1-PALMITOYL-2-OLEOYL-SN-GLYCERO-3-PHOSPHOCHOLINE [26853-31-6]
Referência AG00BBPG-1g
Tamanho : 1g
Marca : Angene
3,5,8-Trioxa-4-phosphahexacos-17-en-1-aminium,4-hydroxy-N,N,N-trimethyl-9-oxo-7-[[(1-oxohexadecyl)oxy]methyl]-, innersalt, 4-oxide, (7R,17Z)-
CCCCCCC/C=CCCCCCCCC)COP(=O)(OCC[N+](C)(C)C)[O-]](/proxy_img/aHR0cHM6Ly9pbWcuYW5nZW5lY2hlbWljYWwuY29tL3N0b3JhZ2UvYWE0NC9hYTQ0MDFjMDY0NTFhYjAzMTc0NDk1ZGVmNjA2ZWE1Yi5wbmc=.png)
| Chemical Name: | 3,5,8-Trioxa-4-phosphahexacos-17-en-1-aminium,4-hydroxy-N,N,N-trimethyl-9-oxo-7-[[(1-oxohexadecyl)oxy]methyl]-, innersalt, 4-oxide, (7R,17Z)- |
| CAS Number: | 26853-31-6 |
| Product Number: | AG00BBPG(AGN-PC-0R2S04) |
| Synonyms: | |
| MDL No: | MFCD00043212 |
| Molecular Formula: | C42H82NO8P |
| Molecular Weight: | 760.0761 |
Identification/Properties
Properties
MP:
>185°C (dec.)
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
760.091g/mol
XLogP3:
13.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
41
Exact Mass:
759.578g/mol
Monoisotopic Mass:
759.578g/mol
Topological Polar Surface Area:
111A^2
Heavy Atom Count:
52
Formal Charge:
0
Complexity:
899
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes
Safety Information
GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A
NMR Spectrum
Other Analytical Data
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Customer Feedback
1-Hexadecanoyl-2-(9Z-octadecenoyl)-sn-glycero-3-phosphocholine, a phospholipid derivative, serves as a crucial building block in chemical synthesis processes. This compound is utilized for its unique structural features and functional properties in various chemical reactions and formulations. In chemical synthesis, 1-Hexadecanoyl-2-(9Z-octadecenoyl)-sn-glycero-3-phosphocholine plays a pivotal role as a key intermediate, facilitating the creation of novel molecules and compounds. Its specific chemical structure enables it to participate effectively in esterification, transesterification, and other synthetic transformations, thus contributing to the development of diverse chemical products and materials. Additionally, the presence of the phosphocholine moiety imparts desirable characteristics to the synthesized compounds, making them suitable for a wide range of applications in pharmaceuticals, cosmetics, and other industries.