| Identification | Back Directory | [Name]
L-ALPHA-PALMITIN | [CAS]
32899-41-5 | [Synonyms]
L-α-Palmitin
L-1-MonopalMitin
Einecs 251-283-4
(R)-1-monopalmitin
L-ALPHA-PALMITIN 99+%
1-PalMitoyl-sn-glycerol
(2S)-Glycerol 1-palmitate
3-monopalmitoyl-sn-glycerol
(S)-2,3-Dihydroxypropylpalmitat
[S,(+)]-1-O-Palmitoyl-L-glycerol
(S)-2,3-dihydroxypropyl palmitate
(R)-Glycerol 1-palmitate, L-α-Palmitin
Hexadecanoic Acid (S)-2,3-Dihydroxypropyl Ester
Hexadecanoic Acid (2S)-2,3-Dihydroxypropyl Ester | [EINECS(EC#)]
251-283-4 | [Molecular Formula]
C19H38O4 | [MDL Number]
MFCD29056543 | [MOL File]
32899-41-5.mol | [Molecular Weight]
330.503 |
| Hazard Information | Back Directory | [Uses]
1-Palmitoyl-sn-glycerol is an intermediate in the synthesis of lysophosphatidylcholines and related derivatives as immunomodulators. | [Definition]
ChEBI: 1-hexadecanoyl-sn-glycerol is a 1-acyl-sn-glycerol that has hexadecanoyl (palmitoyl) as the 1-acyl group. It is a 1-acyl-sn-glycerol, a 1-monopalmitoylglycerol and a monoacylglycerol 16:0. It is an enantiomer of a 3-palmitoyl-sn-glycerol. | [Purification Methods]
The stable -form is obtained by crystallisation from EtOH or Skellysolve B, and recrystallisation from Et2O provides the '-form. The -form is obtained on cooling the melt. [Malkin & el Sharbagy J Chem Soc 1631 1936, Chapman J Chem Soc 58 1956, Luton & Jackson J Am Chem Soc 70 2446 1948, Beilstein 2 III 966.] |
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Cool Pharm, Ltd
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