크리센

크리센
크리센 구조식 이미지
카스 번호:
218-01-9
한글명:
크리센
동의어(한글):
크리센
상품명:
Chrysene
동의어(영문):
CHRYSEN;[4]Phenacene;BENZO[A]PHENANTHRENE;1,2-Benzophenanthrene;⋲Crysene;Chrycene;NSC 6175;CHRYSENE;Chrysene,98%
CBNumber:
CB9853344
분자식:
C18H12
포뮬러 무게:
228.29
MOL 파일:
218-01-9.mol
MSDS 파일:
SDS

크리센 속성

녹는점
252-254 °C (lit.)
끓는 점
448 °C (lit.)
밀도
1.274
증기압
4.3 at 25 °C (de Kruif, 1980)
굴절률
1.7480 (estimate)
인화점
-17℃
저장 조건
Store below +30°C.
용해도
<0.0001g/l
색상
White to Light yellow to Light orange
수용성
불용성
Merck
14,2255
BRN
1909297
Henry's Law Constant
1.97, 6.91, 18.8, 52.3, and 118 at 4.1, 11.0, 18.0, 25.0, and 31.0 °C, respectively (Bamford et al., 1998)
안정성
안정적인. 타기 쉬운. 강한 산화제와 호환되지 않습니다.
InChIKey
WDECIBYCCFPHNR-UHFFFAOYSA-N
CAS 데이터베이스
218-01-9(CAS DataBase Reference)
IARC
2B (Vol. 92) 2010
NIST
Chrysene(218-01-9)
EPA
Chrysene (218-01-9)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 T,N,Xn,F
위험 카페고리 넘버 45-50/53-68-40-67-66-36-11-52/53-36/37/38
안전지침서 53-45-60-61-36/37-26-16-24/25-23
유엔번호(UN No.) UN 3077 9/PG 3
WGK 독일 3
RTECS 번호 GC0700000
위험 등급 9
포장분류 III
HS 번호 29029090
유해 물질 데이터 218-01-9(Hazardous Substances Data)
독성 Acute LC50 for Neanthes arenaceodentata >50 μg/L (Rossi and Neff, 1978).
기존화학 물질 KE-05-0357
중점관리물질 필터링 별표2-47
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
H341 유전적인 결함을 일으킬 것으로 의심됨 (노출되어도 생식세포 유전독성을 일으키지 않는다는 결정적인 증거가 있는 노출경로가 있다면 노출경로 기재) 생식세포 변이원성 물질 구분 2 경고 P201,P202, P281, P308+P313, P405,P501
H350 암을 일으킬 수 있음 (노출되어도 암을 일으키지 않는다는 결정적인 증거가 있는 노출경로가 있다면 노출경로 기재) 발암성 물질 구분 1A, 1B 위험 GHS hazard pictograms
H410 장기적 영향에 의해 수생생물에 매우 유독함 수생 환경유해성 물질 - 만성 구분 1 경고 GHS hazard pictograms P273, P391, P501
예방조치문구:
P201 사용 전 취급 설명서를 확보하시오.
P273 환경으로 배출하지 마시오.
P308+P313 노출 또는 접촉이 우려되면 의학적인 조치· 조언를 구하시오.
NFPA 704
0
1 0

크리센 C화학적 특성, 용도, 생산

화학적 성질

Chrysene is a combustible, white (when pure), red, or blue, fluorescent crystalline solid. Odorless. Chrysene 859 Polycyclic aromatic hydrocarbons (PAHs) are compounds containing multiple benzene rings and are also called polynuclear aromatic hydrocarbons

물리적 성질

Orthorhombic, bipyramidal plates from benzene exhibiting strong reddish-blue fluorescence under UV light

용도

Chrysene may be used as an analytical reference standard for the determination of the analyte in fish bile, air particulate extracts and food samples by various chromatography techniques.

일반 설명

A crystalline solid. Denser than water and insoluble in water. The primary hazard is the threat to the environment. Immediate steps should be taken to limit spread to the environment. Toxic by ingestion. Used to make other chemicals.

