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Palmitic acid - analytical standard,>99%(GC), high purity , CAS No.57-10-3, Agonist of FFA1 receptor

  • analytical standard
  • Moligand™
  • ≥99%(GC)
Item Number
P101058
Grouped product items
SKUSizeAvailabilityPrice Qty
P101058-250mg
250mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$9.90
P101058-5g
5g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$96.90

Basic Description

Synonymspalmitic acid|Hexadecanoic acid|57-10-3|Cetylic acid|palmitate|n-Hexadecanoic acid|Hexadecylic acid|Hydrofol|n-Hexadecoic acid|1-Pentadecanecarboxylic acid|Palmitinic acid|hexaectylic acid|Pentadecanecarboxylic acid|hexadecoic acid|1-Hexyldecanoic Acid|In
Specifications & PurityMoligand™, analytical standard, ≥99%(GC)
Shipped InNormal
Gradeanalytical standard, Moligand™
Action TypeAGONIST
Mechanism of actionAgonist of FFA1 receptor

Associated Targets

ESR1 Tclin Estrogen receptor 0 Activities

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

NR3C1 Tclin Glucocorticoid receptor 0 Activities

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

FABP2 Tchem Fatty acid-binding protein, intestinal 0 Activities

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

GMNN Tbio Geminin 0 Activities

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

PTPN1 Tchem Tyrosine-protein phosphatase non-receptor type 1 0 Activities

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

USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 0 Activities

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

ABCB1 Tchem Multidrug resistance protein 1 0 Activities

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

FABP3 Tchem Fatty acid-binding protein, heart 0 Activities

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

FFAR1 Tchem Free fatty acid receptor 1 0 Activities

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

FABP4 Tchem Fatty acid-binding protein, adipocyte 2 Activities

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

FABP5 Tchem Fatty acid-binding protein 5 2 Activities

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

TLR2 Tchem Toll-like receptor 2 0 Activities

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

SP1 Tbio Transcription factor Sp1 0 Activities

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

RXRA Tclin Retinoic acid receptor RXR-alpha 0 Activities

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

TOP1 Tclin DNA topoisomerase 1 0 Activities

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

TEAD4 Tchem Transcriptional enhancer factor TEF-3 0 Activities

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

TRPV2 Tchem Transient receptor potential cation channel subfamily V member 2 0 Activities

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

RBP4 Tchem Retinol-binding protein 4 0 Activities

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

PTGS1 Tclin Prostaglandin G/H synthase 1 0 Activities

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

PMP22 Tbio Peripheral myelin protein 22 0 Activities

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

PTGS2 Tclin Prostaglandin G/H synthase 2 0 Activities

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

NR1H4 Tclin Bile acid receptor 0 Activities

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

CYP19A1 Tclin Aromatase 0 Activities

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

ACHE Tclin Acetylcholinesterase 0 Activities

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

ALB Tchem Serum albumin 0 Activities

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

AR Tclin Androgen receptor 0 Activities

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

BCHE Tclin Cholinesterase 0 Activities

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

PPARA Tclin Peroxisome proliferator-activated receptor alpha 0 Activities

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

PPARD Tchem Peroxisome proliferator-activated receptor delta 0 Activities

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

PPARG Tclin Peroxisome proliferator-activated receptor gamma 0 Activities

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

OR51E2 Tchem Olfactory receptor 51E2 2 Activities

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

Names and Identifiers

IUPAC Name hexadecanoic acid
INCHI InChI=1S/C16H32O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h2-15H2,1H3,(H,17,18)
InChi Key IPCSVZSSVZVIGE-UHFFFAOYSA-N
Canonical SMILES CCCCCCCCCCCCCCCC(=O)O
Isomeric SMILES CCCCCCCCCCCCCCCC(=O)O
WGK Germany 3
RTECS RT4550000
Alternate CAS 57-10-3
PubChem CID 985
NSC Number 5030
MeSH Entry Terms Acid, Hexadecanoic;Acid, Palmitic;Calcium Palmitate;Hexadecanoic Acid;Palmitate, Calcium;Palmitate, Sodium;Palmitic Acid;Sodium Palmitate
Molecular Weight 256.42
Beilstein 607489
Reaxy-Rn 607489

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

5 results found

Lot NumberCertificate TypeDateItem
J2227530Certificate of AnalysisAug 12, 2024 P101058
J2227580Certificate of AnalysisAug 12, 2024 P101058
I2122233Certificate of AnalysisJun 16, 2023 P101058
E2411027Certificate of AnalysisOct 10, 2022 P101058
K2012128Certificate of AnalysisSep 13, 2022 P101058

Chemical and Physical Properties

SolubilityInsoluble in water, slightly soluble in petroleum ether, soluble in ethanol, easily soluble in ether, chloroform, and glacial acetic acid.
SensitivityMoisture sensitive.
Refractive Index1.4273
Flash Point(°F)235.4 °F
Flash Point(°C)206℃
Boil Point(°C)271.5°C
Melt Point(°C)62°C

Safety and Hazards(GHS)

WGK Germany 3
RTECS RT4550000
Reaxy-Rn 607489
Merck Index 6996

Related Documents

References

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52. Kar-Lok Wong,Yu-Ru Wu,Ka-Shun Cheng,Paul Chan,Chi-Wai Cheung,Dah-Yuu Lu,Tzu-Hui Su,Zhong-Min Liu,Yuk-Man Leung.  (2014-12-03)  Palmitic acid-induced lipotoxicity and protection by (+)-catechin in rat cortical astrocytes..  Pharmacological reports : PR,  66  ((6)): (1106-1113).  [PMID:25443742]
53. Nathalie Nicod,Robert S Parker,Elena Giordano,Virginia Maestro,Alberto Davalos,Francesco Visioli.  (2014-12-04)  Isomer-specific effects of conjugated linoleic acid on HDL functionality associated with reverse cholesterol transport..  The Journal of nutritional biochemistry,  26  ((2)): (165-172).  [PMID:25468613]
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