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112-63-0

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112-63-0 Usage

General Description

Methyl cis,cis-9,12-octadecadienoate, also known as methyl linoleate, is a chemical compound that belongs to the class of organic compounds known as fatty acid esters. It is a methyl ester derivative of linoleic acid, which is an essential polyunsaturated omega-6 fatty acid found in many vegetable oils. Methyl cis,cis-9,12-octadecadienoate is commonly used in the synthesis of various organic compounds and is also found naturally in plant oils, such as safflower oil and sunflower oil. It is used in the production of cosmetics, surfactants, and lubricants due to its moisturizing and emollient properties. Additionally, it is often used as a flavoring agent in food products and as a fragrance ingredient in perfumes and personal care products.

Check Digit Verification of cas no

The CAS Registry Mumber 112-63-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 112-63:
(5*1)+(4*1)+(3*2)+(2*6)+(1*3)=30
30 % 10 = 0
So 112-63-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h7-8,10-11H,3-6,9,12-18H2,1-2H3/b8-7-,11-10-

112-63-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L07450)  Methyl linoleate, 95%   

  • 112-63-0

  • 1g

  • 306.0CNY

  • Detail
  • Alfa Aesar

  • (L07450)  Methyl linoleate, 95%   

  • 112-63-0

  • 5g

  • 598.0CNY

  • Detail
  • Sigma

  • (L1876)  Methyllinoleate  ≥99% (GC)

  • 112-63-0

  • L1876-1G

  • 465.66CNY

  • Detail
  • Sigma

  • (L1876)  Methyllinoleate  ≥99% (GC)

  • 112-63-0

  • L1876-5G

  • 918.45CNY

  • Detail
  • Sigma

  • (L1876)  Methyllinoleate  ≥99% (GC)

  • 112-63-0

  • L1876-10G

  • 1,678.95CNY

  • Detail
  • Sigma

  • (L1876)  Methyllinoleate  ≥99% (GC)

  • 112-63-0

  • L1876-25G

  • 2,293.20CNY

  • Detail
  • Sigma-Aldrich

  • (62280)  Methyllinoleate  analytical standard

  • 112-63-0

  • 62280-5ML

  • 764.01CNY

  • Detail
  • USP

  • (1430327)  Methyllinoleate  United States Pharmacopeia (USP) Reference Standard

  • 112-63-0

  • 1430327-5X50MG

  • 4,662.45CNY

  • Detail
  • Supelco

  • (46950-U)  cis-9,cis-12-Octadecadienoicacidmethylester  certified reference material, 10 mg/mL in heptane

  • 112-63-0

  • 46950-U

  • 415.35CNY

  • Detail

112-63-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl linoleate

1.2 Other means of identification

Product number -
Other names 9,12-Octadecadienoic acid (Z,Z)-, methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Fuels and fuel additives,Lubricants and lubricant additives
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:112-63-0 SDS

112-63-0Relevant articles and documents

Two new glyceroglycolipids from the fruits of Cucurbita moschata

Jianga, Zhi-Guo,Dua, Qi-Zhen

, p. 157 - 159 (2009)

Aphytochemical study of Cucurbita moschata resulted in the characterisation of two new glyceroglycolipids, 1-O-(9Z, 12Z,15Z-octadecatrienoyl)-3-0-[β- D-galactopyranosyl-(1-6)-0-p-D-galactopyranosyl-(1?6)-O-p-D-galactopyranosyl] glycerol (1) and 1-0-(9Z,12

A Facile Method for Activation of Carboxylic Acids

Murata, Shizuaki

, p. 3597 - 3598 (1984)

-

Brown,Stoner

, p. 4,6 (1937)

Linoleic acid, α-linolenic acid, and monolinolenins as antibacterial substances in the heat-processed soybean fermented with Rhizopus oligosporus

Kusumah, Dewi,Maeda, Isamu,Murakami, Mai,Wakui, Misaki,Xie, Xiaonan,Yukihito, Kabuyama

, p. 1285 - 1290 (2020)

Antibacterial activities against Staphylococcus aureus and Bacillus subtilis were found in an ethanol fraction of tempe, an Indonesian fermented soybean produced using Rhizopus oligosporus. The ethanol fraction contained free fatty acids, monoglycerides, and fatty acid ethyl esters. Among these substances, linoleic acid and α-linolenic acid exhibited antibacterial activities against S. aureus and B. subtilis, whereas 1-monolinolenin and 2-monolinolenin exhibited antibacterial activity against B. subtilis. The other free fatty acids, 1-monoolein, monolinoleins, ethyl linoleate, and ethyl linolenate did not exhibit bactericidal activities. These results revealed that R. oligosporus produced the long-chain polyunsaturated fatty acids and monolinolenins as antibacterial substances against the Gram-positive bacteria during the fungal growth and fermentation of heat-processed soybean.

