≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature 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.
| Canonical Smiles | CCCCCCCCCCCC(=O)NC(CCC(=O)O)C(=O)O |
|---|---|
| IUPAC Name | (2S)-2-(dodecanoylamino)pentanedioic acid |
| InChIKey | AVBJHQDHVYGQLS-AWEZNQCLSA-N |
| INCHI | 1S/C17H31NO5/c1-2-3-4-5-6-7-8-9-10-11-15(19)18-14(17(22)23)12-13-16(20)21/h14H,2-13H2,1H3,(H,18,19)(H,20,21)(H,22,23)/t14-/m0/s1 |
| Isomeric SMILES | CCCCCCCCCCCC(=O)N[C@@H](CCC(=O)O)C(=O)O |
| PubChem CID | 93133 |
| Molecular Weight | 329.44 |
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 |
| Class | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives |
| Direct Parent | Glutamic acid and derivatives |
| Alternative Parents | N-acyl-L-alpha-amino acids N-acyl amines Fatty acids and conjugates Dicarboxylic acids and derivatives Secondary carboxylic acid amides Carboxylic acids Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Glutamic acid or derivatives - N-acyl-l-alpha-amino acid - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Dicarboxylic acid or derivatives - Fatty amide - N-acyl-amine - Fatty acyl - Fatty acid - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid - Carbonyl group - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as glutamic acid and derivatives. These are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 D2425291 | Certificate of Analysis | Mar 25, 2024 | L665421 |
| D2425293 | Certificate of Analysis | Mar 25, 2024 | L665421 |
| D2425406 | Certificate of Analysis | Mar 25, 2024 | L665421 |
| D2425408 | Certificate of Analysis | Mar 25, 2024 | L665421 |
| D2425409 | Certificate of Analysis | Mar 25, 2024 | L665421 |
| D2610052 | Certificate of Analysis | Mar 25, 2024 | L665421 |
| H2514120 | Certificate of Analysis | Mar 25, 2024 | L665421 |
| Solubility | DMSO: 4 mg/mL (12.14 mM) |
|---|---|
| Molecular Weight | 329.400 g/mol |
| XLogP3 | 4.200 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 15 |
| Exact Mass | 329.22 Da |
| Monoisotopic Mass | 329.22 Da |
| Topological Polar Surface Area | 104.000 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 357.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| 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. Qingchun Xu, Xiao Liu, Pingxia Guo, Qiang Chen, Gang Liu, Meirong Cai. (2025) Protic Ionic Liquid Additives Achieving Multifunctional Integration of Superior Lubricity, Corrosion Resistance, and Biodegradability. ACS Applied Engineering Materials, [PMID:] [10.1021/acsaenm.5c00266] |
