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Decahydro-2,3-dimethylnaphthalene is a chemical compound with a unique structure consisting of ten hydrogen atoms and two carbon atoms, which contributes to its high stability and versatility in various applications. It is known for its aromatic properties and compatibility with other substances, making it a valuable component in different industries.

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  • 1008-80-6 Structure
  • Basic information

    1. Product Name: DECAHYDRO-2,3-DIMETHYLNAPHTHALENE
    2. Synonyms: DECAHYDRO-2,3-DIMETHYLNAPHTHALENE
    3. CAS NO:1008-80-6
    4. Molecular Formula: C12H22
    5. Molecular Weight: 166.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1008-80-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 218.3°Cat760mmHg
    3. Flash Point: 74.3°C
    4. Appearance: /
    5. Density: 0.838g/cm3
    6. Vapor Pressure: 0.187mmHg at 25°C
    7. Refractive Index: 1.452
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: DECAHYDRO-2,3-DIMETHYLNAPHTHALENE(CAS DataBase Reference)
    11. NIST Chemistry Reference: DECAHYDRO-2,3-DIMETHYLNAPHTHALENE(1008-80-6)
    12. EPA Substance Registry System: DECAHYDRO-2,3-DIMETHYLNAPHTHALENE(1008-80-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1008-80-6(Hazardous Substances Data)

1008-80-6 Usage

Uses

Used in Perfumery and Fragrance Industry:
Decahydro-2,3-dimethylnaphthalene is used as a key ingredient in the manufacture of perfumes and fragrances due to its aromatic properties. Its ability to blend well with various other substances enhances the overall scent profile and contributes to the creation of unique and appealing fragrances.
Used in Industrial Processes as a Solvent:
In the industrial sector, Decahydro-2,3-dimethylnaphthalene serves as a solvent due to its chemical stability and non-toxic nature. Its use in solvent applications allows for efficient and safe processing in various manufacturing and production activities, ensuring the quality and performance of the final products.

Check Digit Verification of cas no

The CAS Registry Mumber 1008-80-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1008-80:
(6*1)+(5*0)+(4*0)+(3*8)+(2*8)+(1*0)=46
46 % 10 = 6
So 1008-80-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H22/c1-9-7-11-5-3-4-6-12(11)8-10(9)2/h9-12H,3-8H2,1-2H3

1008-80-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dimethyl-1,2,3,4,4a,5,6,7,8,8a-decahydronaphthalene

1.2 Other means of identification

Product number -
Other names cis,trans,cis-3,4-Dimethyl-bicyclo<4.4.0>decan

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:1008-80-6 SDS

1008-80-6Upstream product

1008-80-6Downstream Products

1008-80-6Relevant articles and documents

Catalytic activity of in situ synthesized MoWNi sulfides in hydrogenation of aromatic hydrocarbons

Topolyuk, Yu. A.,Maksimov,Kolyagin, Yu. G.

, p. 205 - 212 (2017)

MoWNi–sulfide catalysts were obtained in situ by thermal decomposition of metal–polymer precursors based on the copolymers of polymaleic anhydride in a hydrocarbon raw material. The activity of the synthesized catalysts in hydrogenation of bicyclic aromatic hydrocarbons was studied, and the composition and structure of active phase nanoparticles were determined.

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