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2591-79-9

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2591-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2591-79-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2591-79:
(6*2)+(5*5)+(4*9)+(3*1)+(2*7)+(1*9)=99
99 % 10 = 9
So 2591-79-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H13NO/c1-2-3-4-5-7-6-8/h6H,2-5H2,1H3,(H,7,8)

2591-79-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-pentylformamide

1.2 Other means of identification

Product number -
Other names Formyl-pentylamin

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:2591-79-9 SDS

2591-79-9Relevant articles and documents

Electro-Fenton treatment of imidazolium-based ionic liquids: Kinetics and degradation pathways

Bocos, Elvira,Pazos, Marta,Sanromán, M. ángeles

, p. 1958 - 1965 (2016/01/20)

In this study, the removal of five imidazolium-based ionic liquids (ILs) from water was accomplished by a heterogeneous electro-Fenton treatment. Different ILs were selected in order to study the effect of the alkyl chain length and the nature of the anion. Initially, the effect of the catalyst (iron alginate beads) dosage and current were evaluated. The results showed that the optimum conditions were attained when operating with 4.27 g of catalyst and 0.3 A, achieving degradation yields and TOC reductions higher than 95% after 90 min and 80% after 480 min, respectively. Regarding the ILs with common cations, lower degradation rates were obtained for those with longer alkyl chains, thus 1-ethyl-3-methylimidazolium dicyanamide, exhibits faster degradation than 1-hexyl-3-methylimidazolium dicyanamide and 1-butyl-3-methylimidazolium dicyanamide. In addition, the influence of the counter anions on the oxidation rate of different ILs under an electro-Fenton treatment was demonstrated, following the order: methylsulfate > dicyanamide > acetate. The Microtox ecotoxicity tests of the initial and treated samples revealed that none of the three studied ILs with shorter alkyl chain lengths showed toxicity and only 1-hexyl-3-methylimidazolium dicyanamide and 1-butyl-3-methylimidazolium dicyanamide presented toxic levels, with EC50 values of 269.85 and 47.55 mg L-1, respectively. Nonetheless, after 480 min of heterogeneous electro-Fenton treatment at 0.3 A, the toxicity of both was completely reduced. Finally, to confirm the mineralization of these compounds, the identification of several reaction intermediates in the heterogeneous electro-Fenton treatment of three ILs was assayed and a plausible degradation pathway was proposed.

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