Methyl ricinoleate - analytical standard, ≥99%(GC) , CAS No.141-24-2

CAS: 141-24-2 Cat. No.: M101313 Molecular Weight: 312.49 Beilstein Registry Number: 6132055 EC Number: 205-472-3

GRADE & PURITY Analytical standard, ≥99%(GC)

Synonyms

Q27271321 | AS-70362 | Methyl ricinoleate, European Pharmacopoeia (EP) Reference Standard | Sulfisoxazole dialamine | AI3-10523 | DTXCID509169 | NCGC00248854-01 | 3H-Imidazo[4,5-b]pyridine,2-[2-methoxy-4-(methylsulfinyl)phenyl]- | Ricinolic Acid Methyl Es

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Overview

Application：

Methyl ricinoleate is an enantiomerically renewable compound commercially obtained by the transesterification from castor oil, commonly used in cosmetics, plasticizers, lubricating oils and fine-chemical industries.

Specifications

Synonyms

Q27271321 | AS-70362 | Methyl ricinoleate, European Pharmacopoeia (EP) Reference Standard | Sulfisoxazole dialamine | AI3-10523 | DTXCID509169 | NCGC00248854-01 | 3H-Imidazo[4, 5-b]pyridine, 2-[2-methoxy-4-(methylsulfinyl)phenyl]- | Ricinolic Acid Methyl Es

Specifications & Purity

analytical standard, ≥99%(GC)

Storage

Store at -20°C, Argon charged

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Grade

Analytical standard

Purity

≥99%(GC)

Names and Identifiers

• Canonical Smiles: CCCCCCC(CC=CCCCCCCCC(=O)OC)O
• IUPAC Name: methyl (Z,12R)-12-hydroxyoctadec-9-enoate
• InChIKey: XKGDWZQXVZSXAO-ADYSOMBNSA-N
• INCHI: 1S/C19H36O3/c1-3-4-5-12-15-18(20)16-13-10-8-6-7-9-11-14-17-19(21)22-2/h10,13,18,20H,3-9,11-12,14-17H2,1-2H3/b13-10-/t18-/m1/s1
• Isomeric SMILES: CCCCCC[C@H](C/C=C\CCCCCCCC(=O)OC)O
• WGK Germany: 3
• Molecular Weight: 312.49
• Beilstein: 6132055
• Reaxy-Rn: 1728450
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1728450&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Class Fatty Acyls
      • Subclass Fatty alcohols

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Class: Fatty Acyls
• Subclass: Fatty alcohols
• Intermediate Tree Nodes: Not available
• Direct Parent: Fatty alcohols
• Alternative Parents: Fatty acid methyl esters Methyl esters Secondary alcohols Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fatty alcohol - Fatty acid methyl ester - Fatty acid ester - Methyl ester - Secondary alcohol - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as fatty alcohols. These are aliphatic alcohols consisting of a chain of a least six carbon atoms.
• 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.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Air sensitive
• Refractive Index: 1.46
• Flash Point(°C): 209°C
• Molecular Weight: 312.500 g/mol
• XLogP3: 6.100
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 16
• Exact Mass: 312.266 Da
• Monoisotopic Mass: 312.266 Da
• Topological Polar Surface Area: 46.500 Ų
• Heavy Atom Count: 22
• Formal Charge: 0
• Complexity: 274.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 1
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1

References

1. 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).  [PMID:] [10.1039/C9GC03796A]

2. Ting Feng, Haoxian Huang, Ying Xu, Xinyu Che, Mingdong Wang, Xiangyu Tao, Yanbin Feng, Song Xue.  (2025)  Multisite synergistic evolution of oleate hydratase via DCCM and the orthogonal location of distal sites.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:40379171] [10.1016/j.ijbiomac.2025.144001]