Determine the necessary mass, volume, or concentration for preparing a solution.
≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Argon charged,Desiccated 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
A L-lysine derivative used in the preparation of Polylysine, a synthetic, basic poly-α-amino acid. Polylysine inhibited fungal penetration and polyphenol formation in susceptible sweet potatoes infected with C. fimbriata and caused some inhibition of fungal growth, a lessening of the penetration by the fungus, and more callus formation in resistant sweet potatoes. The compound inhibited the infection of tomato cuttings by F. lycopersici but was also toxic to the plants. Polyglutamic acid had no effect on the fungi in vitro.
| Pubchem Sid | 504765140 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504765140 |
| Sonrisas canónicas | C1=CC=C(C=C1)COC(=O)NCCCCC2C(=O)OC(=O)N2 |
| IUPAC Name | benzyl N-[4-[(4S)-2,5-dioxo-1,3-oxazolidin-4-yl]butyl]carbamate |
| InChIKey | HLLIDIRDRPSCHN-LBPRGKRZSA-N |
| INCHI | 1S/C15H18N2O5/c18-13-12(17-15(20)22-13)8-4-5-9-16-14(19)21-10-11-6-2-1-3-7-11/h1-3,6-7,12H,4-5,8-10H2,(H,16,19)(H,17,20)/t12-/m0/s1 |
| Isómeros SMILES | C1=CC=C(C=C1)COC(=O)NCCCC[C@H]2C(=O)OC(=O)N2 |
| Peso molecular | 306.31 |
| Reaxy-Rn | 93651 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=93651&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 | Benzenoids |
| Clase | Benzene and substituted derivatives |
| Subclass | Benzyloxycarbonyls |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzyloxycarbonyls |
| Alternative Parents | Alpha amino acids and derivatives Oxazolidinones Carbamate esters Oxacyclic compounds Monocarboxylic acids and derivatives Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Alpha-amino acid or derivatives - Benzyloxycarbonyl - Oxazolidinone - Oxazolidine - Carbamic acid ester - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Organoheterocyclic compound - Azacycle - Organooxygen compound - Organonitrogen compound - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Aromatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as benzyloxycarbonyls. These are organic compounds containing a carbonyl group substituted with a benzyloxyl group. |
| 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 |
|---|---|---|---|
| Certificate of Analysis | Jun 26, 2026 | N305126 | |
| Certificate of Analysis | Jun 26, 2026 | N305126 | |
| Certificate of Analysis | Jun 26, 2026 | N305126 | |
| Certificate of Analysis | Jun 26, 2026 | N305126 | |
| Certificate of Analysis | Mar 01, 2025 | N305126 | |
| Certificate of Analysis | Mar 01, 2025 | N305126 | |
| Certificate of Analysis | Mar 01, 2025 | N305126 | |
| Certificate of Analysis | Mar 01, 2025 | N305126 | |
| Certificate of Analysis | Mar 01, 2025 | N305126 | |
| Certificate of Analysis | Mar 01, 2025 | N305126 | |
| Certificate of Analysis | Jan 05, 2023 | N305126 | |
| Certificate of Analysis | Jan 05, 2023 | N305126 | |
| Certificate of Analysis | Jan 05, 2023 | N305126 | |
| Certificate of Analysis | Jan 05, 2023 | N305126 | |
| Certificate of Analysis | Jan 05, 2023 | N305126 | |
| Certificate of Analysis | Jan 05, 2023 | N305126 | |
| Certificate of Analysis | Mar 19, 2022 | N305126 | |
| Certificate of Analysis | Mar 19, 2022 | N305126 | |
| Certificate of Analysis | Mar 19, 2022 | N305126 | |
| Certificate of Analysis | Mar 19, 2022 | N305126 | |
| Certificate of Analysis | Mar 19, 2022 | N305126 |
| Sensibilidad | Hygroscopic |
|---|---|
| Peso molecular | 306.310 g/mol |
| XLogP3 | 1.800 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 8 |
| Exact Mass | 306.122 Da |
| Monoisotopic Mass | 306.122 Da |
| Topological Polar Surface Area | 93.700 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 407.000 |
| 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. Huang Ruoxi, Yi Yaxin, Zhang Shiyu, Wang Jiaxin, Yuan Haikuan, Lu Jie. (2025) Folic acid grafted amphiphilic dextran-b-poly(ε-benzyloxycarbonyl- l-lysine) micelles for drug’s pH-responsive release. POLYMER BULLETIN, 83 (1): (31). [PMID:] [10.1007/s00289-025-06092-9] |