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4-(Hexyloxy)-1-butanol, also known as 4-hexyloxybutan-1-ol, is a colorless liquid organic compound with the chemical formula C10H22O2. It is an ether derivative of 1-butanol, where a hydroxyl group is replaced by a hexyloxy group. 4-(HEXYLOXY)-1-BUTANOL is characterized by its molecular weight of 174.28 g/mol and a density of approximately 0.87 g/cm3. It is insoluble in water but soluble in most organic solvents. 4-(Hexyloxy)-1-butanol is used in the synthesis of various chemicals, pharmaceuticals, and as a solvent in industrial applications. It is also known for its potential use as a fragrance ingredient, adding a floral or fruity scent to perfumes and other products. Due to its chemical structure, it is considered less volatile and more stable than some other alcohols, which can be an advantage in certain applications.

4541-13-3

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4541-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4541-13-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,4 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4541-13:
(6*4)+(5*5)+(4*4)+(3*1)+(2*1)+(1*3)=73
73 % 10 = 3
So 4541-13-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H22O2/c1-2-3-4-6-9-12-10-7-5-8-11/h11H,2-10H2,1H3

4541-13-3SDS

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 4-hexoxybutan-1-ol

1.2 Other means of identification

Product number -
Other names 4-n-Hexoxy-1-butanol

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:4541-13-3 SDS

4541-13-3Downstream Products

4541-13-3Relevant academic research and scientific papers

Branch hydroxyoxaalkylmelamine chain and its use has compd.

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Paragraph 0116, (2018/07/28)

PROBLEM TO BE SOLVED: To provide a means capable of lowering the melting point or the glass transition point of a compound having straight chain alkyl chain or a compound having straight chain oxaalkyl chain and also lowering the viscosity including the kinematic viscosity or the like, and to provide a compound obtained by the means and a use of the compound. SOLUTION: The compound has an oxaalkyl chain which has at least one side chain, in a molecule. COPYRIGHT: (C)2012,JPOandINPIT

Synthesis and antiproliferative activity of alkylphosphocholines

Agresta, Mandy,D'Arrigo, Paola,Fasoli, Ezio,Losi, Daniele,Pedrocchi-Fantoni, Giuseppe,Riva, Simona,Servi, Stefano,Tessaro, Davide

, p. 201 - 210 (2007/10/03)

Alkylphosphocholines (APC) with one or more methylene groups in the alkyl chain replaced by oxygen atoms or carbonyl groups, or both have been assembled modularly using ω-diols as central building blocks. Out of 25 new compounds of this kind, 11 were evaluated for their antiproliferative activity on four cell lines and compared with miltefosine to evaluate their hemolytic activity (HA) and cytotoxicity on non-tumoral cells (MT2), used as markers of adverse effects. Compound 13 was more active on cancer cell lines than on non-tumoral cells and the data were similar for MTT and thymidine incorporation assays. It had less HA than miltefosine. Compound 13 could therefore be a candidate for the preparation of compounds with higher cytotoxicity on cancer cells and lower general toxicity.

Omega-hydrofluoroalkyl ethers, precursor carboxylic acids and derivatives thereof, and their preparation and application

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Page 17, (2010/01/31)

Normally liquid, omega-hydrofluoroalkyl ether compounds (and selected mixtures thereof) have a saturated perfluoroaliphatic chain of carbon atoms interrupted by one or more ether oxygen atoms. The compounds can be prepare, e.g. by decarboxylation of the corresponding fluoroalkyl ether carboxylic acids and are useful, e.g., in cleaning and drying applications.

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