77635-32-6 Usage
General Description
5-dodecyl-2-hydroxybenzaldehyde oxime is a chemical compound used as a chelating agent and extractant in the hydrometallurgical process of metal extraction. It is an organic compound with a dodecyl group attached to a hydroxybenzaldehyde oxime molecule, giving it the capacity to form stable complexes with metal ions. 5-dodecyl-2-hydroxybenzaldehyde oxime is commonly utilized in the recovery and separation of metal ions, particularly copper and nickel, from aqueous solutions. Its chelating properties make it suitable for various industrial applications, such as in mining and metallurgy, as well as in the production of organic coatings and adhesives. Additionally, 5-dodecyl-2-hydroxybenzaldehyde oxime has potential applications in the pharmaceutical and agricultural industries for its ability to bind to metal ions and facilitate their removal or utilization.
Check Digit Verification of cas no
The CAS Registry Mumber 77635-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,3 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77635-32:
(7*7)+(6*7)+(5*6)+(4*3)+(3*5)+(2*3)+(1*2)=156
156 % 10 = 6
So 77635-32-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H31NO2/c1-2-3-4-5-6-7-8-9-10-11-12-17-13-14-19(21)18(15-17)16-20-22/h13-16,20,22H,2-12H2,1H3/b18-16-
77635-32-6Relevant articles and documents
METHOD FOR PREPARATION OF 5-ALKYLSALICYLALDOXIMES AND APPLICATION THEREOF
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Paragraph 0019-0025, (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.