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2,3,6-Trimethylnaphthalene is a polycyclic aromatic hydrocarbon with the molecular formula C13H12. It is a derivative of naphthalene and has three methyl groups attached to different positions on the naphthalene ring.
Used in Chemical Industry:
2,3,6-Trimethylnaphthalene is used as a chemical intermediate for the production of dyes, pigments, and other organic compounds.
Used in Manufacturing Industry:
2,3,6-Trimethylnaphthalene is used as a solvent in the manufacturing of various products.
Used in Environmental Management:
2,3,6-Trimethylnaphthalene is classified as a hazardous substance and is handled and disposed of with caution to prevent harm to human health and the environment.

829-26-5

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829-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 829-26-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 829-26:
(5*8)+(4*2)+(3*9)+(2*2)+(1*6)=85
85 % 10 = 5
So 829-26-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H14/c1-9-4-5-12-7-10(2)11(3)8-13(12)6-9/h4-8H,1-3H3

829-26-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,6-TRIMETHYLNAPHTHALENE

1.2 Other means of identification

Product number -
Other names 2,3,6-Trimethylnaphthalin

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:829-26-5 SDS

829-26-5Relevant academic research and scientific papers

Benzannulation via ruthenium-catalyzed diol-diene [4+2] cycloaddition: One- and two-directional syntheses of fluoranthenes and acenes

Geary, Laina M.,Chen, Te-Yu,Montgomery, T. Patrick,Krische, Michael J.

supporting information, p. 5920 - 5922 (2014/05/20)

A new benzannulation protocol is described and applied to the synthesis of polycyclic aromatic hydrocarbons. Ruthenium(0)-catalyzed diol-diene [4+2] cycloaddition delivers cyclohex-1-ene-4,5-diols, which are subject to aromatization upon dehydration or Nicholas diol deoxydehydration. Employing diol and tetraol reactants, benzannulation can be conducted efficiently in one- and two-directional modes, respectively, as illustrated in the construction of substituted fluoranthenes and acenes.

Characterization of polycyclic aromatic hydrocarbon particulate and gaseous emissions from polystyrene combustion

Durlak, Susan K.,Biswas, Pratim,Shi, Jichun,Bernhard, Mary Jo

, p. 2301 - 2307 (2007/10/03)

The partitioning of polycyclic aromatic hydrocarbons (PAHs) between the particulate and gaseous phases resulting from the combustion of polystyrene was studied. A vertical tubular flow furnace was used to incinerate polystyrene spheres (100-300 μm) at different combustion temperatures (800- 1200 °C) to determine the effect of temperature and polystyrene feed size on the particulate and gaseous emissions and their chemical composition. The furnace reactor exhaust was sampled using real-time instruments (differential mobility particle sizer and/or optical particle counter) to determine the particle size distribution. For chemical composition analyses, the particles were either collected on Teflon filters or split into eight size fractions using a cascade impactor with filter media substrates, while the gaseous products were collected on XAD-2 adsorbent. Gas chromatography/mass spectroscopy (GC/MS) was used to identify and quantify the specific PAH species, their partitioning between the gas and particulate phases, and their distribution as a function of emission particle size. The total mass and number of PAH species in both the particulate and gas phases were found to decrease with increasing incineration temperature and decreasing polystyrene feed size, while the mean diameter of the particles increases with increasing incineration temperature and decreasing feed size. In addition, the PAH species in the particulate phase were found to be concentrated in the smaller aerosol sizes. The experimental results have been analyzed to elucidate the formation mechanisms of PAHs and particles during polystyrene combustion. The implications of these results are also discussed with respect to the control of PAH emissions from municipal waste-to-energy incineration systems. The partitioning of polycyclic aromatic hydrocarbons (PAHs) between particulate and gaseous phases resulting from the combustion of polystyrene was studied. A vertical tubular flow furnace was used to incinerate polystyrene spheres to determine the effect of temperature and polystyrene feed size on the particulate and gaseous emissions and their chemical composition. The furnace reactor exhaust was sampled using real-time instruments to determine the particle size distribution. The total mass and number of PAH species in both the particulate and gas phases were found to decrease with increasing incineration temperature and decreasing polystyrene feed size, while the mean diameter of the particles increases with increasing incineration temperature and decreasing feed size. In addition, the PAH species in the particulate phase were found to be concentrated in the smaller aerosol sizes.

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