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N-Propyl pelargonate, also known as 2-ethylhexyl pelargonate or octanoic acid, 2-ethylhexyl ester, is a colorless liquid chemical compound with the molecular formula C11H22O2. It is an ester derived from the reaction of n-propyl alcohol and pelargonic acid, which is a saturated monocarboxylic acid with an 8-carbon chain. N-Propyl pelargonate is commonly used as a solvent, plasticizer, and fragrance ingredient in various industrial applications, including the production of adhesives, sealants, and cosmetics. It is also known for its ability to dissolve certain types of polymers and resins, making it a valuable component in the formulation of various products. Due to its potential health and environmental concerns, it is important to handle n-propyl pelargonate with care and adhere to proper safety guidelines.

6513-03-7

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6513-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6513-03-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,1 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6513-03:
(6*6)+(5*5)+(4*1)+(3*3)+(2*0)+(1*3)=77
77 % 10 = 7
So 6513-03-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H24O2/c1-3-5-6-7-8-9-10-12(13)14-11-4-2/h3-11H2,1-2H3

6513-03-7SDS

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 propyl nonanoate

1.2 Other means of identification

Product number -
Other names Propyl nonan-1-oate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:6513-03-7 SDS

6513-03-7Relevant academic research and scientific papers

Polymer-supported sulfonated magnetic resin: An efficient reagent for esterification of O-alkyl alkylphosphonic-and carboxylic-acids

Purohit, Ajay Kumar,Kumar, Ajeet,Singh, Varoon,Goud D, Raghavender,Jain, Rajiv,Dubey

supporting information, p. 6844 - 6846 (2015/01/09)

A mild and efficient synthetic method has been developed for the esterification of O-alkyl alkylphosphonic-and carboxylic-acids using polymer-supported sulfonated magnetic resins. Polymer-supported resins are recovered using an external magnet and reused several times.

Reductive cleavage versus hydrogenation of allyl aryl ethers and allylic esters using sodium borohydride/catalytic ruthenium(III) in various aqueous solvent mixtures

Babler, James H.,White, Nicholas A.,Kowalski, Eric,Jast, Jeffrey R.

experimental part, p. 745 - 748 (2011/03/21)

The reduction of allyl aryl ethers using sodium borohydride in the presence of a catalytic amount of ruthenium(III) chloride in various aqueous solvent mixtures at 0 °C was examined. In aqueous tetrahydrofuran, hydrogenation was the favored pathway (85-100% yield of the corresponding aryl propyl ether); whereas in aqueous N-methylformamide, reductive cleavage predominated (4:1 mixture of phenolic product/aryl propyl ether). In order to gain some insight into the mechanism for this process, 3-octyn-1-ol and trans-2-decen-1-yl acetate were subjected to similar reductive conditions; and both substrates afforded products inconsistent with a single-electron-transfer mechanism.

Regiochemical control in palladium(0) and palladium(II) catalysed alkene-formate ester carbonylation reactions

Lin, Ivan J. B.,Alper, Howard

, p. 248 - 249 (2007/10/02)

Palladium(0) complexes [Pd(PPh3)4 or Pd(dba) 2], (dba = dibenzylideneacetone) in the presence of 1,4-bis(diphenylphosphino)butane, can catalyse the reaction of alkenes and formate esters to give linear carboxylic esters as the major product, while the branched chain isomer was the principal ester obtained by use of a palladium(II) complex [bis(triphenylphosphine)palladium dichloride] as the catalyst.

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