≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
It reacted with 20-methyl spirolide G to form a derivative with a retention time and spectrum identical with the metabolite, 17-O-palmitoyl-20-methyl spirolide G.
It was used in the synthesis of water-soluble N-palmitoyl chitosan (PLCS) by coupling with swollen chitosan in dimethyl sulfoxide (DMSO). It was also used in the synthesis of N-acylphosphatidylserine.
| Pubchem Sid | 488184295 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488184295 |
| Kanonisches Lächeln | CCCCCCCCCCCCCCCC(=O)OC(=O)CCCCCCCCCCCCCCC |
| IUPAC Name | hexadecanoyl hexadecanoate |
| InChIKey | QWZBEFCPZJWDKC-UHFFFAOYSA-N |
| INCHI | 1S/C32H62O3/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31(33)35-32(34)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-30H2,1-2H3 |
| Isomere SMILES | CCCCCCCCCCCCCCCC(=O)OC(=O)CCCCCCCCCCCCCCC |
| WGK Deutschland | 3 |
| PubChem CID | 69339 |
| Molekulargewicht | 494.85 |
| Beilstein | 1807510 |
| Reaxy-Rn | 1807507 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Klasse | Carboxylic acids and derivatives |
| Subclass | Dicarboxylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dicarboxylic acids and derivatives |
| Alternative Parents | Carboxylic acid anhydrides Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Dicarboxylic acid or derivatives - Carboxylic acid anhydride - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Datum | Artikel |
|---|---|---|---|
 B2323305 | Certificate of Analysis | Feb 28, 2023 | P160066 |
| B2323314 | Certificate of Analysis | Feb 28, 2023 | P160066 |
| B2323316 | Certificate of Analysis | Feb 28, 2023 | P160066 |
| B2323273 | Certificate of Analysis | Feb 27, 2023 | P160066 |
| B2323274 | Certificate of Analysis | Feb 27, 2023 | P160066 |
| B2323282 | Certificate of Analysis | Feb 27, 2023 | P160066 |
| B2323306 | Certificate of Analysis | Feb 27, 2023 | P160066 |
| G2529049 | Certificate of Analysis | Feb 27, 2023 | P160066 |
| Empfindlichkeit | Moisture Sensitive |
|---|---|
| Schmelzpunkt (°C) | 64 °C |
| Molekulargewicht | 494.800 g/mol |
| XLogP3 | 14.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 30 |
| Exact Mass | 494.47 Da |
| Monoisotopic Mass | 494.47 Da |
| Topological Polar Surface Area | 43.400 Ų |
| Heavy Atom Count | 35 |
| Formal Charge | 0 |
| Complexity | 406.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Ran Zhang, Xue-Qing Song, Rui-Ping Liu, Zhong-Ying Ma, Jing-Yuan Xu. (2019) Fuplatin: An Efficient and Low-Toxic Dual-Prodrug. JOURNAL OF MEDICINAL CHEMISTRY, [PMID:31002510] [10.1021/acs.jmedchem.9b00128] |
