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2,4-dimethyl-3-hexene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 82085-14-1 Structure
  • Basic information

    1. Product Name: 2,4-dimethyl-3-hexene
    2. Synonyms: 2,4-dimethyl-3-hexene
    3. CAS NO:82085-14-1
    4. Molecular Formula:
    5. Molecular Weight: 112.215
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82085-14-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,4-dimethyl-3-hexene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-dimethyl-3-hexene(82085-14-1)
    11. EPA Substance Registry System: 2,4-dimethyl-3-hexene(82085-14-1)
  • 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: 82085-14-1(Hazardous Substances Data)

82085-14-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82085-14-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,8 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82085-14:
(7*8)+(6*2)+(5*0)+(4*8)+(3*5)+(2*1)+(1*4)=121
121 % 10 = 1
So 82085-14-1 is a valid CAS Registry Number.

82085-14-1Upstream product

82085-14-1Downstream Products

82085-14-1Relevant articles and documents

One-step hydroprocessing of fatty acids into renewable aromatic hydrocarbons over Ni/HZSM-5: Insights into the major reaction pathways

Xing, Shiyou,Lv, Pengmei,Wang, Jiayan,Fu, Junying,Fan, Pei,Yang, Lingmei,Yang, Gaixiu,Yuan, Zhenhong,Chen, Yong

, p. 2961 - 2973 (2017)

For high caloricity and stability in bio-aviation fuels, a certain content of aromatic hydrocarbons (AHCs, 8-25 wt%) is crucial. Fatty acids, obtained from waste or inedible oils, are a renewable and economic feedstock for AHC production. Considerable amounts of AHCs, up to 64.61 wt%, were produced through the one-step hydroprocessing of fatty acids over Ni/HZSM-5 catalysts. Hydrogenation, hydrocracking, and aromatization constituted the principal AHC formation processes. At a lower temperature, fatty acids were first hydrosaturated and then hydrodeoxygenated at metal sites to form long-chain hydrocarbons. Alternatively, the unsaturated fatty acids could be directly deoxygenated at acid sites without first being saturated. The long-chain hydrocarbons were cracked into gases such as ethane, propane, and C6-C8 olefins over the catalysts' Br?nsted acid sites; these underwent Diels-Alder reactions on the catalysts' Lewis acid sites to form AHCs. C6-C8 olefins were determined as critical intermediates for AHC formation. As the Ni content in the catalyst increased, the Br?nsted-acid site density was reduced due to coverage by the metal nanoparticles. Good performance was achieved with a loading of 10 wt% Ni, where the Ni nanoparticles exhibited a polyhedral morphology which exposed more active sites for aromatization.

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