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Methyl linoleate - 95%, high purity , CAS No.112-63-0

    Grade & Purity:
  • ≥95%
In stock
Item Number
M102819
Grouped product items
SKU Size
Availability
Price Qty
M102819-1ml
1ml
≥10
$9.90
M102819-5ml
5ml
4
$23.90
M102819-25ml
25ml
1
$92.90
M102819-100ml
100ml
1
$331.90
M102819-500ml
500ml
2
$920.90

Basic Description

Synonyms (9Z,12Z)-9,12-Octadecadienoic acid methyl ester | EINECS 203-993-0 | L0078 | Methyl (Z,Z)-9,12-octadecadienoate | Q27137420 | Telfairic Acid methyl ester | (9Z,12Z)-Methyl octadeca-9,12-dienoate | (9Z,12Z)methyl octadeca-9,12-dienoate | FEMA NO. 3411, MET
Specifications & Purity ≥95%
Biochemical and Physiological Mechanisms Methyl linoleate may be used as a model compound in oxidation/peroxidation assays to evaluate the anti-peroxidation activity of fullerenes, ellagitannins and other natural products.
Storage Temp Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

It is more easily oxidized than conjugated methyl linoleate. Methyl linoleate may be used as a model compound in oxidation/peroxidation assays to evaluate the anti-peroxidation activity of fullerenes, ellagitannins and other natural products. For instance, the oxidation of methyl linoleate in organic solution and phosphatidylcholine (PC) in liposomal membranes induced by an azo initiator has often been used as a model for lipid peroxidation in vivo.
The oxidation of methyl linoleate in organic solution and phosphatidylcholine (PC) in liposomal membranes induced by an azo initiator has often been used as a model for lipid peroxidation in vivo.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Lipids and lipid-like molecules
Class Fatty Acyls
Subclass Lineolic acids and derivatives
Intermediate Tree Nodes Not available
Direct Parent Lineolic acids and derivatives
Alternative Parents Fatty acid methyl esters  Methyl esters  Monocarboxylic acids and derivatives  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular Framework Aliphatic acyclic compounds
Substituents Octadecanoid - Fatty acid methyl ester - Fatty acid ester - Methyl ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions.
External Descriptors fatty acid methyl ester

Names and Identifiers

Pubchem Sid 488195283
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488195283
IUPAC Name methyl (9Z,12Z)-octadeca-9,12-dienoate
INCHI InChI=1S/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-
InChIKey WTTJVINHCBCLGX-NQLNTKRDSA-N
Smiles CCCCCC=CCC=CCCCCCCCC(=O)OC
Isomeric SMILES CCCCC/C=C\C/C=C\CCCCCCCC(=O)OC
WGK Germany 1
Molecular Weight 294.47
Beilstein 1727610
Reaxy-Rn 1727613
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1727613&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

32 results found

Lot Number Certificate Type Date Item
H2104198 Certificate of Analysis May 12, 2025 M102819
D2501441 Certificate of Analysis Apr 03, 2025 M102819
D2102020 Certificate of Analysis Jan 09, 2025 M102819
K2321456 Certificate of Analysis Jun 09, 2023 M102819
K2321458 Certificate of Analysis Jun 09, 2023 M102819
K2321461 Certificate of Analysis Jun 02, 2023 M102819
K2321462 Certificate of Analysis Jun 02, 2023 M102819
H2318546 Certificate of Analysis May 30, 2023 M102819
H2318547 Certificate of Analysis May 30, 2023 M102819
H2318548 Certificate of Analysis May 30, 2023 M102819
D2313096 Certificate of Analysis Apr 03, 2023 M102819
D2313437 Certificate of Analysis Apr 03, 2023 M102819
D2313141 Certificate of Analysis Apr 03, 2023 M102819
D2313108 Certificate of Analysis Apr 03, 2023 M102819
D2312733 Certificate of Analysis Apr 03, 2023 M102819
D2312698 Certificate of Analysis Apr 03, 2023 M102819
D2312697 Certificate of Analysis Apr 03, 2023 M102819
D2313085 Certificate of Analysis Apr 03, 2023 M102819
C2315942 Certificate of Analysis Mar 09, 2023 M102819
C2315941 Certificate of Analysis Mar 09, 2023 M102819
C2315943 Certificate of Analysis Mar 09, 2023 M102819
C2308885 Certificate of Analysis Feb 28, 2023 M102819
C2308887 Certificate of Analysis Feb 28, 2023 M102819
C2308888 Certificate of Analysis Feb 28, 2023 M102819
C2308891 Certificate of Analysis Feb 28, 2023 M102819
C2308884 Certificate of Analysis Feb 28, 2023 M102819
B23241296 Certificate of Analysis Feb 20, 2023 M102819
K2208352 Certificate of Analysis Oct 27, 2022 M102819
F2215062 Certificate of Analysis Jun 11, 2022 M102819
F2215061 Certificate of Analysis Jun 11, 2022 M102819
F2215064 Certificate of Analysis Jun 11, 2022 M102819
F2215066 Certificate of Analysis Jun 11, 2022 M102819

