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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)-

Hexadecanoic acid, (1S)-1-(hydroxymethyl)-1,2-ethanediyl ester

CCCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCC)CO Request for Quotation
Chemical Name: Hexadecanoic acid, (1S)-1-(hydroxymethyl)-1,2-ethanediyl ester
CAS Number: 30334-71-5
Product Number: AG00JKJ1(AGN-PC-0R5PYB)
Synonyms:
MDL No:
Molecular Formula: C35H68O5
Molecular Weight: 568.9114

Identification/Properties

Computed Properties
Molecular Weight:
568.924g/mol
XLogP3:
14
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
34
Exact Mass:
568.507g/mol
Monoisotopic Mass:
568.507g/mol
Topological Polar Surface Area:
72.8A^2
Heavy Atom Count:
40
Formal Charge:
0
Complexity:
536
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,2-Dipalmitoyl-sn-glycerol, also known as DPPG, plays a crucial role in chemical synthesis as a versatile building block for the creation of various lipids and lipid-based materials. This compound is commonly used in the production of liposomes, which are spherical vesicles composed of lipid bilayers. Liposomes are valued for their ability to encapsulate and deliver a wide range of active compounds, such as drugs or DNA, making them highly relevant in pharmaceutical and biomedical applications. DPPG can be incorporated into liposome formulations to modify their stability, permeability, and interaction with biological membranes. Additionally, DPPG can be employed in the synthesis of lipid-based nanoparticles and surfactants, contributing to the development of novel drug delivery systems and functional materials. Its unique properties and compatibility with biological systems make DPPG a valuable tool for researchers and chemists in the field of nanotechnology and drug delivery.