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Methyl Arachidate - analysis standard ,≥99.0% (GC), high purity , CAS No.1120-28-1
Basic Description
Synonyms
4B020CF8-8307-42EE-AE7F-95190AB03DFA | Eicosanoic acid methyl ester (FAME MIX) | Methyl icosanoate # | Methyl arachidate | Arachidic acid methyl ester | Q63398929 | UNII-0ZH75194U0 | Methyl icosanoate | EINECS 214-304-8 | A0900 | Eicosanoic acid-methyl es
Specifications & Purity
analytical standard, ≥99%(GC)
Storage Temp
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
analytical standard
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Fatty Acyls
Subclass
Fatty acid esters
Intermediate Tree Nodes
Not available
Direct Parent
Fatty acid methyl esters
Alternative Parents
Methyl esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic acyclic compounds
Substituents
Fatty acid methyl 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 fatty acid methyl esters. These are compounds containing a fatty acid that is esterified with a methyl group. They have the general structure RC(=O)OR', where R=fatty aliphatic tail or organyl group and R'=methyl group.
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Names and Identifiers
IUPAC Name
methyl icosanoate
INCHI
InChI=1S/C21H42O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21(22)23-2/h3-20H2,1-2H3
InChIKey
QGBRLVONZXHAKJ-UHFFFAOYSA-N
Smiles
CCCCCCCCCCCCCCCCCCCC(=O)OC
Isomeric SMILES
CCCCCCCCCCCCCCCCCCCC(=O)OC
WGK Germany
1
Molecular Weight
326.56
Beilstein
1791385
Reaxy-Rn
1791385
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1791385&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Refractive Index
1.4317
Flash Point(°C)
>113°C
Boil Point(°C)
215-216 °C/10 mmHg (lit.)
Melt Point(°C)
45-48°C
Molecular Weight
326.600 g/mol
XLogP3
10.100
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
19
Exact Mass
326.318 Da
Monoisotopic Mass
326.318 Da
Topological Polar Surface Area
26.300 Ų
Heavy Atom Count
23
Formal Charge
0
Complexity
238.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
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).
2.
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).
3.
Hongxu Zhou, Qing Jiang, Xin He, Xian Fu, Jun-Yan Liu.
(2024)
A complementary method with PFBBr-derivatization based on GC-EI-MS platform for the simultaneous quantitation of short-, medium- and long -chain fatty acids in murine plasma and feces samples. Analytical Methods,
4.
Dengke Li, Qinghao Shi, Fengbing Liang, Dexin Feng.
(2024)
The Green Synthesis of Biodiesel via Esterification in Water Catalyzed by the Phosphotungstic Acid–Functionalized Hydrophobic MCM–41 Catalyst. Catalysts,
14
(2):
(142).
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4 Citations
E2431308