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Chemical and Physical Properties

Solubility Solubility in water: insoluble Solubility in other solvents: miscible with DMF, fat solvents, oils
Sensitivity Light Sensitive,Air Sensitive
Refractive Index 1.462
Flash Point(°F) 235.4 °F
Flash Point(°C) 113 °C
Boil Point(°C) 192℃/4mmHg
Melt Point(°C) -35°C
Molecular Weight 294.500 g/mol
XLogP3 6.900
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 15
Exact Mass 294.256 Da
Monoisotopic Mass 294.256 Da
Topological Polar Surface Area 26.300 Ų
Heavy Atom Count 21
Formal Charge 0
Complexity 279.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 2
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 2
Covalently-Bonded Unit Count 1

Citations of This Product

1. Hongxu Lu, Yanxia Liu, Wenyue Shen, Yang Zhou, Xiangwei Ma, Shibo Sun, Xiaoying Dong, Fengyun Ji, Huiyan Tong, Jianqiang Xu, Gaohong He, Weiping Xu.  (2023)  Yeast enrichment facilitated lipid removal and bioconversion by black soldier fly larvae in the food waste treatment.  WASTE MANAGEMENT,  166  (152). 
2. Siyu Pan, Jun Yan, Xu Peng, Zhou Xu, Qi Zeng, Zhonghui Wang, Minzhong Zhao, Yi Chen.  (2023)  Y-Shaping All Components in Waste Cooking Oil-Derived Epoxidized Fatty Acid Methyl Esters toward a Leaching-Resistant Bioplasticizer.  ACS Sustainable Chemistry & Engineering,  11  (4): (1492–1501). 
3. Yuan Xue, Xueling Zhao, Hong Yuan, Hui Li.  (2022)  Oxidation reaction mechanism of hydrothermal carbon microspheres with applications to transesterification after sulfonation.  JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY,  98  (1): (66-76). 
4. Xiangying Yu, Xiaochun Chen, Yuting Li, Lin Li.  (2022)  Effect of Drying Methods on Volatile Compounds of Citrus reticulata Ponkan and Chachi Peels as Characterized by GC-MS and GC-IMS.  Foods,  11  (17): (2662). 
5. Jie Cheng, Hao Qin, Hongye Cheng, Zhen Song, Zhiwen Qi, Kai Sundmacher.  (2022)  Rational Screening of Deep Eutectic Solvents for the Direct Extraction of α-Tocopherol from Deodorized Distillates.  ACS Sustainable Chemistry & Engineering,  10  (25): (8216–8227). 
6. Yi-Tong Wang, Xiao-Man Wang, Di Gao, Fu-Ping Wang, Ya-Nan Zeng, Jun-Guo Li, Li-Qun Jiang, Qing Yu, Rui Ji, Le-Le Kang, Ya-Jun Wang, Zhen Fang.  (2022)  Efficient production of biodiesel at low temperature using highly active bifunctional Na-Fe-Ca nanocatalyst from blast furnace waste.  FUEL,  322  (124168). 
7. Xiao-Man Wang, Ya-Nan Zeng, Li-Qun Jiang, Yi-Tong Wang, Jun-Guo Li, Le-Le Kang, Rui Ji, Di Gao, Fu-Ping Wang, Qing Yu, Ya-Jun Wang, Ai-Min Ji, Zhen Fang.  (2022)  Highly stable NaFeO2-Fe3O4 composite catalyst from blast furnace dust for efficient production of biodiesel at low temperature.  INDUSTRIAL CROPS AND PRODUCTS,  182  (114937). 
8. Yi-Tong Wang, Di Gao, Jie Yang, Ya-Nan Zeng, Jun-Guo Li, Ya-Jun Wang, Xiao-Man Wang, Fu-Ping Wang, Qing Yu, Tian-Ji Liu, Shuang Cai, Zhen Fang.  (2022)  Highly stable heterogeneous catalysts from electric furnace dust for biodiesel production: Optimization, performance and reaction kinetics.  CATALYSIS TODAY,  404  (78). 
