안트라센

안트라센
안트라센 구조식 이미지
카스 번호:
120-12-7
한글명:
안트라센
동의어(한글):
안트라센;p-나프탈렌;안트라신;파라나프탈렌
상품명:
Anthracene
동의어(영문):
Anthracen;Antracene;GREEN OIL;Anthracence;1,2-DIBROMOETHANE, 1X1ML, MEOH, 5000UG/M L;jingen;CI 10790;NSC 7958;antracen;ANTHRACIN
CBNumber:
CB7375466
분자식:
C14H10
포뮬러 무게:
178.23
MOL 파일:
120-12-7.mol
MSDS 파일:
SDS

안트라센 속성

녹는점
210-215 °C (lit.)
끓는 점
340 °C (lit.)
밀도
1.28
증기 밀도
6.15 (vs air)
증기압
1 mm Hg ( 145 °C)
굴절률
1.5948
인화점
121 °C
저장 조건
2-8°C
용해도
톨루엔: 용해성20mg/mL, 투명, 무색 내지 희미한 노란색
산도 계수 (pKa)
>15 (Christensen et al., 1975)
물리적 상태
가루
색상 색인 번호
10790
색상
황백색에서 노란색까지
폭발한계
0.6%(V)
수용성
0.045mg/L(25℃)
Merck
14,682
BRN
1905429
Henry's Law Constant
1.22 at 4 °C, 6.42 at 25 °C (dynamic equilibrium method, Bamford et al., 1999)
Dielectric constant
2.3500000000000001
노출 한도
OSHA: TWA 0.2 mg/m3
LogP
4.65 at 20℃
CAS 데이터베이스
120-12-7(CAS DataBase Reference)
IARC
3 (Vol. 92, Sup 7) 2010
NIST
Anthracene(120-12-7)
EPA
Anthracene (120-12-7)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi,N,F,T,Xn
위험 카페고리 넘버 36/37/38-50/53-67-36-11-39/23/24/25-23/24/25-65-38-66-51/53
안전지침서 26-60-61-24/25-16-9-45-36/37-62-36
유엔번호(UN No.) UN 3077 9/PG 3
WGK 독일 2
RTECS 번호 CA9350000
자연 발화 온도 540 °C
TSCA Yes
위험 등급 9
포장분류 III
HS 번호 29029010
유해 물질 데이터 120-12-7(Hazardous Substances Data)
독성 LD50 orally in Rabbit: > 16000 mg/kg
기존화학 물질 KE-01825
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
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:
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
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.
P337+P313 눈에 대한 자극이 지속되면 의학적인 조치· 조언를 구하시오.
P391 누출물을 모으시오.
NFPA 704
1
1 0

안트라센 MSDS


Anthraxcene

안트라센 C화학적 특성, 용도, 생산

개요

세고리 방향족 탄화수소다.벤젠 고리 3개가 일렬로 붙어서 14개의 π전자를 갖게 되어 분자가 방향족성을 띈다.

용도

나프탈렌과는 달리 더 길어진 π시스템의 영향으로 자외선을 받으면 보라색 형광을 내기 시작한다. 콜타르에서 발견되며, 유기분자 주제에 반도체 성질을 띄기 때문에 염료나 유기광전자소자의 반도체 재료의 유도체로 사용된다.

개요

Anthracene is one of a group of chemicals called polycyclic aromatic hydrocarbons (PAHs). PAHs are often found together in groups of two ormore. They can exist inmore than 100 different combinations, but the most common are treated as a group of 15. PAHs are found naturally in the environment but they can also be made synthetically. Anthracene can vary in appearance from a colorless to pale yellow crystal-like solid. PAHs are created when products like coal, oil, gas, and garbage are burned but the burning process is not complete. Very little information is available on the individual chemicals within the PAH group; the majority of the information is for the entire PAH group. Anthracene is a solid white to yellow crystal, has a weak aromatic odor, and sinks in water. Its characteristics are boiling point, 3421°C; melting point, 2181°C; molecular weight, 178.22; density/specific gravity, 1.25 at 27 and 41°C; octanol–water coefficient, 4.45. It is soluble in absolute alcohol and organic solvents. Maximum absorption occurs at 218 nm.

