Welcome to LookChem.com Sign In|Join Free
  • or
2-HYDROXY-5-NONYL-BENZALDEHYDE OXIME is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50849-47-3

Post Buying Request

50849-47-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

50849-47-3 Usage

Chemical Properties

Brown viscous liquid

Synthesis Reference(s)

Tetrahedron Letters, 35, p. 2393, 1994 DOI: 10.1016/0040-4039(94)85228-6

Check Digit Verification of cas no

The CAS Registry Mumber 50849-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,4 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 50849-47:
(7*5)+(6*0)+(5*8)+(4*4)+(3*9)+(2*4)+(1*7)=133
133 % 10 = 3
So 50849-47-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H25NO2/c1-2-3-4-5-6-7-8-9-14-10-11-16(18)15(12-14)13-17-19/h10-13,18-19H,2-9H2,1H3/b17-13+

50849-47-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Hydroxy-5-nonyl-benzaldehyde oxime

1.2 Other means of identification

Product number -
Other names acorgap50

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Processing aids, not otherwise listed
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:50849-47-3 SDS

50849-47-3Downstream Products

50849-47-3Relevant academic research and scientific papers

Characterization of 5-nonylsalicylaldoxime production and the effects of modifiers on its extracting/stripping properties

Pouramini, Zeinab,Moradi, Ali

, p. 2401 - 2409 (2012)

The 5-nonylsalicylaldoxime or 2-hydroxy-5-nonylbenzaldoxime namely aldoxime is a strong copper extractor that is mainly used in the process of copper solvent extractions. In order to characterize the aldoxime production process and to obtain a pure substance for using in the subsequent investigations, this reagent was synthesized and instrumental analysis such as FT-IR, 1H-NMR, and GC/MS spectra were first taken on the final product. The effects of various modifying reagents were studied on the synthesized aldoxime for improving its extracting and striping properties in the Cu (II) extraction processes. An optimum formulation of organic phase including the aldoxime and some modifier reagents was determined based on the variation of type and the concentration of the modifiers. The obtained experimental data show that the net copper transferring in a mixture of the aldoxime and modifier mainly the aliphatic alcohols (C12 (40 % w/w) and C14 (60 % w/w)) is greater than the aldoxime alone and greater than its other mixture. Springer Science+Business Media B.V. 2012.

A METHOD FOR THE PREPARATION OF ALKYLSALICYLALDEHYDE AND ALKYLSALICYLALDOXIME, AND USE THEREOF

-

Page/Page column 16-17, (2017/02/09)

The invention relates to an improved method for the preparation of alkylsalicylaldehyde or its corresponding metallic salts. The invention also relates to a method for the preparation of alkylsalicylaldoxime by reacting said alkylsalicylaldehyde or its corresponding metallic salts with hydroxylamine or its salt. The invention also relates to a method for extracting a metal in an aqueous solution containing dissolved metal.

METHOD FOR PREPARATION OF 5-ALKYLSALICYLALDOXIMES AND APPLICATION THEREOF

-

Paragraph 0019-0023, (2018/01/18)

Method for preparation of 5-alkylsalicylaldoximes with formula 1, where R is a C6-C16 alkyl group, consisting in that into a water-alcohol solvent system, p-alkylphenol, sodium hydroxide, chloroform and hydroxylamine are introduced, while in relation to the alkylphenol used, sodium hydroxide and chloroform are used in amounts from the stoichiometric amount to a 100% excess, and hydroxylamine is used in amounts from the stoichiometric amount to a 60% excess, and the reaction is carried out at a temperature of 60-75° C. for 1.5-4 h, and then, at a temperature of 20-30° C., the post-reaction mixture is acidified till the pH of the aqueous phase a neutral C5-C10 hydrocarbon solvent, the layers are separated, and the solvent is distilled off from the organic phase.

Comparing of 5-nonylsalicylaldoxime and salicylaldehyde characterization using magnesium salt formylation process

Pouramini, Zeinab,Moradi, Ali

experimental part, p. 357 - 362 (2012/09/08)

5-Nonylsalicylaldoxime and salicylaldehyde are two derivatives of phenolic compounds which are very applicable materials in industries. Formerly the formylation of phenolic derivatives were carried out by Rimer-Tiemann method. In this work both of these two materials were synthesized by magnesium meditated formylation technique and their structural characterizations were compared by instrumental analysis technique. In order to achieve a selectively orthoformylated product, the hydroxyl group of nonylphenol (or phenol) was first modified by magnesium methoxide. The nonylphenol magnesium salt was then formylated by paraformaldehyde. The oximation reaction was finally applied to the prepared non-ylsalicylaldehyde magnesium salt by liquid extracting via water and acid washing and other extractions. The solvent was finally removed by evaporation under reduced pressure. Some instrumental analysis such as 1H-NMR, GC/MS and FT-IR spectra were taken on the product in order to interpret the reaction characterization quantitatively and qualitatively. The formaldehyde and oxime functional groups of two compounds were investigated through 1H-NMR and FT-IR spectra and were compared. The yield of methoxilation was very good and the yields of formylation and oximation reactions were about 90%and 85% respectively. The orthoselectivity of formylation reaction were evaluated by comparing of the relevant spectra. The GC/MS spectra also confirmed the obtained results.

A NOVEL PROCESS FOR THE MANUFACTURE OF 5-NONYL SALICYLALDOXIME

-

Page/Page column 7-9, (2010/11/26)

The invention relates to a process for producing 5-nonyl salicylaldoxime that comprises of converting nonyl phenol to a 5-nonyl aldehyde in a two-step reaction using a novel catalyst mixture, followed by the oximation of the said aldehyde using hydroxylamine sulphate, and that the said catalytic process of aldehyde production is the main invention, in that the effective use of the catalyst mixture helps the reaction proceed at a faster and controlled rate which leads to a higher yield of aldehyde, as a result of complete conversion of all the reactants to the final products.

Reaction of nitromethane with aluminium phenolates: Mild synthesis of salicylaldoximes

Sartori, Giovanni,Bigi, Franca,Maggi, Raimondo,Tomasini, Fabio

, p. 2393 - 2396 (2007/10/02)

A mild synthesis of phenolic oximes has been performed by heating AlCl3 in nitromethane with suitable phenols (molar ratio 2:1).

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 50849-47-3