공기와 물의 반응

Insoluble in water.

반응 프로필

Vigorous reactions, sometimes amounting to explosions, can result from the contact between aromatic hydrocarbons, such as Chrysene, and strong oxidizing agents. They can react exothermically with bases and with diazo compounds. Substitution at the benzene nucleus occurs by halogenation (acid catalyst), nitration, sulfonation, and the Friedel-Crafts reaction.

위험도

Possible carcinogen.

건강위험

There is very little information published onthe acute toxicity of chrysene. The oral toxicity is expected to be low. Animal studies showsufficient evidence of carcinogenicity. It produced skin cancer in animals. Subcutaneousadministration of chrysene in mice causedtumors at the site of application. Cancer-causing evidence in humans is not known. Ahistidine reversion–Ames test for mutagenicity showed positive.

화재위험

Some may burn but none ignite readily. Containers may explode when heated. Some may be transported hot.

Safety Profile

Confirmed carcinogen with experimental carcinogenic, neoplastigenic, and tumorigenic data by skin contact. Human mutation data reported. When heated to decomposition it emits acrid smoke and fumes.

잠재적 노출

Almost never found by itself, chrysene is found in gasoline and diesel exhaust as well as in cigarette smoke; and in coal tar; coal tar pitch; creosote. It is used in organic synthesis.

Carcinogenicity

The IARC has determined that there is limited evidence that chrysene is carcinogenic to experimental animals.ACGIH has classified chrysene as a confirmed animal carcinogen with unknown relevance to humans; a numerical threshold limit value (TLV) is not recommended.

환경귀착

Biological. When chrysene was statically incubated in the dark at 25 °C with yeast extract and settled domestic wastewater inoculum, significant biodegradation with varied adaptation rates was observed. At concentrations of 5 and 10 mg/L, 59 and 38% biodegradation, respectively, were observed after 28 d (Tabak et al., 1981).
Soil. The reported half-lives for chrysene in a Kidman sandy loam and McLaurin sandy loam are 371 and 387 d, respectively (Park et al., 1990).
Surface Water. In a 5-m deep surface water body, the calculated half-lives for direct photochemical transformation at 40 °N latitude, in the midsummer during midday were 13 h and 68 d with and without sediment-water partitioning, respectively (Zepp and Schlotzhauer, 1979).
Photolytic. Based on structurally related compounds, chrysene may undergo photolysis to yield quinones (U.S. EPA, 1985) and/or hydroxy derivatives (Nielsen et al., 1983). The atmospheric half-life was estimated to range from 0.802 to 8.02 h (Atkinson, 1987). Behymer and Hites (1985) determined the effect of different substrates on the rate of photooxidation of chrysene using a rotary photoreactor. The photolytic half-lives of chrysene using silica gel, alumina, and fly ash were 100, 78, and 38 h, respectively.

운송 방법

UN3077 Environmentally Hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required.

Purification Methods

Purify chrysene by chromatography on alumina from pet ether in a darkened room. Its solution in *C6H6 is passed through a column of decolorising charcoal, then crystallised by concentrating the eluate. It has also been purified by crystallising from *C6H6 or *C6H6/pet ether, and by zone refining. [Gorman et al. J Am Chem Soc 107 4404 1985]. It is freed from 5H-benzo[b]carbazole by dissolving it in N,N-dimethylformamide and successively adding small portions of alkali and iodomethane until the fluorescent colour of the carbazole anion no longer appears when alkali is added. The chrysene (and alkylated 5H-benzo[b]carbazole) separate on addition of water. Final purification is by crystallisation from ethylcyclohexane and/or from 2-methoxyethanol [Bender et al. Anal Chem 36 1011 1964]. It can be sublimed in a vacuum. [Beilstein 5 IV 2554.]

비 호환성

Contact with strong oxidizers may cause fire and explosion hazard

폐기물 처리

Chrysene may be destroyed by permanganate oxidation, by high-temperature incinerator with scrubbing equipment; or by microwave plasma treatment.

크리센 준비 용품 및 원자재

원자재

준비 용품


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