2,2,4-Trimethylheptane.

Base Information

• Chemical Name: 2,2,4-Trimethylheptane.
• CAS No.: 14720-74-2
• Molecular Formula: C10H22
• Molecular Weight: 142.285
• DSSTox Substance ID: DTXSID20871234
• Nikkaji Number: J110.594I
• Wikidata: Q5651159
• Mol file: 14720-74-2.mol

Synonyms:2,2,4-Trimethylheptane

Chemical Property of 2,2,4-Trimethylheptane.

Chemical Property:

• Vapor Pressure: 5.17mmHg at 25°C
• Melting Point: -53.99°C
• Refractive Index: 1.4069
• Boiling Point: 149.2°C at 760 mmHg
• Flash Point: 37.2°C
• PSA: 0.00000
• Density: 0.733g/cm³
• LogP: 3.85880
• XLogP3: 4.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 4
• Exact Mass: 142.172150702
• Heavy Atom Count: 10
• Complexity: 76.5

Purity/Quality:

99% ^*data from raw suppliers

2,2,4-Trimethylheptane ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Solvents -> Aliphatics, Saturated (
• Canonical SMILES: CCCC(C)CC(C)(C)C
• Uses: 2,2,4-Trimethylheptane is used as a component of jet fuels.

Technology Process of 2,2,4-Trimethylheptane.

There total 6 articles about 2,2,4-Trimethylheptane. which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

isobutene (115-11-7,15220-85-6) → 2,2,4-trimethylheptane (14720-74-2) + Permethyl 99A (13475-82-6)

Guidance literature:

With sulfuric acid; Hydrieren des Reaktionsgemisches in Gegenwart von Nickel bei 150grad und 16 at;

Reference yield:

1-butylene (106-98-9,9003-28-5) + (Z)-2-Butene (590-18-1) + trans-2-Butene (624-64-6) + Isobutane (75-28-5,40921-86-6) + 2,2-dimethylpropane (463-82-1) + methyl-cyclopentane (96-37-7) + n-butane (106-97-8,9003-29-6,9021-92-5) → 2,2,6-trimethyloctane (62016-28-8) + 2,4-dimethylpentane (108-08-7) + 2-Methylhexane (591-76-4) + 2,3,3-Trimethyl-pentane (560-21-4) + 2,3,4-trimethylpentane (565-75-3) + 2,2,4-trimethylpentane (540-84-1) + 2,5-dimethylhexane (592-13-2) + 2,3,4-trimethylhexane (921-47-1) + heptane, 3,3,5-trimethyl- (7154-80-5) + 2,3,5-trimethylheptane (20278-85-7) + 2,3,6-trimethylheptane (4032-93-3) + 2,2,4-trimethylheptane (14720-74-2) + 2,3-dimethyl pentane (565-59-3) + 2,3-dimethylhexane (584-94-1,116724-01-7) + 2,4-dimethylhexane (589-43-5) + methylbutane (78-78-4) + 3-methylpentane (96-14-0) + 2-Methylpentane (107-83-5) + 2,3-dimethylbutane (79-29-8) + triptane (464-06-2) + 2,4-dimethylheptane (2213-23-2) + 2,6-dimethylheptane (1072-05-5) + 2,2,5-trimethylhexane (3522-94-9) + cyclohexane (110-82-7,25012-93-5)

Guidance literature:

sulfuric acid; In water; at 1.65666 ℃; under 2963.34 Torr; Product distribution / selectivity;

Reference yield:

2,2,4-trimethyl-heptan-4-ol (57233-31-5) → 2,2,4-trimethylheptane (14720-74-2)

Guidance literature:

With CuSO₄-pumice stone; at 200 ℃; under 200 Torr; Hydrieren des erhaltenen Olefingemisches an Nickel-Kieselgur bei 110-130grad und 84 at;

upstream raw materials:

2,2,4-trimethyl-heptan-4-ol

isobutene

propene

Isobutane

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