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오발렌

Ovalene

HCID 67446
노트반응
기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
190-26-1
표준 SMILES
c1cc2ccc3cc4ccc5ccc6ccc7cc8ccc1c1c2c3c2c4c5c6c7c2c81
InChIKey
LSQODMMMSXHVCN-UHFFFAOYSA-N
분자식
C32H14
평균 분자량
398.5 g/mol
단동위원소 질량
398.10955045

개요

Ovalene is an ortho- and peri-fused polycyclic arene.

이름 및 식별자

우선 이름
Ovalene
IUPAC
ovalene
현지명
오발렌
영어명
Ovalene
분자식
C32H14
분자량
398.45

이름 및 동의어

Ovalene190-26-1UNII-3M1901484GEINECS 205-880-1NSC 91578NSC-915783M1901484GCHEBI:33091DTXSID901724471,14:3,4:7,8:10,11-Tetraethenodibenzo[fg,op]naphthacene1,14:3,4:7,8:10,11-Tetraethenodibenzo(fg,op)naphthaceneRefChem:168734
이름 더 보기
오발렌
DTXCID6094938205-880-1LSQODMMMSXHVCN-UHFFFAOYSA-NSCHEMBL27402SCHEMBL22344177SCHEMBL29354165NSC91578phenanthro[3,4,5,6-qrabc]coronene

데이터베이스 식별자

CAS
190-26-1
PubChem CID
67446
DTXSID
DTXSID90172447
ChEBI
CHEBI:33091
UNII
3M1901484G
EC Number
205-880-1
Nikkaji
J145.956B

물성

구조 계산 물성

XLogP
10
극성 표면적
0 Ų
수소 결합 공여자 수
0
수소 결합 수용자 수
0
회전 가능 결합 수
0
무거운 원자 수
32
형식 전하
0
복잡도
696

실험 및 물리화학적 성질

SpringerMaterials PropertiesAngular frequency

물리화학적 성질

녹는점
475 · 475-476 °C
끓는 점
456.64 °C · 456.64°C (rough estimate)
밀도
0.853 · 0.8530 (rough estimate)
굴절률
1.469 · 1.4690 (estimate)

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

독성 정보

TreatmentThere is no know antidote for PAHs. Exposure is usually handled with symptomatic treatment. (L10)
Health EffectsPAHs are carcinogens and have been associated with the increased risk of skin, respiratory tract, bladder, stomach, and kidney cancers. They may also cause reproductive effects and depress the immune system. (L10)
Exposure RoutesOral (L10) ; inhalation (L10)
Toxicity Summary · 1건

The ability of PAH's to bind to blood proteins such as albumin allows them to be transported throughout the body. Many PAH's induce the expression of cytochrome P450 enzymes, especially CYP1A1, CYP1A2, and CYP1B1, by binding to the aryl hydrocarbon receptor or glycine N-methyltransferase protein. These enzymes metabolize PAH's into their toxic intermediates. The reactive metabolites of PAHs (epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations) covalently bind to DNA and other cellular macromolecules, initiating mutagenesis and carcinogenesis. (L10, L23, A27, A32)

Signs and SymptomsAcute exposure to PAHs causes irritation and inflammation of the skin and lung tissue. (A10)
Carcinogen ClassificationNot listed by IARC. IARC has evaluated other PAHs (L2154).

화학 및 산업

약리 정보

Metabolism/Metabolites · 1건

PAH metabolism occurs in all tissues, usually by cytochrome P-450 and its associated enzymes. PAHs are metabolized into reactive intermediates, which include epoxide intermediates, dihydrodiols, phenols, quinones, and their various combinations. The phenols, quinones, and dihydrodiols can all be conjugated to glucuronides and sulfate esters; the quinones also form glutathione conjugates. (L10)

용도 및 제조

Uses · 1건

PAHs are released into the environment via the combustion of fossil fuels, coke oven emissions and vehicle exhausts, as well as naturally from forest fires and vocanic eruptions. PAHs from these sources may contaminate nearly water systems. They are also found in coal tar and charbroiled food. (L10)

응용 분야

용도Ovalene can be used in technical or engineered material use in polymeric nanotube dispersants and dispersant-free nanotube films therefrom.

상·하류 제품 정보

하류 제품

2,3,6,7-테트라클로로나프탈렌1,4,6-트리클로로나프탈렌1,2,3,6,8-펜타클로로나프탈렌

공급사8 곳

江苏智芯廷科技有限公司18221391031 · [email protected]

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