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(2'-methoxyvinyl)pyrene is a chemical compound derived from pyrene, a polycyclic aromatic hydrocarbon. It features a methoxy group and a vinyl group attached to the pyrene molecule, making it a known environmental pollutant with potential toxic effects on human health and the environment. This highly lipophilic chemical can bioaccumulate in living organisms, leading to long-term exposure and health risks, including its classification as a carcinogen due to its interaction with DNA and cellular components.

93265-41-9

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93265-41-9 Usage

Uses

Used in Environmental Monitoring and Research:
(2'-methoxyvinyl)pyrene is utilized as a marker for environmental pollution, particularly in studies assessing the presence and impact of polycyclic aromatic hydrocarbons in various ecosystems. Its detection helps in understanding the extent of contamination and the potential risks associated with exposure to such pollutants.
Used in Toxicology and Health Risk Assessment:
As a known carcinogen, (2'-methoxyvinyl)pyrene is used in toxicological research to study the mechanisms of carcinogenesis and the effects of exposure on human health. This aids in the development of guidelines and regulations for safe exposure levels and the management of environmental pollutants.
Used in Chemical Education and Training:
(2'-methoxyvinyl)pyrene serves as a case study in chemical education and training programs, highlighting the importance of understanding chemical properties, environmental impact, and safe handling procedures for hazardous substances.
Used in Development of Mitigation Strategies:
Understanding the properties and risks associated with (2'-methoxyvinyl)pyrene is crucial for the development of mitigation strategies to reduce its environmental impact and human exposure. This includes the design of effective waste management practices and the creation of policies to regulate the use and disposal of such chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 93265-41-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,6 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 93265-41:
(7*9)+(6*3)+(5*2)+(4*6)+(3*5)+(2*4)+(1*1)=139
139 % 10 = 9
So 93265-41-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H14O/c1-20-12-11-13-5-6-16-8-7-14-3-2-4-15-9-10-17(13)19(16)18(14)15/h2-12H,1H3/b12-11+

93265-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(E)-2-methoxyethenyl]pyrene

1.2 Other means of identification

Product number -
Other names trans-Mvp

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:93265-41-9 SDS

93265-41-9Downstream Products

93265-41-9Relevant academic research and scientific papers

Chemiluminescence Mechanism and Quantum Yield of Synthetic Vinylpyrene Analogues of Benzopyrene-7,8-dihydrodiol

Thompson, Ambler,Lever, John R.,Canella, Karen A.,Miura, Kyo,Posner, Gary H.,Seliger, H. H.

, p. 4498 - 4504 (2007/10/02)

We have previously reported that the dioxetane chemiluminescence (CL) of the proximate carcinogenic metabolite (+/-)-trans-7,8-dihydroxy-7,8-dihydrobenzopyrene (7,8-Diol) could be produced by free singlet oxygen (1O2) in solution.We now report that the trans-1-(2-methoxyvinyl)pyrene (t-MVP) model chemical analogue, in which an ene reaction is prevented, has a CL quantum yield ΦCL (t-MVP) of 0.0003, 180 times that of 7,8-diol.The CL emission spectrum of t-MVP was identical with the fluorescence emission spectrum of the dioxetane decomposition product, pyrene-1-carboxaldehyde (6 in Scheme II), which was isolated in 10 percent yield in 1O2 reactions.The solvent dependencies of ΦCL t-MVP of dioxetanes parallel the fluorescence quantum yield (ΦFluor) of 6 and the CL yield from dioxetanes of 7,8-Diol in these same solvents.This dioxetane CL of the t-MVP analogue supports the originally proposed dioxetane CL mechanism of 7,8-Diol.The limiting factor in 7,8-Diol CL appears to be the low chemical yield for formation of the 9,10-dioxetane.

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