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54459-71-1

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54459-71-1 Usage

General Description

1-Butoxyhexane is a chemical compound composed of the 1-butoxy and hexane groups. It is commonly used as a solvent for various applications, including in the production of paints, coatings, and adhesives. This chemical is colorless and has a mild, sweet odor, making it suitable for use in consumer products. 1-Butoxyhexane is also known for its low volatility and low solubility in water, making it a stable and effective solvent for industrial processes. However, it is important to handle 1-butoxyhexane with care, as it can be harmful if ingested, inhaled, or absorbed through the skin. Proper safety precautions should be taken when working with this chemical to minimize potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 54459-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,5 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54459-71:
(7*5)+(6*4)+(5*4)+(4*5)+(3*9)+(2*7)+(1*1)=141
141 % 10 = 1
So 54459-71-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O/c1-3-5-7-8-10-11-9-6-4-2/h3-10H2,1-2H3

54459-71-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-butoxyhexane

1.2 Other means of identification

Product number -
Other names Hexane,1-butoxy

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:54459-71-1 SDS

54459-71-1Relevant articles and documents

Continuous-Flow Reductive Alkylation: Synthesis of Bio-based Symmetrical and Disymmetrical Ethers

Bruniaux, Sophie,Luart, Denis,Len, Christophe

, p. 1849 - 1856 (2018/02/06)

For the first time, a reductive alkylation process in continuous flow has been elaborated for the conversion of bio-based alcohols and aldehydes into symmetrical and dissymmetrical high-value-added ethers for industrial companies. The developed method is an etherification associating liquid, solid and gas phases under green conditions (continuous flow, catalysis, bio-based starting materials).

A rapid Williamson synthesis under microwave irradiation in dry medium

Bogdal, Dariusz,Pielichowski, Jan,Jaskot, Krzysztof

, p. 427 - 432 (2007/10/03)

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FLUORINATION OF 2-ALKYL-SUBSTITUTED OXIRANES. THE SYNTHESIS AND PURIFICATION OF PERFLUORO(2-ALKYL-SUBSTITUTED OXANE)S

Abe, Takashi,Hayashi, Eiji,Baba, Hajime,Kodaira, Kazuo,Nagase, Shunji

, p. 353 - 380 (2007/10/02)

Five kinds of 2-alkyl-substituted oxanes like 2-ethyloxane, 2-n-propyloxane, 2-iso-propyloxane, 2-n-butyloxane and 2-n-amyloxane were fluorinated electrochemically to give the corresponding perfluoro(2-alkyloxane)s.The perfluoro(2-alkyloxane)s were obtained in good yields from these starting materials together with isomeric perfluoro(2-alkyloxolane)s, perfluoro(2-alkyl-5-methyloxolane)s and perfluoro(dialkyl ether)s.The purification of the perfluoro(2-alkyloxane)s which contained small amounts of isomeric perfluoro(2-alkyloxolane)s was succesfully achieved by recovering the former unreacted after treating these mixtures with anhydrous aluminum chloride at 150-160 deg C during ca. 48 hrs in order to convert the latter into the easy-separable perfluoro-(2,5,5-trichloro-2-alkyloxolane)s.Small quantities of new perfluoro(5,5-dichloroalkanoyl chloride)s were also among the chlorination products.The spectroscopic data as well as the physical properties of these new fluorination products, and perfluoro(2,5,5-trichloro-2-alkyloxolane)s and perfluoro(5,5-dichloroalkanoyl chloride)s are presented.

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