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3-(dibutoxymethyl)heptane is an organic compound with the molecular formula C15H32O2. It is a colorless liquid with a density of 0.84 g/cm3 and a boiling point of 288°C. This chemical is characterized by a heptane backbone with a methyl group at the third carbon position, which is further substituted by two butoxy groups. The compound is insoluble in water and has a low vapor pressure, making it suitable for use in various industrial applications, such as a solvent or a chemical intermediate. Due to its non-polar nature, it is also used in the extraction and purification of various organic compounds.

5460-40-2

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5460-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5460-40-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5460-40:
(6*5)+(5*4)+(4*6)+(3*0)+(2*4)+(1*0)=82
82 % 10 = 2
So 5460-40-2 is a valid CAS Registry Number.

5460-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(dibutoxymethyl)heptane

1.2 Other means of identification

Product number -
Other names 2-Aethyl-1,1-dibutoxy-hexan

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:5460-40-2 SDS

5460-40-2Downstream Products

5460-40-2Relevant academic research and scientific papers

Method for producing enol ethers

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, (2008/06/13)

Enol ethers of the formula I where R1is an aliphatic, cycloaliphatic, araliphatic, aromatic or heterocyclic radical which may carry further substituents which do not react with acetylenes or allenes, and the radicals R, independently of one another, are hydrogen or aliphatic, cycloaliphatic, araliphatic, aromatic or heterocyclic radicals, which may be bonded to one another to form a ring, and m is 0 or 1, are prepared by reacting an acetal or ketal of the formula II with an acetylene or allene of the formula III or IV where R and R1have the abovementioned meanings, in the gas phase at elevated temperatures in the presence of a zinc- or cadmium- and silicon- and oxygen-containing heterogeneous catalyst.

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