1. Home
  2. 9,12-Octadecadienoic acid (9Z,12Z)-,2-hydroxy-3-[(1-oxohexadecyl)oxy]propyl ester

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

9,12-Octadecadienoic acid (9Z,12Z)-,2-hydroxy-3-[(1-oxohexadecyl)oxy]propyl ester

CCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCC/C=CC/C=CCCCCC)O Request for Quotation
Chemical Name: 9,12-Octadecadienoic acid (9Z,12Z)-,2-hydroxy-3-[(1-oxohexadecyl)oxy]propyl ester
CAS Number: 99032-71-0
Product Number: AG01E9FL(AGN-PC-0W8VYB)
Synonyms:
MDL No:
Molecular Formula: C37H68O5
Molecular Weight: 592.93282

Identification/Properties

Computed Properties
Molecular Weight:
592.946g/mol
XLogP3:
13.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
34
Exact Mass:
592.507g/mol
Monoisotopic Mass:
592.507g/mol
Topological Polar Surface Area:
72.8A^2
Heavy Atom Count:
42
Formal Charge:
0
Complexity:
642
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
2
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


1-Linoleoyl-3-palmitoyl-rac-glycerol, also known as $name$, serves as a versatile building block in chemical synthesis processes. This compound plays a crucial role in the creation of lipid-based molecules, particularly in the formulation of cosmetics and pharmaceuticals. Its unique structure consisting of linoleoyl and palmitoyl groups attached to a glycerol backbone enables it to be utilized in the development of novel drug delivery systems, emulsifiers, and surfactants. In chemical synthesis, $name$ is valued for its ability to enhance solubility and stability of active ingredients, thereby improving the overall efficacy of the final product. Additionally, its biocompatible nature makes it a preferred choice for formulating lipid nanoparticles and microemulsions, which are extensively studied for their applications in targeted drug delivery and encapsulation of bioactive compounds. Furthermore, the incorporation of 1-Linoleoyl-3-palmitoyl-rac-glycerol in chemical reactions facilitates the modification of its lipid chains, offering opportunities for the customization of its properties to suit specific application requirements.