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291129

Sigma-Aldrich

L-Ascorbic acid 6-palmitate

95%

Synonym(s):

6-O-Palmitoyl-L-ascorbic acid, L-Ascorbyl palmitate, Ascorbic acid 6-palmitate

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About This Item

Empirical Formula (Hill Notation):
C22H38O7
CAS Number:
Molecular Weight:
414.53
Beilstein:
96552
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

Assay

95%

optical activity

[α]20/D +22.9°, c = 2 in methanol

mp

115-118 °C (lit.)

SMILES string

[H][C@@]1(OC(=O)C(O)=C1O)[C@@H](O)COC(=O)CCCCCCCCCCCCCCC

InChI

1S/C22H38O7/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-18(24)28-16-17(23)21-19(25)20(26)22(27)29-21/h17,21,23,25-26H,2-16H2,1H3/t17-,21+/m0/s1

InChI key

QAQJMLQRFWZOBN-LAUBAEHRSA-N

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O P Bamidele et al.
Carbohydrate polymers, 216, 217-223 (2019-05-03)
This study determines storage stability and release of encapsulated ascorbyl palmitate in normal and high amylose maize starch by pasting and spray drying. The amount of ascorbyl palmitate released was analysed in the stored samples (dark cupboard, and under UV
Martin Spickenreither et al.
Bioorganic & medicinal chemistry letters, 16(20), 5313-5316 (2006-08-16)
Previously, we identified ascorbic acid 6-O-hexadecanoate as an up to 1500 times more potent inhibitor of bacterial and bovine hyaluronidases than the parent compound, vitamin C, and determined a crystal structure of hyaluronidase from Streptococcus pneumoniae in complex with the
Stephan Braun et al.
European journal of medicinal chemistry, 46(9), 4419-4429 (2011-08-02)
Bacterial hyaluronan lyases (Hyal) degrade hyaluronan, an important component of the extracellular matrix, and are involved in microbial spread. Hyal inhibitors may serve as tools to study the role of the enzyme, its substrates and products in the course of

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