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2,3,3-Trimethylhexane, with the molecular formula C9H20, is a branched-chain, saturated hydrocarbon belonging to the alkane family. This colorless liquid is insoluble in water and is recognized for its role as a solvent in various industrial applications.

16747-28-7

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16747-28-7 Usage

Uses

Used in the Petroleum Industry:
2,3,3-Trimethylhexane is used as a blending component in gasoline for the purpose of improving the octane rating. This enhancement helps in reducing the risk of engine knocking, which is crucial for the performance and longevity of internal combustion engines.
Used as a Starting Material in Chemical Production:
In the chemical industry, 2,3,3-Trimethylhexane serves as a starting material for the production of other chemicals. It is particularly utilized in the synthesis of polymers and surfactants, contributing to a wide range of applications across different sectors.
Safety Considerations:
Given its flammable nature, 2,3,3-Trimethylhexane should be handled with caution, ensuring it is used in a well-ventilated environment to minimize the risk of fire or explosion.

Check Digit Verification of cas no

The CAS Registry Mumber 16747-28-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,4 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16747-28:
(7*1)+(6*6)+(5*7)+(4*4)+(3*7)+(2*2)+(1*8)=127
127 % 10 = 7
So 16747-28-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H20/c1-6-7-9(4,5)8(2)3/h8H,6-7H2,1-5H3

16747-28-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,3-TRIMETHYLHEXANE

1.2 Other means of identification

Product number -
Other names EINECS 240-808-2

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:16747-28-7 SDS

16747-28-7Downstream Products

16747-28-7Relevant academic research and scientific papers

GAS-TO-GAS REACTOR AND METHOD OF USING

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Paragraph 0176-0178, (2021/02/05)

A device and a process to propagate molecular growth of hydrocarbons, either straight or branched chain structures, that naturally occur in the gas phase of a first gas to gas phase molecules of a second gas having higher molecular chain lengths than the hydrocarbons of the first gas. According to one embodiment, the device includes a grounded reactor vessel having a gas inlet, a product outlet, and an electrode within the vessel; a power supply coupled to the electrode for creating an electrostatic field within the vessel for converting the first gas to a second gas.

GAS-TO-LIQUID REACTOR AND METHOD OF USING

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Paragraph 0140-0142, (2019/08/15)

A device and a process to propagate molecular growth of hydrocarbons, either straight or branched chain structures, that naturally occur in the gas phase to a molecular size sufficient to shift the natural occurring phase to a liquid or solid state is provided. According to one embodiment, the device includes a grounded reactor vessel having a gas inlet, a liquid outlet, and an electrode within the vessel; a power supply coupled to the electrode for creating an elecirostatic field within the vessel for converting the gas to a liquid and or solid state.

Chemical transformations of isopentane and isooctane in trifluoromethanesulfonic acid

Gekhman,Smurnyi,Ustynyuk

, p. 1766 - 1770 (2007/10/03)

The process of isopentane and isooctane activation in trifluoromethanesulfonic acid (H0 = -14) has been studied by GC/MS and NMR. The results show evidence for a high reactivity of isopentane. Various mechanisms constructed using the experimental data and the results of nonempirical quantum-mechanical calculations are compared, and it is concluded that a key role in the reaction under consideration is played by the direct electrophilic attack of CF3SO3H at the C2-C3 bond of isooctane. Copyright

PRODUITS MOYENS DE LA RADIOLYSE DU DIMETHYL-2,3 BUTANE EN PHASE SOLIDE

Fontaine, L.M.,Claes, P.,Tilquin, B.

, p. 385 - 392 (2007/10/02)

2,3 Dimethylbutane was γ-irradiated in the quenched and annealed solid states at 77 K.G-yields of intermediate (C7 to C11) compounds were measured by gas chromatography.The alkene gases produced during radiolysis at 77 K may play a major role in the production of fragment alkyl or allyl radicals trapped during the radiolysis.By combination with the alkyl parent radical, these fragment radicals lead to intermediate compounds when the irradiated sample is warmed up.Post-irradiation scavenging of trapped radicals by dissolving the irradiated alkane in a propane-oxygen mixture lowered the intermediate product yield to an extend (47percent) corresponding to the radical contribution.

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