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218-01-9

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218-01-9 Usage

Description

Chrysene is a polycyclic aromatic hydrocarbon (PAH) composed of four fused benzene rings. It is a prevalent environmental contaminant that arises from the incomplete combustion of organic materials such as coal, oil, and gas. Classified as a Group 2B carcinogen by the International Agency for Research on Cancer (IARC), chrysene is recognized for its potential to pose a significant health risk to humans. Its capacity to accumulate in the environment and food chain makes it a concern for human exposure, which can occur through various routes including inhalation of contaminated air, ingestion of contaminated food and water, and dermal absorption.

Uses

Given the provided materials, there are no direct applications of chrysene mentioned, as it is primarily recognized for its harmful effects and efforts are focused on reducing its presence in the environment to mitigate health risks. However, in a broader context, understanding chrysene's properties and its environmental behavior is crucial for:
1. Environmental Monitoring and Remediation:
Chrysene is used as a target pollutant for monitoring the presence of PAHs in environmental samples. This helps in assessing the level of contamination and implementing appropriate remediation strategies to reduce exposure and mitigate health risks.
2. Research and Development:
Chrysene serves as a subject of study in research aimed at understanding the mechanisms of carcinogenesis and developing methods for the detection, prevention, and treatment of PAH-induced health issues. This includes exploring ways to degrade or sequester chrysene in the environment and developing personal protective measures against exposure.
3. Regulatory Frameworks:
Chrysene is used as a reference compound in setting regulatory standards and guidelines for permissible levels of PAHs in air, water, soil, and food products. This aids in the enforcement of environmental and public health protection policies.
4. Industrial Safety Measures:
In industries where incomplete combustion of organic materials is a part of the process, chrysene is considered when designing safety measures and emission control technologies to minimize the release of PAHs, including chrysene, into the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 218-01-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,1 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 218-01:
(5*2)+(4*1)+(3*8)+(2*0)+(1*1)=39
39 % 10 = 9
So 218-01-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H12/c1-3-7-15-13(5-1)9-11-18-16-8-4-2-6-14(16)10-12-17(15)18/h1-12H

218-01-9 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • Supelco

  • (40074)  Chrysenesolution  certified reference material, 1000 μg/mL in acetone

  • 218-01-9

  • 000000000000040074

  • 359.19CNY

  • Detail
  • Sigma-Aldrich

  • (94035)  Chrysene  certified reference material, TraceCERT®

  • 218-01-9

  • 94035-50MG

  • 1,096.29CNY

  • Detail
  • Sigma-Aldrich

  • (35754)  Chrysene  analytical standard

  • 218-01-9

  • 35754-100MG

  • 1,100.97CNY

  • Detail
  • Sigma-Aldrich

  • (BCR269)  Chrysene  BCR® certified Reference Material

  • 218-01-9

  • BCR269-20MG

  • 3,333.33CNY

  • Detail
  • Supelco

  • (48565-U)  Chrysene  analytical standard

  • 218-01-9

  • 48565-U

  • 492.57CNY

  • Detail
  • Supelco

  • (CRM48650)  Chrysene Solution  200 μg/mL in methylene chloride, certified reference material, TraceCERT®, ampule of 1 mL

  • 218-01-9

  • CRM48650

  • 300.69CNY

  • Detail
  • Aldrich

  • (769215)  Chrysene  

  • 218-01-9

  • 769215-500MG

  • 1,862.64CNY

  • Detail
  • Aldrich

  • (769215)  Chrysene  

  • 218-01-9

  • 769215-1G

  • 3,105.18CNY

  • Detail

218-01-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name chrysene

1.2 Other means of identification

Product number -
Other names 1,2,5,6-Dibenzonaphthalene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:218-01-9 SDS

218-01-9Related news

Biodegradation of dibenzothiophene, fluoranthene, pyrene and Chrysene (cas 218-01-9) in a soil slurry reactor by the white-rot fungus Bjerkandera sp. BOS5509/30/2019