화학적 성질

Anthracene is colorless, to pale yellow crystalline solid with a bluish fluorescence. PAHs are compounds containing multiple benzene rings and are also called polynuclear aromatic hydrocarbons.

물리적 성질

White to yellow crystalline flakes or crystals with a bluish or violet fluorescence and a weak aromatic odor. Impurities (naphthacene, tetracene) impart a yellowish color with green fluorescence.

용도

Anthracene is an aromatic hydrocarbonwith three fused rings, and is obtained by the distillationof crude oils. The main useis in the manufacture of dyes.It is an important source of dyestuffs.

정의

(C14H10) A white crystalline solid used extensively in the manufacture of dyes. Anthracene is found in the heavy- and green-oil fractions of crude oil and is obtained by fractional crystallization. Its structure is benzene-like, having three six-membered rings fused toanion gether. The reactions are characteristic of AROMATIC COMPOUNDS.

생산 방법

Anthracene is obtained from coal tar in the fraction distilling between 300° and 400 °C. This fraction contains 5–10% anthracene, from which, by fractional crystallization followed by crystallization from solvents, such as oleic acid, and washing with such solvents as pyridine, relatively pure anthracene is obtained. It may be detected by the formation of a blue-violet coloration on fusion with mellitic acid. Anthracene derivatives, especially anthraquinone, are important in dye chemistry.

화학 반응

Anthracene reacts: (1) With oxidizing agents, e.g., sodium dichromate plus sulfuric acid, to form anthraquinone, C6H4(CO)2C6H. (2) With chlorine in water or in dilute acetic acid below 250 °C to form anthraquinol and anthraquinone, at higher temperatures 9,10-dichloroanthracene. The reaction varies with the temperature and with the solvent used. The reaction has been studied using, as solvent, benzene, chloroform, alcohol, carbon disulfide, ether, glacial acetic acid, and also without solvent by heating. Bromine reacts similarly to chlorine. (3) With concentrated sulfuric acid to form various anthracene sulfonic acids. (4) With nitric acid, to form nitroanthracenes and anthraquinone. (5) With picric acid (1)HO·C6H2(NO2)3(2,4,6) to form red crystalline anthracene picrate, melting point 138 °C.

일반 설명

White to yellow solid with a weak aromatic odor. Sinks in water.

공기와 물의 반응

Flammable. Insoluble in water.

반응 프로필

Anthracene will spontaneously burst into flame on contact with chromic acid, and other strong oxidants.

위험도

A questionable carcinogen.

건강위험

Carcinogenicity of anthracene is not known.Its toxicity is very low. An intraperitonealLD50 in mice is recorded at 430 mg/kg(NIOSH 1986).

화재위험

Anthracene is combustible.

Safety Profile

Moderately toxic by intraperitoneal route. A skin irritant and allergen. Questionable carcinogen with experimental neoplas tigenic and tumorigenic data. Mutation data reported. Combustible when exposed to heat, flame, or oxidizing materials. Moderately explosive when exposed to flame, Ca(OCl)z, chromic acid. To fight fire, use water, foam, CO2, water spray or mist, dry chemical. Explodes on contact with fluorine.

잠재적 노출

It is used as an intermediate in dye stuffs (alizarin), insecticides, and wood preservatives; making synthetic fibers, anthraquinone, and other chemicals. May be present in coke oven emissions, diesel fuel, and coal tar pitch volitiles.

Carcinogenicity

Anthracene was negative in mouse-skin-painting studies, and it is classified as a noncarcinogen by the IARC based on inadequate evidence. The methyl, anthryl, dimethyl, diprophyl, dinaphthyl, and tetramethyl derivatives of anthracene were noncarcinogenic except for 9,10-dimethyl anthracene, which may have contained impurities when tested.

운송 방법

UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

비 호환성

Finely dispersed powder may form explosive mixture in air. Contact with strong oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides, chromic acid/or calcium hypochlorite.

폐기물 처리

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. Incineration.

안트라센 준비 용품 및 원자재

원자재

준비 용품


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