9. Yi-Tong Wang, Di Gao, Ya-Nan Zeng, Jun-Guo Li, Ai-Min Ji, Tian-Ji Liu, Shuang Cai, Wen-Jie Cong, Fu-Ping Wang, Qing Yu, Xiao-Man Wang, Zhen Fang.  (2022)  Efficient production of biodiesel with electric furnace dust impregnated in Na2CO3 solution.  Journal of Cleaner Production,  330  (129772). 
10. Qian Wang, Meiling Ge, Xuan Guo, Zhijun Li, Agen Huang, Fu Yang, Rong Guo.  (2021)  Hydrophobic poly(ionic liquid)s as “two-handed weapons”: Maximizing lipase catalytic efficiency in transesterification of soybean oil toward biodiesel.  APPLIED CATALYSIS A-GENERAL,  626  (118350). 
11. Wenchao Wang, Huili Liu, Fashe Li, Hua Wang, Xin Ma, Jingjing Li, Li Zhou, Quan Xiao.  (2021)  Effects of unsaturated fatty acid methyl esters on the oxidation stability of biodiesel determined by gas chromatography-mass spectrometry and information entropy methods.  RENEWABLE ENERGY,  175  (880). 
12. Hua-Ming Xiao, Shuai Zhao, Ru-Ting Fan, Dilshad Hussain, Xian Wang.  (2021)  Simultaneous determination of short-chain fatty alcohols in aged oil and biodiesels by stable isotope labeling assisted liquid chromatography-mass spectrometry.  TALANTA,  229  (122223). 
13. Dongren Cai, Guowu Zhan, Jingran Xiao, Shu-Feng Zhou, Ting Qiu.  (2021)  Design and synthesis of novel amphipathic ionic liquids for biodiesel production from soapberry oil.  RENEWABLE ENERGY,  168  (779). 
14. Xiao-Hui Yao, Yu-Shi Shen, Run-Ze Hu, Ming Xu, Jia-Xing Huang, Chen-Xi He, Fu-Liang Cao, Yu-Jie Fu, Dong-Yang Zhang, Wei-Guo Zhao, Li Liu, Tao Chen.  (2020)  The antioxidant activity and composition of the seed oil of mulberry cultivars.  Food Bioscience,  37  (100709). 
15. Gui-Lin Hu, Ya Gao, Xing-Rong Peng, Jun-Hong Liu, Hai-Guo Su, Yan-Jie Huang, Ming-Hua Qiu.  (2020)  Lactam ent-Kaurane Diterpene: A New Class of Diterpenoids Present in Roasted Beans of Coffea arabica.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,  68  (22): (6112–6121). 
16. Anlian Zhu, Wanlu Feng, Zhiyong Li, Shuang Cheng, Qianhan Chen, Dongshuang Fan, Yuanyang Guo, Lingjun Li, Jianji Wang.  (2020)  Cleaner enzymatic production of biodiesel with easy separation procedures triggered by a biocompatible hydrophilic ionic liquid.  GREEN CHEMISTRY,  22  (6): (1944-1951). 
17. Nisakorn Saengprachum, Dongren Cai, Mantian Li, Ling Li, Xiaocheng Lin, Ting Qiu.  (2019)  Acidic chitosan membrane as an efficient catalyst for biodiesel production from oleic acid.  RENEWABLE ENERGY,  143  (1488). 
18. Dongren Cai, Yiwei Xie, Ling Li, Jieyong Ren, Xiaocheng Lin, Ting Qiu.  (2018)  Design and synthesis of novel Brønsted-Lewis acidic ionic liquid and its application in biodiesel production from soapberry oil.  ENERGY CONVERSION AND MANAGEMENT,  166  (318). 
19. Huang Zhongping, Qiu Ruofeng, Huang Yilei, Liu Huijun, Pan Zaifa, Wang Lili.  (2018)  Rapid Analysis of Fatty Acid Composition in Polysorbate 80 by Gas Chromatography with On-line Pyrolytic Methylation Technique.  CHROMATOGRAPHIA,  81  (4): (669-675). 
