- Product Name 11-hydroxy-10-icosanone
- cas 4443-65-6
- purity 99%
Reputable factory supply 11-hydroxy-10-icosanone 4443-65-6 in bulk at low price
- Molecular Formula: C20H40 O2
- Molecular Weight: 312.536
- Vapor Pressure: 1.05E-05mmHg at 25°C
- Boiling Point: 332.4°Cat760mmHg
- Flash Point: 141.3°C
- PSA: 37.30000
- Density: 0.883g/cm3
- LogP: 6.19780
11-hydroxy-10-icosanone(Cas 4443-65-6) Usage
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Chemical structure |
A 20-carbon chain with a hydroxy group attached to the 11th carbon and a carbonyl group at the 10th carbon. |
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Classification |
A ketone, due to the presence of the carbonyl group. |
|
Natural occurrence |
Found in the natural waxes of plants and animals. |
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Industrial applications |
Used as a fragrance ingredient, flavoring agent, and in the production of cosmetics and pharmaceuticals. |
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Biological activities |
Exhibits potential antimicrobial and antioxidant properties. |
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Research and development |
Valued for further research due to its potential applications and biological activities. |
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Molecular weight |
Approximately 312 g/mol (calculated from the molecular formula). |
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Physical state |
Likely a liquid or a solid at room temperature, depending on the specific conditions. |
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Solubility |
Soluble in organic solvents, such as ethanol or acetone, due to its nonpolar nature. |
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Reactivity |
May react with other compounds containing carbonyl groups or hydroxy groups, such as in condensation or substitution reactions. |
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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. |
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General Description |
11-hydroxy-10-icosanone is a chemical compound known for its fatty acid derived structure, with a 20-carbon chain and a hydroxy group attached to the 11th carbon. It is classified as a ketone, with a carbonyl group located at the 10th carbon atom. This chemical is commonly found in the natural waxes of plants and animals, and it is known for its potential applications in various industries, including as a fragrance ingredient, a flavoring agent, and in the production of cosmetics and pharmaceuticals. Additionally, 11-hydroxy-10-icosanone has been studied for its potential biological activities, including its antimicrobial and antioxidant properties, which make it a valuable compound for further research and development. |
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
4443-65-6 Relevant articles
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 develo...
Catalytic action of azolium salts. VI. Preparation of benzoins and acyloins by condensation of aldehydes catalyzed by azolium salts
Miyashita,Suzuki,Iwamoto,Higashino
, p. 2633 - 2635 (2007/10/02)
Benzoins 4 (2-hydroxyethanones substitut...
Acyloin condensation by thiazolium ion catalysis: Butyroin
Stetter,Kuhlmann
, p. 170 - 170 (2017/06/02)
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4443-65-6 Process route
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112-31-2
caprinaldehyde
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4443-65-6
11-hydroxy-eicosan-10-one
| Conditions | Yield |
|---|---|
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With
3-benzyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazol-3-ium chloride; triethylamine;
In
ethanol;
at 80 ℃;
for 1.5h;
Inert atmosphere;
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85%
|
|
With
1,3-dimethylbenzimidazolium Iodide; 1,8-diazabicyclo[5.4.0]undec-7-ene;
In
1,4-dioxane;
for 3h;
Heating;
|
84%
|
-
-
110-42-9
Methyl decanoate
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-
4443-65-6
11-hydroxy-eicosan-10-one
| Conditions | Yield |
|---|---|
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With
sodium; xylene;
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4443-65-6 Upstream products
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110-42-9
Methyl decanoate
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110-38-3
decanoic acid ethyl ester
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112-31-2
caprinaldehyde