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26094-13-3

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26094-13-3 Usage

Safety Profile

A skin and eye irritant. Whenheated to decomposition it emits toxic vapors of NOx.

Check Digit Verification of cas no

The CAS Registry Mumber 26094-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,9 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 26094-13:
(7*2)+(6*6)+(5*0)+(4*9)+(3*4)+(2*1)+(1*3)=103
103 % 10 = 3
So 26094-13-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H34O2.C4H11N/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20;1-2-3-4-5/h9-10H,2-8,11-17H2,1H3,(H,19,20);2-5H2,1H3/b10-9+;

26094-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-butylammonium oleate

1.2 Other means of identification

Product number -
Other names N-BUTYLAMINE OLEATE

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:26094-13-3 SDS

26094-13-3Downstream Products

26094-13-3Relevant articles and documents

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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