Mass transfer phenomena can be an important constraint of the soil remediation process. With the goal of minimizing the mass transfer limitation, the degradation of four different PAHs by the white-rot fungus Bjerkandera adusta in a spiked marsh soil was evaluated in a slurry system. Key factors...detailed

A Naphtho‐Fused Double [7]Helicene from a Maleate‐Bridged Chrysene (cas 218-01-9) Trimer09/29/2019

Perkin condensation of chrysenyl‐6‐acetic acid with chrysenylene‐6,12‐diglyoxylic acid followed by in situ esterification gives a bismaleate, whose conjugated stilbene moieties are efficiently shielded against intermolecular condensations and undergo iodine‐catalyzed oxidative photocyclizat...detailed

From Chrysene (cas 218-01-9) to Double [5]Helicenes09/28/2019

Glyoxylic functionalization of chrysene by Friedel–Crafts acylation with ethyl chloroglyoxylate or by bromination followed by substituent exchange enables the formation of bis[5]helicene‐tetracarboxylates and tetracarboxdiimides through Perkin reactions and palladium‐catalyzed cyclizations. T...detailed

218-01-9Relevant articles and documents

Peak,Robinson

, (1937)

Raudnitz,Petru,Haurowitz

, p. 103,106 (1932)

Dansi,Salvioni

, p. 549,550 (1941)

-

Ruzicka et al.

, p. 833,839 (1933)

-

-

Diels,Gaedke

, (1927)

-

Cantoni et al.

, p. 1374 (1954)

Alumina-Mediated π-Activation of Alkynes

Akhmetov, Vladimir,Amsharov, Konstantin,Feofanov, Mikhail,Sharapa, Dmitry I.

supporting information, p. 15420 - 15426 (2021/09/30)

The ability to induce powerful atom-economic transformation of alkynes is the key feature of carbophilic π-Lewis acids such as gold- and platinum-based catalysts. The unique catalytic activity of these compounds in electrophilic activations of alkynes is explained through relativistic effects, enabling efficient orbital overlapping with π-systems. For this reason, it is believed that noble metals are indispensable components in the catalysis of such reactions. In this study, we report that thermally activated γ-Al2O3activates enynes, diynes, and arene-ynes in a manner enabling reactions that were typically assigned to the softest π-Lewis acids, while some were known to be triggered exclusively by gold catalysts. We demonstrate the scope of these transformations and suggest a qualitative explanation of this phenomenon based on the Dewar-Chatt-Duncanson model confirmed by density functional theory calculations.

Construction of Phenanthrenes and Chrysenes from β-Bromovinylarenes via Aryne Diels-Alder Reaction/Aromatization

Singh, Vikram,Verma, Ram Subhawan,Khatana, Anil K.,Tiwari, Bhoopendra

, p. 14161 - 14167 (2019/10/28)

A highly efficient transition-metal-free general method for the synthesis of polycyclic aromatic hydrocarbons like phenanthrenes and chrysenes (and tetraphene) from β-bromovinylarenes and arynes has been developed. The reactions proceed via an aryne Diels-Alder (ADA) reaction, followed by a facile aromatization. This is the first report on direct construction of chrysenes (and tetraphene) using the ADA approach. Unlike the literature method which is limited to only 9/10-substituted derivatives, this method gives access to a wide variety of functionalized phenanthrenes.

Oxidative, Iodoarene-Catalyzed Intramolecular Alkene Arylation for the Synthesis of Polycyclic Aromatic Hydrocarbons

Zhao, Zhensheng,Britt, Liam H.,Murphy, Graham K.

, p. 17002 - 17005 (2018/11/01)

A catalytic, metal-free and chemoselective oxidative intramolecular coupling of arene and alkene C?H bonds is reported. The active hypervalent iodine (HVI) reagent, generated catalytically in situ from iodotoluene and meta-chloroperoxybenzoic acid (m-CPBA), reacts with o-vinylbiphenyls to generate polyaromatic hydrocarbons in up to 95 % yield. Experimental evidence suggests the reactions proceed though vinyliodonium and, possibly, vinylenephenonium intermediates.

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