≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 488196028 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488196028 |
| Sonrisas canónicas | CC(C)(C)OC(=O)CCC(C(=O)O)N |
| IUPAC Name | (2S)-2-amino-5-[(2-methylpropan-2-yl)oxy]-5-oxopentanoic acid |
| InChIKey | OIOAKXPMBIZAHL-LURJTMIESA-N |
| INCHI | 1S/C9H17NO4/c1-9(2,3)14-7(11)5-4-6(10)8(12)13/h6H,4-5,10H2,1-3H3,(H,12,13)/t6-/m0/s1 |
| Isómeros SMILES | CC(C)(C)OC(=O)CC[C@@H](C(=O)O)N |
| WGK Alemania | 3 |
| Peso molecular | 203.24 |
| Beilstein | 2049030 |
| Reaxy-Rn | 2049030 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2049030&ln= |
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 |
| Clase | 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 | L-alpha-amino acids Fatty acid esters Branched fatty acids Dicarboxylic acids and derivatives Quaternary ammonium salts Carboxylic acid salts Carboxylic acid esters Carboxylic acids Organic zwitterions Organic salts Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Glutamic acid or derivatives - Alpha-amino acid - L-alpha-amino acid - Branched fatty acid - Fatty acid ester - Dicarboxylic acid or derivatives - Fatty acyl - Quaternary ammonium salt - Carboxylic acid ester - Carboxylic acid salt - Carboxylic acid - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Amine - Organic salt - Organic zwitterion - Aliphatic acyclic compound |
| Descripción | 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 | Fecha | Articulo |
|---|---|---|---|
 D2628020 | Certificate of Analysis | May 09, 2026 | S135595 |
| F2406044 | Certificate of Analysis | Mar 11, 2026 | S135595 |
| E1528156 | Certificate of Analysis | Mar 02, 2026 | S135595 |
| E2512056 | Certificate of Analysis | May 15, 2025 | S135595 |
| B2318735 | Certificate of Analysis | Apr 18, 2025 | S135595 |
| B2318695 | Certificate of Analysis | Dec 19, 2024 | S135595 |
| B2318692 | Certificate of Analysis | Dec 10, 2024 | S135595 |
| B2318737 | Certificate of Analysis | Dec 10, 2024 | S135595 |
| C2624070 | Certificate of Analysis | Oct 10, 2024 | S135595 |
| J2418579 | Certificate of Analysis | Oct 10, 2024 | S135595 |
| J2418580 | Certificate of Analysis | Oct 10, 2024 | S135595 |
| B2318696 | Certificate of Analysis | Feb 07, 2023 | S135595 |
| G1825142 | Certificate of Analysis | Apr 14, 2022 | S135595 |
| Solubilidad | Sparingly soluble in water; practically insoluble in ethanol or ether. |
|---|---|
| Sensibilidad | Moisture Sensitive；Heat sensitive |
| Rotación específica [α] | 10° (C=1,H2O) |
| Punto de fusión (°C) | 182°C(lit.) |
| Peso molecular | 203.240 g/mol |
| XLogP3 | -2.400 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 6 |
| Exact Mass | 203.116 Da |
| Monoisotopic Mass | 203.116 Da |
| Topological Polar Surface Area | 89.600 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 219.000 |
| 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. Donghui Zhang, Shiqi Liu, Zhihao Cai, Weizhe Luo, Guojian Liu, Runhui Liu. (2023) Facile synthesis of N-phenoxycarbonyl amino acids by a two-phase reaction for direct polymerization. Polymer Chemistry, 15 (2): (97-105). [PMID:] [10.1039/D3PY01031G] |
| 2. Bing Li, Yueming Wu, Wenjing Zhang, Si Zhang, Ning Shao, Weiwei Zhang, Lixin Zhang, Jian Fei, Yidong Dai, Runhui Liu. (2019) Efficient synthesis of amino acid polymers for protein stabilization. Biomaterials Science, 7 (9): (3675-3682). [PMID:31322153] [10.1039/C9BM00484J] |
