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Nonane, 4-ethyl-5-methyl-, also known as 4-ethyl-5-methylnonane or 4,5-dimethyl-4-ethylnonane, is a branched-chain alkane with the molecular formula C11H24. It is a colorless, flammable liquid with a density of approximately 0.73 g/cm3 and a boiling point of around 171°C. This organic compound is a member of the alkane family, which consists of hydrocarbons with single bonds between carbon atoms. Nonane, 4-ethyl-5-methyl-, is primarily used as a solvent, a chemical intermediate, and in the production of various chemicals and fuels. Due to its low toxicity and relatively stable nature, it is considered a safer alternative to some other alkanes. However, it is still important to handle Nonane, 4-ethyl-5-methyl- with care, as inhalation or skin contact can cause irritation or other adverse effects.

1632-71-9

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1632-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1632-71-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,3 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1632-71:
(6*1)+(5*6)+(4*3)+(3*2)+(2*7)+(1*1)=69
69 % 10 = 9
So 1632-71-9 is a valid CAS Registry Number.

1632-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethyl-5-methylnonane

1.2 Other means of identification

Product number -
Other names 4-ethyl-5-methyl-nonane

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:1632-71-9 SDS

1632-71-9Upstream product

1632-71-9Downstream Products

1632-71-9Relevant academic research and scientific papers

RADIATION CHEMISTRY OF N-HEXANE AQUEOUS SOLUTIONS AS STUDIED BY CHROMATOGRAPHIC ANALYSIS OF FINAL PRODUCTS

Doncker, J. de,Tilquin, B.

, p. 107 - 113 (2007/10/02)

Radiolysis of dilute oxygen-free hexane aqueous solutions give dodecanes isomers analyzed by capillary gas chromatography.The relative yields for radicals which react by radical-radical recombination reactions are 39 percent, 32 percent and 29 percent for primary hexyl radical, secondary-2 hexyl radical and secondary-3 hexyl radical respectively.This distribution is changed with the N2O saturation before the radiolysis to 22 percent, 42 percent and 37 percent.If the first distribution is statistic, the increase of OH. available to attack the solute gives the distribution existing in pure alkane radiolysis.

Radiolyse des alcanes en phase liquide: nouvelles evidences experimentales et nouveau schema radiolytique

Tilquin, B.,Doncker, J. de

, p. 1195 - 1208 (2007/10/02)

Yields of final products (dimers) from the radiolysis of n-hexane and 2,3-dimethylbutane are studied by capillary chromatographic techniques for trace analysis.Reaction of intermediates with the products, the alkane molecules or impurities, is reduced by using low dose (1 kGy), low temperature (195 K) and high dose rate (LINAC).Temperature is the most important experiment variable; by reducing the temperature, reactions with sgnificant activation energies do not compete with radical-radical termination reactions.Products from LINAC radiolysis provide information about active species (reactive fragment, allylic radical...) which deserve a more detailed examination by direct methods.

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