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4443-65-6

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4443-65-6 Usage

Chemical structure

A 20-carbon chain with a hydroxy group attached to the 11th carbon and a carbonyl group at the 10th carbon.

Classification

A ketone, due to the presence of the carbonyl group.

Natural occurrence

Found in the natural waxes of plants and animals.

Industrial applications

Used as a fragrance ingredient, flavoring agent, and in the production of cosmetics and pharmaceuticals.

Biological activities

Exhibits potential antimicrobial and antioxidant properties.

Research and development

Valued for further research due to its potential applications and biological activities.

Molecular weight

Approximately 312 g/mol (calculated from the molecular formula).

Physical state

Likely a liquid or a solid at room temperature, depending on the specific conditions.

Solubility

Soluble in organic solvents, such as ethanol or acetone, due to its nonpolar nature.

Reactivity

May react with other compounds containing carbonyl groups or hydroxy groups, such as in condensation or substitution reactions.

Safety

As with any chemical compound, appropriate safety measures should be taken when handling 11-hydroxy-10-icosanone, including the use of gloves, eye protection, and proper ventilation.

Check Digit Verification of cas no

The CAS Registry Mumber 4443-65-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4443-65:
(6*4)+(5*4)+(4*4)+(3*3)+(2*6)+(1*5)=86
86 % 10 = 6
So 4443-65-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H40O2/c1-3-5-7-9-11-13-15-17-19(21)20(22)18-16-14-12-10-8-6-4-2/h19,21H,3-18H2,1-2H3

4443-65-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-hydroxyicosan-10-one

1.2 Other means of identification

Product number -
Other names 11-Hydroxy-10-icosanone

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:4443-65-6 SDS

4443-65-6Downstream Products

4443-65-6Relevant articles and documents

Separation and complexation of palladium(II) with a new soft N-donor ligand 6,6′-bis(5,6-dinonyl-1,2,4-triazin-3-yl)-2,2′-bipyridine (C9-BTBP) in nitric acid medium

Zhang, Anyun,Xu, Lei,Lei, Gaoming

, p. 6374 - 6383 (2016/07/16)

Soft N-donor bis-triazine ligands developed for the separation of minor actinides (MAs) from lanthanides have been intensively studied for the past two decades. However, the investigation on the recovery and complexation of fission products Pd(ii) with these ligands has rarely been reported to date. Herein, the synthesis, and solvent extraction of Pd(ii) and some typical metals from HNO3 solutions as well as Pd(ii) complexation with a new soft N-donor ligand C9-BTBP were presented. The C9-BTBP ligand exhibited high extraction capability and high selectivity for Pd(ii) in HNO3 solution. Both 1:1 and 2:1 Pd(ii)-C9-BTBP complexes were found in solution by a combination of ESI-MS and 1H NMR titration experiments. A solid binuclear Pd(ii) complex [Pd2(NO3)4·(C9-BTBP)]·2.5H2O was synthesized and characterized by elemental analysis, DSC-TGA and 1H NMR. This is the first example that a binuclear Pd(ii) complex with any N-donor bis-triazine ligand has been confirmed both in solution and in the solid state.

Acyloin condensation by thiazolium ion catalysis: Butyroin

Stetter,Kuhlmann

, p. 170 - 170 (2017/06/02)

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