20. Senan Ahmed M., Zhang Sicheng, Qin Shuhao, Chen Zhuqi, Yin Guochuan.  (2017)  Transformation of Methyl Linoleate to its Conjugated Derivatives with Simple Pd(OAc)2/Lewis Acid Catalyst.  JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY,  94  (12): (1481-1489). 
21. Weiwei Cheng, Guoqin Liu, Xinqi Liu.  (2017)  Effects of Fe3+ and Antioxidants on Glycidyl Ester Formation in Plant Oil at High Temperature and Their Influencing Mechanisms.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,  65  (20): (4167–4176). 
22. Jiebo Chen, Xinxiang Chen, Ying Zheng, Qinglu Li.  (2015)  Synergetic effect of ruthenium and basicity sites in the Ru–MgAl catalyst for hydrogen-free production of conjugated linoleic acids.  RSC Advances,  (26): (20248-20255). 
23. Xiao-Ying Qv, Qin-Fan Zhou, Jian-Guo Jiang.  (2014)  Ultrasound-enhanced and microwave-assisted extraction of lipid from Dunaliella tertiolecta and fatty acid profile analysis.  JOURNAL OF SEPARATION SCIENCE,  37  (20): (2991-2999). 
24. Ahmed M Senan,Sicheng Zhang,Miao Zeng,Zhuqi Chen,Guochuan Yin.  (2017-07-19)  Transformation of Unsaturated Fatty Acids/Esters to Corresponding Keto Fatty Acids/Esters by Aerobic Oxidation with Pd(II)/Lewis Acid Catalyst..  Journal of agricultural and food chemistry,  65  ((32)): (6912-6918). 
25. Zuhang Jin, Yiwei Zhao, Cheng Tao, Chao Zhang.  (2025)  An efficient Mo20/SiO2-La transesterification catalyst: The promoting role of La on anti-carbon deposition.  Journal of Environmental Chemical Engineering,  13  (115485). 
26. Xin-Yu Liu, Wen-Zhu Wang, Song-Po Yao, Xue-Ying Li, Rui-Min Han, Dangquan Zhang, Zhijun Zhao, Yapei Wang, Jian-Ping Zhang.  (2024)  Antioxidation Activity Enhancement by Intramolecular Hydrogen Bond and Non-Browning Mechanism of Active Ingredients in Rosemary: Carnosic Acid and Carnosol.  JOURNAL OF PHYSICAL CHEMISTRY B,  128  (31): (7627-7638). 
27. Jin Liu, Wei Pan, Suzhen Li, Yuanjun Nie, Xinyuan Bi, Xu Jing, Li Li.  (2025)  Green solvent-based high-throughput dispersive liquid-liquid microextraction for detecting strobilurin fungicides in environmental water samples.  JOURNAL OF CHROMATOGRAPHY A,  1749  (465888). 
28. Weiwei Cheng, Jiahe Xu, Xiaowen Wang, Xinyang Li, Yufeng Chen, Guoqin Liu, Xuxia Zhou, Yuting Ding, Shulai Liu.  (2024)  Multiple Mechanisms of Haematococcus pluvialis–Derived Carotenoids to Inhibit Glycidyl Ester Formation in Rice Oil and a Chemical Model at High Temperatures.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,  72  (34): (19177-19186). 
29. Shiwei Wang, Yuheng Wang, Rongjie Kong.  (2024)  New insights into the interaction between low-rank coal particles and clay minerals and its role in flotation responses.  Particuology,  94  (48). 
30. Jinxia Wang, Shuiqing He, Hong Yuan.  (2024)  Synthesizing a transesterification catalyst via a condensation reaction and assessment of the mechanism using density functional theory.  JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY,     

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