth repellant, a mildew control agent; space deodorant; and in insecticides, which accounts for 90% of the total production of this isomer. Information is not available concerning the production and use of m-DCB. However, it may occur as a contaminant of o-or p-DCB formulations. Both o-and p-isomers are produced almost entirely as by-products during the production of monochlorobenzene

환경귀착

Biological. When 1,3-dichlorobenzene was statically incubated in the dark at 25 °C with yeast extract and settled domestic wastewater inoculum, significant biodegradation with gradual acclimation was followed by a deadaptive process in subsequent subcultures. At a concentration of 5 mg/L, 59, 69, 39, and 35% losses were observed after 7, 14, 21, and 28-d incubation periods, respectively. At a concentration of 10 mg/L, percent losses were virtually unchanged. After 7, 14, 21, and 28-d incubation periods, percent losses were 58, 67, 31, and 33, respectively (Tabak et al., 1981).
Photolytic. The sunlight irradiation of 1,3-dichlorobenzene (20 g) in a 100-mL borosilicate glass-stoppered Erlenmeyer flask for 56 d yielded 520 ppm trichlorobiphenyl (Uyeta et al., 1976).
Chemical/Physical. Anticipated products from the reaction of 1,3-dichlorobenzene with atmospheric ozone or OH radicals are chlorinated phenols, ring cleavage products, and nitro compounds (Cupitt, 1980). Based on an assumed base-mediated 1% disappearance after 16 d at 85 oC and pH 9.70 (pH 11.26 at 25 oC), the hydrolysis half-life was estimated to be >900 yr (Ellington et al., 1988). 1,3-Dichlorobenzene (0.17–0.23 mM) reacted with OH radicals in water (pH 8.7) at a rate of 5.0 x 109/M·sec (Haag and Yao, 1992).

운송 방법

m-DCB: UN2810 Toxic liquids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required. United States DOT Regulated Marine Pollutant. UN3077 Environmentally hazardous substances, solis, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical NameRequired. UN3082 Environmentally hazardous substances, liquid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required

Purification Methods

Wash it with aqueous 10% NaOH, then with water until neutral, dry and distil it. Conductivity material (ca 10-10 mhos) has been prepared by refluxing over P2O5 for 8hours, then fractionally distilling, and storing with activated alumina. m-Dichlorobenzene dissolves rubber stoppers. [Beilstein 5 IV 657.]

비 호환성

For o-DCB and m-DCB: acid fumes, chlorides, strong oxidizers; hot aluminum, or aluminum alloys. For p-DCB: Strong oxidizers; although, incompatibilities for this chemical may also include other materials listed for o-DCB.

폐기물 처리

Incineration, preferably after mixing with another combustible fuel. Care must be exercised to assure complete combustion to prevent the formation of phosgene. An acid scrubber is necessary to remove the halo acids produced. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal

m-디클로로벨젠 준비 용품 및 원자재

원자재

준비 용품


m-디클로로벨젠 공급 업체

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