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Octanoic acid, compd. with 1-butanamine (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17463-28-4

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17463-28-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17463-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,6 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17463-28:
(7*1)+(6*7)+(5*4)+(4*6)+(3*3)+(2*2)+(1*8)=114
114 % 10 = 4
So 17463-28-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O2.C4H11N/c1-2-3-4-5-6-7-8(9)10;1-2-3-4-5/h2-7H2,1H3,(H,9,10);2-5H2,1H3

17463-28-4SDS

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 butan-1-amine,octanoic acid

1.2 Other means of identification

Product number -
Other names butylammonium octanoate

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:17463-28-4 SDS

17463-28-4Downstream Products

17463-28-4Relevant academic research and scientific papers

Synthesis and characterization of new low-cost ILs based on butylammonium cation and application to lignocellulose hydrolysis

De Andrade Neto, José Carlos,De Souza Cabral, Allex,De Oliveira, Lucas Rissato Dognani,Torres, Ricardo Belchior,Morandim-Giannetti, Andreia De Araújo

, p. 279 - 287 (2016/03/01)

Fourteen ionic liquids (ILs) were obtained and characterized by nuclear magnetic resonance and infra-red spectroscopy. One of these liquids, n-butylammonium acetate, was used in the treatment of coir fiber prior to acid hydrolysis. For this purpose, the fiber was pulped with 8% (w/w) sodium hydroxide for 6 h under 2.5 atm pressure at 137 °C and then treated with IL for 2 h at 90 °C. The samples were hydrolyzed in acetic acid at different concentrations and temperatures. The reducing sugar concentrations were determined in all samples, and the optimal hydrolysis conditions were established (32.2% acetic acid at 122.4 °C). The reaction time was also studied, and the conversion was maximized at 3 h. Under the best hydrolysis conditions, crude fiber, pulping fiber, and IL-treated fiber were hydrolyzed to yield 8.53%, 47.58%, and 89.75% of reducing sugars, respectively.

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