High Quality Chinese Manufacturer supply 5024-21-5 DIMETHYL TETRADECANEDIOATE
- Molecular Formula: C16H30 O4
- Molecular Weight: 286.412
- Vapor Pressure: 0.000213mmHg at 25°C
- Melting Point: 43 °C
- Boiling Point: 326.6 °C at 760 mmHg
- Flash Point: 146.4 °C
- PSA: 52.60000
- Density: 0.955 g/cm3
- LogP: 4.01360
DIMETHYL TETRADECANEDIOATE(Cas 5024-21-5) Usage
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General Description |
DIMETHYL TETRADECANEDIOATE is a chemical compound that belongs to the class of organic compounds known as dicarboxylic acids and their derivatives. It is a colorless liquid with a fruity odor and is commonly used as a fragrance ingredient in various cosmetic and personal care products. It is also used as a flavor enhancer in food products. Additionally, it is utilized as an intermediate in the production of other chemicals and as a plasticizer in the manufacture of plastics and resins. DIMETHYL TETRADECANEDIOATE is considered to have low toxicity and is generally regarded as safe for use in consumer products when used in accordance with regulations and guidelines. |
InChI:InChI=1/C16H30O4/c1-19-15(17)13-11-9-7-5-3-4-6-8-10-12-14-16(18)20-2/h3-14H2,1-2H3
5024-21-5 Relevant articles
Efficient Palladium-Catalyzed Carbonylation of 1,3-Dienes: Selective Synthesis of Adipates and Other Aliphatic Diesters
Yang, Ji,Liu, Jiawang,Ge, Yao,Huang, Weiheng,Ferretti, Francesco,Neumann, Helfried,Jiao, Haijun,Franke, Robert,Jackstell, Ralf,Beller, Matthias
supporting information, p. 9527 - 9533 (2021/03/08)
The dicarbonylation of 1,3-butadiene to ...
Discovery and Pharmacological Studies of 4-Hydroxyphenyl-Derived Phosphonium Salts Active in a Mouse Model of Visceral Leishmaniasis
Manzano, José Ignacio,Cueto-Díaz, Eduardo J.,Olías-Molero, Ana Isabel,Perea, Ana,Herraiz, Tomás,Torrado, Juan J.,Alunda, José María,Gamarro, Francisco,Dardonville, Christophe
, p. 10664 - 10675 (2019/12/04)
We report the discovery of new 4-hydroxy...
Improved Syntheses of Benzyl Hydraphile Synthetic Cation-Conducting Channels
Curvey, Nichole S.,Luderer, Sarah E.,Walker, John K.,Gokel, George W.
, p. 2771 - 2779 (2015/02/19)
The tris(macrocycle)s that function in b...
Metal/bromide autoxidation of triglycerides for the preparation of FAMES to improve the cold-flow characteristics of biodiesel
Phung, Peter,Rowlands, William N.,Thiyakesan, Appadurai,Benndorf, Paul,Masters, Anthony F.,Maschmeyer, Thomas
, p. 162 - 168 (2014/07/07)
Triglyceride autoxidation using a homoge...
5024-21-5 Process route
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67-56-1
methanol
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821-38-5
1,14-tetradecanedioic acid
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-
5024-21-5
dimethyl tetradecanedioate
| Conditions | Yield |
|---|---|
|
With
thionyl chloride;
for 24h;
Inert atmosphere;
|
100%
|
|
With
sulfuric acid;
Heating;
|
|
|
With
thionyl chloride;
at 20 ℃;
for 6h;
|
|
|
With
thionyl chloride;
at 20 ℃;
|
-
-
3946-32-5
suberic acid monomethyl ester
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-
5024-21-5
dimethyl tetradecanedioate
| Conditions | Yield |
|---|---|
|
In
methanol;
(electrolysis);
|
|
|
With
potassium hydroxide;
In
methanol;
at 25 ℃;
electrolysis, Pt-electrodes, 150 mA/cm-2;
|
|
|
With
potassium hydroxide;
In
methanol; di-isopropyl ether; cyclohexane; acetonitrile;
Electrolysis;
|
72 %Spectr.
|
5024-21-5 Upstream products
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67-56-1
methanol
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112-80-1
cis-Octadecenoic acid
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3946-32-5
suberic acid monomethyl ester
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821-38-5
1,14-tetradecanedioic acid
5024-21-5 Downstream products
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821-38-5
1,14-tetradecanedioic acid
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50515-99-6
methyl hydrogen tetradecanedioate
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19812-64-7
1,14-tetradecanediol
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50515-98-5
14-hydroxytetradecanoic acid methyl ester