41989-07-5

Basic information

• Product Name: METHYL RICINOLEATE
• Synonyms: RICINOLIC ACID METHYL ESTER;RICINOLEIC ACID METHYL ESTER;RECINOLEIC ACID METHYL ESTER;DELTA 9 CIS 12 HYDROXY OCTADECENOIC ACID METHYL ESTER;METHYL RICINOLEATE;METHYL RICINOLATE;METHYL 12-HYDROXY-9-OCTADECENOATE;METHYL 12-HYDROXYOLEATE
• CAS NO: 41989-07-5
• Molecular Formula: C₁₉H₃₆O₃
• Molecular Weight: 312.49
• Mol File: 41989-07-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 412.0±28.0 °C(Predicted)
• Appearance: /
• Density: 0.926±0.06 g/cm3(Predicted)
• Storage Temp.: −20°C
• PKA: 15.10±0.20(Predicted)
• CAS DataBase Reference: METHYL RICINOLEATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL RICINOLEATE(41989-07-5)
• EPA Substance Registry System: METHYL RICINOLEATE(41989-07-5)

Safety Data

• WGK Germany: 3
• F: 8-10-21
• Hazardous Substances Data: 41989-07-5(Hazardous Substances Data)

Usage

Chemical Properties

Colorless liquid. Insoluble in water; soluble in alcohol and ether.Combustible.

Uses

Plasticizer, lubricant, cutting oil additive, wet-ting agent.

Definition

The methyl ester ofricinoleic acid.

Upstream product

• 67-56-1 methanol 
• 141-22-0 Ricinoleic acid 
• 111-71-7 heptanal 
• 111-81-9 Methyl 10-undecenoate 
• 41015-43-4 methyl acetyl ricinoleate 

Downstream Products

• 123-99-9 azelaic acid 
• 111-71-7 heptanal 
• 111-81-9 Methyl 10-undecenoate 
• 1577-55-5 octadec-9-ene-1,12-diol 
• 106-14-9 12-Hydroxystearic acid 
• 6114-39-2 methyl 12-hydroxyoctadecanoate 
• 112-61-8 Methyl stearate 
• 822-10-6 octadeca-9,11-dienoic acid methyl ester 
• 1731-86-8 methyl undecanoate 
• 140-03-4 [R-(Z)]-12-(acetyloxy)-9-octadecenoic acid methyl ester 
• 84799-82-6 (Z)-(S)-12-hydroxyoctadec-9-enoic acid methyl ester 
• 822-10-6 (9Z,11E)-methyl octadeca-9,11-dienoate 
• 112-63-0 Methyl linoleate 
• 822-10-6 methyl cis,cis-9,11-octadecadienoate 

Relevant articles and documents

[1 + 1]-Condensation of 12-Oxo-Derivatives of Ricinoleic Acid Esters with Hydrazine Hydrate on the Route to Macrocycles

The reactivities of the keto analogs of methyl ricinolate and its triglyceride with hydrazine hydrate were studied. The ester was found to be inert, which made it possible to synthesize a macrocyclic azine with a side chain hydrazone moiety from a 12-oxo-derivative.

Cleavage of Esters under Nearly Neutral Conditions at High Pressure. Chemo- and Regioselective Hydrolysis in Organic Solvents

Hydrolysis of esters proceeded at room temperature under high pressure in the presence of iPr2NEt or N-methylmorpholine using CH3CN-H2O (60:1) as the solvent.This very mild procedure enables the smooth hydrolysis of biologically important compounds such as amino esters, aliphatic unsaturated fatty esters, and β-hydroxy esters; no racemization, no isomerization, and no side reactions take place.