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9,10-DIHYDROXYSTEARIC ACID

  • CAS:120-87-6
  • purity:99%
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Factory Sells Best Quality 9,10-DIHYDROXYSTEARIC ACID 120-87-6 with GMP standards

  • Molecular Formula: C18H36O4
  • Molecular Weight: 316.481
  • Appearance/Colour: Waxy, off-white solid 
  • Vapor Pressure: 2.68E-11mmHg at 25°C 
  • Melting Point: 90°C 
  • Refractive Index: 1.4434 (estimate) 
  • Boiling Point: 481.618 °C at 760 mmHg 
  • PKA: 4.78±0.10(Predicted) 
  • Flash Point: 259.18 °C 
  • PSA: 77.76000 
  • Density: 1.001 g/cm3 
  • LogP: 4.27410 

9,10-DIHYDROXYSTEARIC ACID(Cas 120-87-6) Usage

Definition

ChEBI: A hydroxy-fatty acid formally derived from stearic acid by hydroxy substitution at positions 9 and 10.

InChI:InChI=1/C18H36O4.Li/c1-2-3-4-5-7-10-13-16(19)17(20)14-11-8-6-9-12-15-18(21)22;/h16-17,19-20H,2-15H2,1H3,(H,21,22);/q;+1/p-1

120-87-6 Relevant articles

ON THE STRUCTURE OF MICELLES.

Menger,Doll

, p. 1109 - 1113 (1984)

Kinetic studies of micellar olefin oxida...

The action of hypochlorous acid on phosphatidylcholine liposomes in dependence on the content of double bonds. Stoichimetry and NMR analysis

Arnhold, J.,Panasenko, O. M.,Schiller, J.,Vladimirov, Yu. A.,Arnold, K.

, p. 55 - 64 (1995)

Kinetics of the consumption of hypochlor...

THE ELCTRICAL CONDUCTANCE OF MOLTEN LEAD(II) 9,10-DIHYDROXYOCTADECANOATE AND SOME BINARY MIXTURES WITH LEAD(II) OCTADECANOATE

Akanni, M. Sola,Mbaneme, P. Chuckwulozie

, p. 3357 - 3366 (1986)

Data are presented for electrical conduc...

STEREOCHEMISTRY OF β-HYDROXYDODECANOYL THIOESTER DEHYDRATION CATALYZED BY FATTY ACID SYNTHETASE FROM BREVIBACTERIUM AMMONIAGENES

Saito, Kazuki,Kawaguchi, Akihiko,Seyama, Yousuke,Yamakawa, Tamio,Okuda, Shigenobu

, p. 1689 - 1692 (1982)

The pro-4S hydrogen of trans-α,β-dodecen...

PROCESS FOR THE PREPARATION OF HYDROPEROXY ALCOHOLS USING A HETEROGENOUS CATALYST

-

Page/Page column 14-16-20, (2021/07/02)

The present invention relates to a proce...

Design, synthesis and gelation of low molecular weight organo-gelators derived from oleic acid via, amidation

Gupta, Gaurav R.,Joshi, Narendra S.,Phalak, Raju P.,Waghulde, Govinda P.

, p. 1109 - 1116 (2021/11/17)

In recent decades, gels have been widely...

Oxidative carbon-carbon bond cleavage of 1,2-diols to carboxylic acids/ketones by an inorganic-ligand supported iron catalyst

Chen, Weiming,Xie, Xin,Zhang, Jian,Qu, Jian,Luo, Can,Lai, Yaozhu,Jiang, Feng,Yu, Han,Wei, Yongge

supporting information, p. 9140 - 9146 (2021/11/23)

The carbon-carbon bond cleavage of 1,2-d...

FUNCTIONAL LIPID DERIVATIVES AND USES THEREOF

-

Page/Page column 5, (2021/11/26)

The present disclosure relates to compou...

120-87-6 Process route

cis-Octadecenoic acid
112-80-1,2027-47-6

cis-Octadecenoic acid

Dihydroxystearic Acid
120-87-6

Dihydroxystearic Acid

9,10-epoxystearic acid
2443-39-2,13980-07-9,16833-55-9,17682-84-7,17682-85-8,24560-98-3,38003-74-6,38003-76-8

9,10-epoxystearic acid

Conditions
Conditions Yield
With zinc(II) tungstate; dihydrogen peroxide; acetic acid; at 30 ℃; for 5h; Temperature; Reagent/catalyst; Catalytic behavior;
20%
17%
With zinc(II) tungstate; dihydrogen peroxide; acetic acid; at 30 ℃; for 5h; Temperature; Reagent/catalyst; Catalytic behavior;
12%
8%
cis-Octadecenoic acid
112-80-1,2027-47-6

cis-Octadecenoic acid

azelaic acid
123-99-9,26776-28-3

azelaic acid

threo-9,10-dihydroxyoctadecanoic acid
120-87-6,2391-05-1,3639-32-5,10067-09-1,20831-62-3,20831-68-9,38003-70-2

threo-9,10-dihydroxyoctadecanoic acid

erythro-9,10-dihydroxystearic acid
120-87-6,2391-05-1,3639-32-5,10067-09-1,20831-62-3,20831-68-9,38003-70-2

erythro-9,10-dihydroxystearic acid

10-hydroxystearic acid
638-26-6

10-hydroxystearic acid

Conditions
Conditions Yield
at 120 ℃; durch geblasenes Waloel katalysierten Autoxydation;

120-87-6 Upstream products

  • 112-80-1
    112-80-1

    cis-Octadecenoic acid

  • 112-79-8
    112-79-8

    Elaidic acid

  • 5829-48-1
    5829-48-1

    9,10-dichlorooctadecanoic acid

  • 6085-36-5
    6085-36-5

    oleic anhydride

120-87-6 Downstream products

  • 123-99-9
    123-99-9

    azelaic acid

  • 505-48-6
    505-48-6

    octane-1,8-dioic acid

  • 124-19-6
    124-19-6

    nonan-1-al

  • 2553-17-5
    2553-17-5

    azelaic acid semialdehyde

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