Bioactive tigliane diterpenoids from the latex of Euphorbia fischeriana

Deng, Yan-Yan,Qu, Bo,Zhan, Zhong-Lang,Wang, An-Qi,Zhou, Wei,Jia, Ming-Yue,Hua, Juan,Luo, Shi-Hong

, p. 179 - 187 (2021)

Latex is a type of sticky endogenous fluids derived from diverse plants including Euphorbia fischeriana, and is of great scientific and commercial values. In the current study, it was demonstrated that the latex extracted from E. fischeriana strongly respelled the growth of cotton bollworm, Helicoverpa armigera. Using spectroscopic methods, HPLC, and GC-MS analyses, six aliphatic tigliane diterpenoids were isolated from the latex of E. fischeriana, among which three compounds (2, 3, and 5) were new. Two major compounds (1 and 4) exhibited remarkable antifeedant activity against H. armigera, with EC50 values at 2.59 and 15.32 μg/cm2, respectively. In addition, the quantification analysis of diterpenoids in different organs indicated that 4 was the most abundant constituent and was highly accumulated in the latex. Collectively, the current study highlighted that the diterpenoids in latex of E. fischeriana had a considerable antifeedant function against H. armigera, which might be employed for the future development of natural insecticides for organic farming.

Branched alkyl sulfonate anionic surfactant and preparation process thereof

-

Paragraph 0090-0091, (2021/02/10)

The invention discloses a branched alkyl sulfonate anionic surfactant and a preparation process thereof, and belongs to the field of fine chemical surfactants. The method comprises the steps of (1) conducting a esterification carboxyl-terminated reaction, specifically, catalyzing oleic acid or linoleic acid and fatty alcohol to be subjected to esterification reaction by adopting organic acid as acatalyst to prepare an alkyl oleate or alkyl linoleate compound; and (2) conducting a double bond addition sulfonation reaction, specifically, in the presence of the catalyst, carrying out sulfonationreaction with the alkyl oleate compound or the alkyl linoleate compound obtained in the step (1) by taking low-carbon alcohol and deionized water as solvents and sodium hydrogen sulfite as a sulfonation reagent to prepare the branched alkyl sulfonate anionic surfactant. The synthesized branched alkyl sulfonate anionic surfactant product can effectively reduce the surface tension of an aqueous solution, and is good in solubility, large in initial foaming amount, high in defoaming speed and excellent in surfactant performance. The method has the advantages of simple process operation, few sidereactions, energy saving and environmental protection.

Highly ordered mesoporous functionalized pyridinium protic ionic liquids framework as efficient system in esterification reactions for biofuels production

Luque, Rafael,Rajabi, Fatemeh

, (2020/11/09)

Polysiloxane acidic ionic liquids containing pyridinium trifluoroacetate salts (PMO-Py-IL) were synthesized from pyridine containing organosilane precursors. Characterization by SEM, XRD, TGA, and nitrogen porosimetry confirmed that both pyridinium cation and trifluoroacetate anion were successfully incorporated within the organosilica network. The resulting organic-inorganic hybrid nanomaterial (PMO-Py-IL) was studied as nanocatalyst in free fatty acids esterification into biodiesel-like compounds. Remarkably, the synergistic hydrophilic/hydrophobic effect of pyridinium and trifluoroacetate ionic liquid in the well-ordered channels of PMO-Py-IL nanomaterial enhanced the activity toward sustainable biodiesel-like esters production. More importantly, PMO-Py-IL nanocatalyst also exhibited an exceptional activity and stability. The catalyst could be easily separated to reuse at least in ten reactions runs preserving almost intact its catalytic activity under otherwise identical conditions to those employed for the fresh catalysts.

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