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L-Ascorbic acid 6-palmitate - 99%, high purity , CAS No.137-66-6

  • ≥99%
Item Number
A104524
Grouped product items
SKUSizeAvailabilityPrice Qty
A104524-25g
25g
Available within 1-2 weeks(?)
Item is derived from our semi-finished stock and is processed in 1-2 weeks.
$19.90
A104524-100g
100g
In stock
$71.90
A104524-250g
250g
In stock
$161.90
A104524-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$290.90
View related series
Chemical Biology Glycoscience

Basic Description

SynonymsASCORBYL PALMITATE|137-66-6|L-Ascorbyl 6-palmitate|6-O-Palmitoyl-L-ascorbic acid|L-Ascorbic acid 6-palmitate|6-O-Palmitoylascorbic acid|L-Ascorbic acid, 6-hexadecanoate|(S)-2-((R)-3,4-Dihydroxy-5-oxo-2,5-dihydrofuran-2-yl)-2-hydroxyethyl palmitate|L-Ascor
Specifications & Purity≥99%
Biochemical and Physiological MechanismsL-Ascorbyl palmitate (Asc-6P) is used along with other fatty acid ascorbates such as L-ascorbyl oleate and L-ascorbyl linoleate to protect cells and membranes from oxidative damage. Fatty acid ascorbate molecules have increased solubility in non-polar (li
Shipped InNormal
Product Description

Product Application:

L-Ascorbyl palmitate (Asc-6P) is used along with other fatty acid ascorbates such as L-ascorbyl oleate and L-ascorbyl linoleate to protect cells and membranes from oxidative damage. Fatty acid ascorbate molecules have increased solubility in non-polar (lipophilic) environments. It is applied as humectants and emollients.

Associated Targets

HSPD1 Tbio 60 kDa heat shock protein, mitochondrial 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TST Tchem Thiosulfate sulfurtransferase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AMY1A Tchem Alpha-amylase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AMY2A Tclin Pancreatic alpha-amylase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HYAL2 Tbio Hyaluronidase-2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

Pubchem Sid488201691
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488201691
IUPAC Name [(2S)-2-[(2R)-3,4-dihydroxy-5-oxo-2H-furan-2-yl]-2-hydroxyethyl] hexadecanoate
INCHI 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
Canonical SMILES CCCCCCCCCCCCCCCC(=O)OCC(C1C(=C(C(=O)O1)O)O)O
Isomeric SMILES CCCCCCCCCCCCCCCC(=O)OC[C@@H]([C@@H]1C(=C(C(=O)O1)O)O)O
WGK Germany 1
PubChem CID 54680660
Molecular Weight 414.53
Beilstein 96552

Certificates

Certificate of Analysis(COA)

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13 results found

Lot NumberCertificate TypeDateItem
G2416551Certificate of AnalysisApr 29, 2024 A104524
G2416552Certificate of AnalysisApr 29, 2024 A104524
G2416554Certificate of AnalysisApr 29, 2024 A104524
H2308688Certificate of AnalysisMay 24, 2023 A104524
H2308690Certificate of AnalysisMay 24, 2023 A104524
H2308691Certificate of AnalysisMay 24, 2023 A104524
H2308693Certificate of AnalysisMay 24, 2023 A104524
B2310303Certificate of AnalysisFeb 16, 2023 A104524
B2219248Certificate of AnalysisFeb 23, 2022 A104524
B2219306Certificate of AnalysisFeb 23, 2022 A104524
B2219316Certificate of AnalysisFeb 23, 2022 A104524
B2219317Certificate of AnalysisFeb 23, 2022 A104524
E2304428Certificate of AnalysisFeb 23, 2022 A104524

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Chemical and Physical Properties

SensitivityLight sensitive.
Specific Rotation[α]22.5 ° (C=1, EtOH)
Melt Point(°C)114°C

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H319:Causes serious eye irritation

H412:Harmful to aquatic life with long lasting effects

Precautionary Statements

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P273:Avoid release to the environment.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P501:Dispose of contents/container to ...

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P337+P317:If eye irritation persists: Get medical help.

WGK Germany 1

Related Documents

References

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2. Karl-Heinz Wagner,Patrick Feigl,Ibrahim Elmadfa.  (2005-04-06)  Ascorbyl palmitate and its synergism to tocopherols..  Forum of nutrition,  56  (347-348).  [PMID:15806929]
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13. Raju Jukanti,Gopinath Devraj,Apte S Shashank,Rambhau Devraj.  (2011-01-27)  Biodistribution of ascorbyl palmitate loaded doxorubicin pegylated liposomes in solid tumor bearing mice..  Journal of microencapsulation,  28  ((2)): (142-149).  [PMID:21265713]
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16. Luciano Benedini,Maria Laura Fanani,Bruno Maggio,Natalia Wilke,Paula Messina,Santiago Palma,Pablo Schulz.  (2011-07-20)  Surface phase behavior and domain topography of ascorbyl palmitate monolayers..  Langmuir : the ACS journal of surfaces and colloids,  27  ((17)): (10914-10919).  [PMID:21766856]
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19. Bente M Jensen,John Sørensen,Grith Mortensen,Martin B Sørensen,Trine K Dalsgaard.  (2011-11-11)  Effect of antioxidants on oxidation during the production of whey fat concentrate..  Journal of agricultural and food chemistry,  59  ((24)): (13012-13017).  [PMID:22070410]
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22. Mi Kyung Kim,Ji-Soo Lee,Kwang Yup Kim,Hyeon Gyu Lee.  (2012-12-19)  Ascorbyl palmitate-loaded chitosan nanoparticles: characteristic and polyphenol oxidase inhibitory activity..  Colloids and surfaces. B, Biointerfaces,  103  (391-394).  [PMID:23247266]
23. Mirjam Gosenca,Marija Bešter-Rogač,Mirjana Gašperlin.  (2013-05-07)  Lecithin based lamellar liquid crystals as a physiologically acceptable dermal delivery system for ascorbyl palmitate..  European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences,  50  ((1)): (114-122).  [PMID:23643736]
24. Li Xiao,Takeki Tsutsui,Nobuhiko Miwa.  (2014-06-06)  The lipophilic vitamin C derivative, 6-o-palmitoylascorbate, protects human lymphocytes, preferentially over ascorbate, against X-ray-induced DNA damage, lipid peroxidation, and protein carbonylation..  Molecular and cellular biochemistry,  394  ((1-2)): (247-259).  [PMID:24898782]
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Solution Calculators