cis-9-Octadecenoic Acid methyl ester

• CAS: 112-62-9
• Catalog Number: ACM112629
• Category: Polymer/Macromolecule; Fatty Acids and Ester Homologs
• Molecular Weight: 296.50
• Molecular Formula: C19H36O2
• Synonyms: Methyl cis-9-Octadecenoate
• Boiling Point: 218 °C
• Melting Point: -19°C
• Flash Point: 350°F
• Density: 0.874 (25°C)
• Appearance: Colorless Liquid
• Storage: -20°C
• Alpha Sort: Methyl oleate
• Bond Position Cis Trans: ∆ 9 cis
• CNo.Chain: C18:1
• Compound Derivative: Methyl
• Fatty Acid: 9-Octadecenoic; (Oleic)
• Physical State: Colorless Liquid
• Type: N9,OMEGA 9

Custom Q&A

What is the molecular formula of Methyl oleate?

The molecular formula of Methyl oleate is C19H36O2.

What is the molecular weight of Methyl oleate?

The molecular weight of Methyl oleate is 296.5 g/mol.

What are some synonyms for Methyl oleate?

Some synonyms for Methyl oleate include Oleic acid methyl ester and Methyl cis-9-octadecenoate.

Is Methyl oleate soluble in water?

Methyl oleate is insoluble in water.

What is the IUPAC name of Methyl oleate?

The IUPAC name of Methyl oleate is methyl (Z)-octadec-9-enoate.

What is the InChIKey of Methyl oleate?

The InChIKey of Methyl oleate is QYDYPVFESGNLHU-KHPPLWFESA-N.

How many hydrogen bond acceptor counts does Methyl oleate have?

Methyl oleate has 2 hydrogen bond acceptor counts.

What is the exact mass of Methyl oleate?

The exact mass of Methyl oleate is 296.271530387 g/mol.

What is the Monoisotopic mass of Methyl oleate?

The Monoisotopic mass of Methyl oleate is 296.2.

In which natural products is Methyl oleate found?

Methyl oleate is found in Anchietea pyrifolia and Lepidium meyenii among other organisms.

Synthetic Use

Upstream Synthesis Route 1

• 67-56-1
• 8001-22-7

• 14663-11-7
• 88400-02-6
• 10030-74-7
• 112-62-9
• 112-63-0
• 1120-34-9
• 2733-88-2
• 124-10-7
• 112-39-0
• 1731-92-6
• 112-61-8
• 1120-28-1
• 929-77-1
• 2442-49-1
• 10305-59-6
• 37929-05-8
• 56-81-5

Reference: [1] Patent: WO2007/12190, 2007, A1, . Location in patent: Page/Page column 16-18

Upstream Synthesis Route 2

• 67-56-1

• 14663-11-7
• 88400-02-6
• 10030-74-7
• 112-62-9
• 112-63-0
• 1120-34-9
• 2733-88-2
• 124-10-7
• 112-39-0
• 1731-92-6
• 112-61-8
• 1120-28-1
• 929-77-1
• 2442-49-1
• 10305-59-6
• 37929-05-8
• 56-81-5

Reference: [1] Patent: WO2007/12190, 2007, A1, . Location in patent: Page/Page column 13-15

Upstream Synthesis Route 3

• 67-56-1

• 14663-11-7
• 88400-02-6
• 10030-74-7
• 112-62-9
• 112-63-0
• 1120-34-9
• 2733-88-2
• 124-10-7
• 112-39-0
• 1731-92-6
• 112-61-8
• 1120-28-1
• 929-77-1
• 2442-49-1
• 10305-59-6
• 37929-05-8
• 56-81-5

Reference: [1] Patent: WO2007/12190, 2007, A1, . Location in patent: Page/Page column 10-12

Downstream Synthesis Route 1

• 112-62-9

• 66587-44-8

Reference: [1]Das, Swapan K.; El-Safty, Sherif A.
[ChemCatChem, 2013, vol. 5, # 10, p. 3050 - 3059]

Downstream Synthesis Route 2

• 112-62-9

• 143-28-2

Reference: [1]Current Patent Assignee: PHARMA MAR SA - WO2006/117197, 2006, A1
Location in patent: Page/Page column 14; 20-21

Downstream Synthesis Route 3

• 112-62-9

• 504-54-1

Reference: [1]Sytniczuk, Adrian; Dabrowski, Michał; Banach, Łukasz; Urban, Mateusz; Czarnocka-Śniadała, Sylwia; Milewski, Mariusz; Kajetanowicz, Anna; Grela, Karol
[Journal of the American Chemical Society, 2018, vol. 140, # 28, p. 8895 - 8901]
[2]Current Patent Assignee: UNIVERSITY OF WARSAW - WO2018/197963, 2018, A1
Location in patent: Page/Page column 68
[3]Polonsky; Lederer
[Bulletin de la Societe Chimique de France, 1954, p. 504,509]
[4]McMurry,J.E. et al.
[Journal of Organic Chemistry, 1978, vol. 43, p. 3255 - 3266]

* For details of the synthesis route, please refer to the original source to ensure accuracy.