42235-38-1

  • Product Name:dimethyl icosanedioate
  • Molecular Formula:
  • Purity:99%
  • Molecular Weight:370.573
Inquiry

Product Details

Quality Manufacturer Supply High Purity dimethyl icosanedioate 42235-38-1 On Stock

  • Molecular Formula:C22H42O4
  • Molecular Weight:370.573
  • Melting Point:66 °C 
  • Boiling Point:223 °C / 2mmHg 

Dimethyl icosanedioate(Cas 42235-38-1) Usage

Description

White to Almost white powder to crystal.

Uses

Dimethyl icosanedioate is commonly used as an additive in lubricating oils and lubricants to improve the lubrication performance and durability of products. It can also serve as a raw material for softeners in the textile, plastic, and rubber industries. Additionally, it can be used as an intermediate in chemical synthesis for synthesizing resins, dyes, pharmaceuticals, and other chemicals.

InChI:InChI=1S/C22H42O4/c1-25-21(23)19-17-15-13-11-9-7-5-3-4-6-8-10-12-14-16-18-20-22(24)26-2/h3-20H2,1-2H3

42235-38-1 Relevant articles

A Facile and Efficient Method for the Synthesis of Labeled and Unlabeled Very Long Chain Polyunsaturated Fatty Acids

Hamberg, Mats

, p. 489 - 494 (2021/04/19)

Several methods are available for elonga...

Cysteine-Targeted Insecticides against A. gambiae Acetylcholinesterase Are Neither Selective nor Reversible Inhibitors

Gorecki, Lukas,Andrys, Rudolf,Schmidt, Monika,Kucera, Tomas,Psotka, Miroslav,Svobodova, Barbora,Hrabcova, Veronika,Hepnarova, Vendula,Bzonek, Petr,Jun, Daniel,Kuca, Kamil,Korabecny, Jan,Musilek, Kamil

, p. 65 - 71 (2019/12/25)

Acetylcholinesterase cysteine-targeted i...

Metathesis of renewable polyene feedstocks – Indirect evidences of the formation of catalytically active ruthenium allylidene species

Kovács, Ervin,Sághy, Péter,Turczel, Gábor,Tóth, Imre,Lendvay, Gy?rgy,Domján, Attila,Anastas, Paul T.,Tuba, Róbert

supporting information, p. 213 - 217 (2017/09/12)

Cross-metathesis (CM) of conjugated poly...

Synthesis of [3]rotaxanes that utilize the catalytic activity of a macrocyclic phenanthroline-Cu complex: Remarkable effect of the length of the axle precursor

Yamashita, Yoshiaki,Mutoh, Yuichiro,Yamasaki, Ryu,Kasama, Takeshi,Saito, Shinichi

supporting information, p. 2139 - 2145 (2015/02/19)

[3]Rotaxanes, which consist of one macro...

42235-38-1 Process route

methyl α-eleostearate
4175-47-7

methyl α-eleostearate

nonane
111-84-2

nonane

decane
124-18-5

decane

n-Undecane
1120-21-4

n-Undecane

dodecane
112-40-3

dodecane

Tridecane
629-50-5

Tridecane

tetradecane
629-59-4

tetradecane

Hexadecane
544-76-3

Hexadecane

methyl tridecanoate
1731-88-0

methyl tridecanoate

methyl myristoate
124-10-7

methyl myristoate

pentadecanoic acid methyl ester
7132-64-1

pentadecanoic acid methyl ester

hexadecanoic acid methyl ester
112-39-0

hexadecanoic acid methyl ester

methyl margarate
1731-92-6

methyl margarate

Methyl stearate
112-61-8

Methyl stearate

dimethyl heptadecane-1,17-dioate
19102-92-2

dimethyl heptadecane-1,17-dioate

dimethyl 1,18-octadecanedioate
1472-93-1

dimethyl 1,18-octadecanedioate

dimethyl 1,19-nonadecandioate
23130-41-8

dimethyl 1,19-nonadecandioate

1,18-octadecanoic acid dimethyl ester
42235-38-1

1,18-octadecanoic acid dimethyl ester

Methyl-2,6,10,14-tetramethylhexadecanoat

Methyl-2,6,10,14-tetramethylhexadecanoat

Conditions
Conditions Yield
methyl α-eleostearate; With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; In toluene; at 100 ℃; for 2h; Schlenk technique; Inert atmosphere;
With palladium on activated charcoal; hydrogen; In ethanol; toluene; at 20 ℃; Schlenk technique;
 
10-bromodecanoic acid methyl ester
26825-94-5

10-bromodecanoic acid methyl ester

(3Z)-8-bromooct-3-ene
76971-26-1

(3Z)-8-bromooct-3-ene

1,18-octadecanoic acid dimethyl ester
42235-38-1

1,18-octadecanoic acid dimethyl ester

methyl 15(Z)-octadecenoate
10411-39-9

methyl 15(Z)-octadecenoate

3,13-hexadecadiene

3,13-hexadecadiene

Conditions
Conditions Yield
With manganese; (1,2-dimethoxyethane)dichloronickel(II); 4,4',4-tri-tert-butyl-2,2':6',2-terpyridine; In N,N-dimethyl-formamide; at 40 ℃; for 4h;
0.22 mmol

42235-38-1 Upstream products

  • 67-56-1
    67-56-1

    methanol

  • 2424-92-2
    2424-92-2

    octadecane-1,18-dicarboxylic acid

  • 53481-02-0
    53481-02-0

    dimethyl 10-eicosenedioate

  • 4175-47-7
    4175-47-7

    methyl α-eleostearate

42235-38-1 Downstream products

  • 1767-98-2
    1767-98-2

    20-methoxy-20-oxoicosanoic acid

  • 14296-16-3
    14296-16-3

    1,20-dibromoeicosane

  • 838888-27-0
    838888-27-0

    7-benzyl-16-(20-bromo-eicosyl)-1,4,10,13-tetraoxa-7,16-diaza-cyclooctadecane

  • 6250-70-0
    6250-70-0

    1,19-nonadecanedioic acid