≥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 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Boc-Lys-OH (Nα-Boc-L-lysine) can be used as a building block to synthesize:
• A heterotrifunctional peptide-based linker molecule applicable as a bio-labeling reagent.
• Lysine derivatives of azamacrocycle and anthraquinone.
• Boc-Lys(Bn4-DTPA)-OH, a precursor to synthesize diethylene triamine pentaacetic acid (DTPA) containing peptides.
• A ferrocene-amino acid conjugate which is used in developing chemical warfare agent (CWA) senso.
| Pubchem Sid | 504760986 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504760986 |
| Kanonisches Lächeln | CC(C)(C)OC(=O)NC(CCCCN)C(=O)O |
| IUPAC Name | (2S)-6-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid |
| InChIKey | DQUHYEDEGRNAFO-QMMMGPOBSA-N |
| INCHI | 1S/C11H22N2O4/c1-11(2,3)17-10(16)13-8(9(14)15)6-4-5-7-12/h8H,4-7,12H2,1-3H3,(H,13,16)(H,14,15)/t8-/m0/s1 |
| Isomere SMILES | CC(C)(C)OC(=O)N[C@@H](CCCCN)C(=O)O |
| WGK Deutschland | 3 |
| Molekulargewicht | 246.3 |
| Beilstein | 4252546 |
| Reaxy-Rn | 2274643 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2274643&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 |
| Klasse | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives |
| Direct Parent | Alpha amino acids and derivatives |
| Alternative Parents | Medium-chain fatty acids Branched fatty acids Amino fatty acids Carbamate esters Organic carbonic acids and derivatives Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Alpha-amino acid or derivatives - Medium-chain fatty acid - Amino fatty acid - Branched fatty acid - Fatty acyl - Fatty acid - Carbamic acid ester - Amino acid - Carbonic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Primary amine - Hydrocarbon derivative - Primary aliphatic amine - Organic oxide - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Amine - Aliphatic acyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. |
| 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 |
|---|---|---|---|
 L2208489 | Certificate of Analysis | Aug 12, 2026 | B110966 |
| L2208539 | Certificate of Analysis | Aug 12, 2026 | B110966 |
| L2208544 | Certificate of Analysis | Aug 12, 2026 | B110966 |
| L2208551 | Certificate of Analysis | Aug 12, 2026 | B110966 |
| C2627150 | Certificate of Analysis | Apr 08, 2026 | B110966 |
| K2120032 | Certificate of Analysis | Sep 04, 2025 | B110966 |
| K2120033 | Certificate of Analysis | Sep 04, 2025 | B110966 |
| K2120217 | Certificate of Analysis | Sep 04, 2025 | B110966 |
| K1701107 | Certificate of Analysis | Jun 12, 2025 | B110966 |
| F2130068 | Certificate of Analysis | Apr 03, 2025 | B110966 |
| F2421130 | Certificate of Analysis | Apr 01, 2024 | B110966 |
| F2629007 | Certificate of Analysis | Oct 21, 2022 | B110966 |
| L2411289 | Certificate of Analysis | Oct 21, 2022 | B110966 |
| C2224014 | Certificate of Analysis | Oct 28, 2021 | B110966 |
| I2319064 | Certificate of Analysis | Oct 28, 2021 | B110966 |
| L2411252 | Certificate of Analysis | Oct 28, 2021 | B110966 |
| Löslichkeit | Soluble in water. Slightly soluble in methanol. |
|---|---|
| Empfindlichkeit | Heat sensitive |
| Spezifische Drehung [α] | 21.5 ° (C=2, MeOH) |
| Schmelzpunkt (°C) | 205°C |
| Molekulargewicht | 246.300 g/mol |
| XLogP3 | -1.600 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 8 |
| Exact Mass | 246.158 Da |
| Monoisotopic Mass | 246.158 Da |
| Topological Polar Surface Area | 102.000 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 261.000 |
| 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. Shan Li, Haifeng Wu, Yuanxi Liu, Baoli Zhang, Shichao Xu, Zhen-Gang Wang. (2023) Oxidase-Mimetic Nanocatalyst Based on Geometry-Dependent Biomolecular Self-Assembly. CHEMISTRY OF MATERIALS, [PMID:] [10.1021/acs.chemmater.3c02028] |
| 2. Zhanpeng Ren, Jianying Wang, Chenglong Xue, Minghua Deng, Haiyang Yu, Tianci Lin, Jiayuan Zheng, Rongxiang He, Xianbao Wang, Jinhua Li. (2023) Ultrahighly Sensitive and Selective Glutathione Sensor Based on Carbon Dot-Functionalized Solution-Gate Graphene Transistor. ANALYTICAL CHEMISTRY, [PMID:37971943] [10.1021/acs.analchem.3c03656] |
| 3. Guoyang Qin, Cong Hu, Yanfen Jiang, Shuqi Dong, Li Liu, Hanying Zhao. (2021) pH/enzyme/light triple-responsive vesicles from lysine-based amphiphilic diblock copolymers. JOURNAL OF POLYMER SCIENCE, 59 (17): (1958-1971). [PMID:] [10.1002/pol.20210245] |
| 4. Shichao Xu, Haifeng Wu, Yuanxi Liu, Zhen-Gang Wang. (2024) Self-Assembled G-fold DNA/Amino Acid Amphiphiles-Based Oxidase-Mimetic Materials Exhibiting Drug-Degrading and Photoswitchable Capabilities. CHEMISTRY OF MATERIALS, [PMID:] [10.1021/acs.chemmater.3c03281] |
| 5. Lin Yi, Li Mengyao, Luo Zijin, Meng Yanan, Zong Yan, Ren Hongyu, Yu Xiaolu, Tan Xiaoqiong, Liu Fan, Wei Tuo, Cheng Qiang. (2025) Tissue-specific mRNA delivery and prime editing with peptide–ionizable lipid nanoparticles. NATURE MATERIALS, [PMID:40890498] [10.1038/s41563-025-02320-9] |
| 6. Qiu Wang, Yi Lin, Zijin Luo, Jiahui Xiao, Keqing Xu, Xiaolu Yu, Yanan Meng, Mengyao Li, Hongyu Ren, Fan Liu, Xiaoqiong Tan, Han Wen, Tuo Wei, Qiang Cheng. (2025) Hydrogen Bond-Assisted Two-Component Lipid Nanoparticles for Spleen-Specific mRNA Delivery. Journal of the American Chemical Society, [PMID:41208607] [10.1021/jacs.5c14194] |
| 7. Qiu Wang, Yi Lin, Jiahui Xiao, Keqing Xu, Zijin Luo, Hongyu Ren, Fan Liu, Lu Jia, Tuo Wei, Qiang Cheng. (2026) Optimizing Peptide Ionizable Lipids Enables Efficient and Low-Toxicity mRNA Delivery for In Vivo Prime Editing and Protein Replacement Therapy. ADVANCED MATERIALS, [PMID:41656866] [10.1002/adma.202522552] |
