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DIMETHYL TETRADECANEDIOATE

  • CAS No.: 5024-21-5
  • Purity: 99%
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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

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

methanol
67-56-1

methanol

1,14-tetradecanedioic acid
821-38-5

1,14-tetradecanedioic acid

dimethyl tetradecanedioate
5024-21-5

dimethyl tetradecanedioate

Conditions
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 ℃;
suberic acid monomethyl ester
3946-32-5

suberic acid monomethyl ester

dimethyl tetradecanedioate
5024-21-5

dimethyl tetradecanedioate

Conditions
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

  • 67-56-1
    67-56-1

    methanol

  • 112-80-1
    112-80-1

    cis-Octadecenoic acid

  • 3946-32-5
    3946-32-5

    suberic acid monomethyl ester

  • 821-38-5
    821-38-5

    1,14-tetradecanedioic acid

5024-21-5 Downstream products

  • 821-38-5
    821-38-5

    1,14-tetradecanedioic acid

  • 50515-99-6
    50515-99-6

    methyl hydrogen tetradecanedioate

  • 19812-64-7
    19812-64-7

    1,14-tetradecanediol

  • 50515-98-5
    50515-98-5

    14-hydroxytetradecanoic acid methyl ester

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