1-Moristristin

• CAS: 589-68-4
• Catalog Number: ACM589684
• Category: Glycerides
• Molecular Weight: 302.45
• Molecular Formula: C17H34O4
• Synonyms: 1-Monomyristate Glycerol
• IUPAC Name: 2,3-dihydroxypropyl tetradecanoate
• SMILES: CCCCCCCCCCCCCC(=O)OCC(CO)O
• InChI: InChI=1S/C17H34O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-17(20)21-15-16(19)14-18/h16,18-19H,2-15H2,1H3
• InChI Key: DCBSHORRWZKAKO-UHFFFAOYSA-N
• Melting Point: 67.3 °C
• Appearance: White solid
• Application: 1-Moristristin is a versatile 1-monoglyceride of myristic acid, primarily developed for creating nonionic surfactant micelles. Alongside its surfactant applications, it demonstrates significant antibacterial properties against various Gram-positive bacteria, including Staphylococcus aureus, and exhibits antifungal activity against Candida albicans. Furthermore, 1-Moristristin inhibits the hydrolysis of 2-oleoylglycerol and fatty acid amide hydrolase (FAAH) activity, making it a valuable compound not only in microbiological contexts but also as an important biochemical tool.
• Storage: Freezer
• CNo Chain: C14:0
• Complexity: 231
• Covalently-Bonded Unit Count: 1
• EC Number: 248-329-0
• Exact Mass: 302.24571g/mol
• Formal Charge: 0
• Glyceride: Monomyristin
• H-Bond Acceptor: 4
• H-Bond Donor: 2
• Heavy Atom Count: 21
• Monoisotopic Mass: 302.24571g/mol
• NSC Number: 404225
• Physical State: White solid
• Rotatable Bond Count: 16
• XLogP3: 5.2

Synthetic Use

Upstream Synthesis Route 1

• 13429-27-1

• 589-68-4

Reference: [1]Krafft
[Chemische Berichte, 1903, vol. 36, p. 4341]
Izar
[Biochemische Zeitschrift, 1914, vol. 60, p. 325]

Upstream Synthesis Route 2

• 13429-27-1
• 96-24-2

• 589-68-4

Reference: [1]Krafft
[Chemische Berichte, 1903, vol. 36, p. 4341]

Downstream Synthesis Route 1

• 589-68-4
• 4426-47-5

• 18885-80-8

Reference: [1]Brooks,C.J.W.; Watson,J.
[Chemical Communications (London), 1967, p. 952 - 953]

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