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4-Methylpyrene is a polycyclic aromatic hydrocarbon (PAH) consisting of a fused ring structure of four benzene rings, with a methyl group attached to the fourth carbon atom. It is a colorless, crystalline solid with a molecular formula of C17H12 and a molecular weight of 216.28 g/mol. 4-METHYLPYRENE is formed during the incomplete combustion of organic materials, such as coal, wood, and tobacco, and is considered a potential environmental pollutant and carcinogen. Due to its lipophilic nature, 4-methylpyrene can accumulate in living organisms, posing risks to human health and the ecosystem.

3353-12-6

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3353-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3353-12-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,5 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3353-12:
(6*3)+(5*3)+(4*5)+(3*3)+(2*1)+(1*2)=66
66 % 10 = 6
So 3353-12-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H12/c1-11-10-14-6-2-4-12-8-9-13-5-3-7-15(11)17(13)16(12)14/h2-10H,1H3

3353-12-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-METHYLPYRENE

1.2 Other means of identification

Product number -
Other names Pyrene,4-methyl

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:3353-12-6 SDS

3353-12-6Relevant academic research and scientific papers

Characterization of the combustion products of polyethylene

Piao, Mingjun,Chu, Shaogang,Zheng, Minghui,Xu, Xiaobai

, p. 1497 - 1512 (2007/10/03)

Polyethylene (PE) was burned in a tube-type furnace with an air flow at a temperature of 600~900°C. Combustion products were collected with glass wool, glass fiber filter, and XAD-2 adsorbent. The analysis of the products was performed with GC-FID and GC-MSD. At low temperature, hydrocarbons were the major components, while at higher temperature the products were composed of polycyclic aromatic hydrocarbons. With the high performance of the Hewlett-Packard 6890GC-5973MSD, more compounds were identified in comparison with previous studies.

Convenient synthesis of cyclopentapyrene and 3,4-dihydrocyclopentapyrene. The reactivity of the pyrene dianion

Tintel, C.,Cornelisse, J.,Lugtenburg, J.

, p. 14 - 20 (2007/10/02)

The reactivity of the pyrene dianion has been investigated.Initial attack by electrophiles on the pyrene dianion has been shown to take place exclusively at the 4(9)-position, leading to monoanions (11,15) which can be converted into 9-substituted 1,9-dihydropyrene derivatives (12,16).The latter can be rearranged to give the novel 4-substituted 4,5-dihydropyrene derivatives (13,17), which provide access to 4-substituted pyrene derivatives (14,5).Cyclopentapyrene (1) and 3,4-dihydrocyclopentapyrene (2), two widespread environmental contaminants, have been synthesizedfrom pyrene in four (64percent) and in five (62percent), respectiveliy, utilizing the chemical properties of the pyrene dianion.In these easy and straightforward syntheses the thus far unknown 4,5-dihydro-4-pyreneacetic acid (17) plays a major role.

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