Determine the necessary mass, volume, or concentration for preparing a solution.
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10mM in Water for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -80°C Ships Dry ice packs + Cold packs 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 9 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Canonical Smiles | Cl[H].N[C@@H](CCCNC(N)=N)C(O)=O |
|---|---|
| IUPAC Name | (2S)-2-amino-5-(diaminomethylideneamino)pentanoic acid;hydrochloride |
| InChIKey | KWTQSFXGGICVPE-WCCKRBBISA-N |
| INCHI | 1S/C6H14N4O2.ClH/c7-4(5(11)12)2-1-3-10-6(8)9;/h4H,1-3,7H2,(H,11,12)(H4,8,9,10);1H/t4-;/m0./s1 |
| Isomeric SMILES | C(C[C@@H](C(=O)O)N)CN=C(N)N.Cl |
| WGK Germany | 1 |
| Alternate CAS | 15595-35-4 |
| Molecular Weight | 210.66 |
| Beilstein | 6099937 |
| Reaxy-Rn | 3631658 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3631658&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 |
| Class | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids |
| Direct Parent | L-alpha-amino acids |
| Alternative Parents | Fatty acids and conjugates Guanidines Amino acids Propargyl-type 1,3-dipolar organic compounds Monocarboxylic acids and derivatives Carboxylic acids Carboximidamides Organopnictogen compounds Organic oxides Monoalkylamines Hydrochlorides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | L-alpha-amino acid - Fatty acid - Guanidine - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Carboximidamide - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Amine - Hydrochloride - Hydrocarbon derivative - Organic oxide - Primary amine - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Primary aliphatic amine - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. |
| External Descriptors | Not available |
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| Sensitivity | Light sensitive. |
|---|---|
| Specific Rotation[α] | 23 ° (C=8, HCl(1+1)) |
| Melt Point(°C) | 226-230°C |
| Molecular Weight | 210.660 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 5 |
| Exact Mass | 210.088 Da |
| Monoisotopic Mass | 210.088 Da |
| Topological Polar Surface Area | 128.000 Ų |
| Heavy Atom Count | 13 |
| Formal Charge | 0 |
| Complexity | 176.000 |
| 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 | 2 |
| 1. Qiang Zheng, Shuai He, Song-Lin Xu, Meng-Die Ma, Min Fan, Jin-Fang Ge. (2023) Pharmacokinetics and tissue distribution of vigabatrin enantiomers in rats. SAUDI PHARMACEUTICAL JOURNAL, [PMID:38223203] [10.1016/j.jsps.2023.101934] |
| 2. Yanbo Wang, Yongzheng Wang, Jian Chen, Shigenobu Koseki, Qing Yang, Hejun Yu, Linglin Fu. (2021) Screening and preservation application of quorum sensing inhibitors of Pseudomonas fluorescens and Shewanella baltica in seafood products. LWT-FOOD SCIENCE AND TECHNOLOGY, [PMID:] [10.1016/j.lwt.2021.111749] |
| 3. Yalin Ye, Xingli Huo, Zongning Yin. (2021) Protein-protein interactions at high concentrations: Effects of ArgHCl and NaCl on the stability, viscosity and aggregation mechanisms of protein solution. INTERNATIONAL JOURNAL OF PHARMACEUTICS, [PMID:33811966] [10.1016/j.ijpharm.2021.120535] |
| 4. Jie Zhu, Hua Han, Faxue Li, Xueli Wang, Jianyong Yu, Chih-Chang Chu, Dequn Wu. (2018) Self-assembly of amino acid-based random copolymers for antibacterial application and infection treatment as nanocarriers. JOURNAL OF COLLOID AND INTERFACE SCIENCE, [PMID:30690388] [10.1016/j.jcis.2018.12.091] |
| 5. Qiang Zheng, Song-Lin Xu, Xin-Lin Guo, Chuan-Yu Wang, Meng-Die Ma, Jin-Fang Ge. (2025) Effects of melatonin on the pharmacokinetics and amino acid metabolism profile of vigabatrin in rats. TOXICOLOGY AND APPLIED PHARMACOLOGY, [PMID:39884559] [10.1016/j.taap.2025.117247] |
| 6. Wang Jiteng, Zhang Jingyi, Li Xinyu, Xu Hanying Y., Yang Yeshun, Zhang Jiankun, Feng Wenping, Chen Qiang, Dong Fen, Han Tao. (2025) Metabolism of arginine in juvenile largemouth bass (Micropterus salmoides) after oral or intraperitoneal administration of arginine or its substrates. AMINO ACIDS, 57 (1): (1-15). [PMID:39945913] [10.1007/s00726-024-03436-z] |
| 7. Shuangshuang Wan, Wurui Liu, Qian Wu, Kepeng Wang, Yaocheng Li, Peihong Huang, Yu Wu, Yunfei Mu, Yulin Fan, Jun Tao, Jia Yao, Fei Peng, Yu Zou, Lianhui Wang, Zhiyao Yuan, Xianguang Ding. (2024) Nanobiohybrid Extracellular Vesicle Nanoreactor with Improving Metabolical Activity for Biocatalytic Therapy. ACS Nano, [PMID:39536071] [10.1021/acsnano.4c12458] |
| 8. Yingjie Sun, Changheng Li, Xiaofei Deng, Wenjie Li, Xiaoyi Deng, Weiqi Ge, Miaoyuan Shi, Ying Guo, Yanxun V Yu, Hai-bing Zhou, Youngnam N Jin. (2024) Target protein identification in live cells and organisms with a non-diffusive proximity tagging system. eLife, [PMID:39728918] [10.7554/eLife.102667] |
| 9. Cheng Cao, Qi Yang, Liming Chen, Xiuqiang Li, Jiazhuo Gong, Lei Liang, Chaojie Yu, Bingyan Guo, Xueyu Wang, Zhongming Zhao, Yuwei Qiu, Fanglian Yao, Junjie Li, Hong Zhang. (2025) Self-Gelling Hemostatic Powders Driven by Hydrogen Bonding and Electrostatic Interactions with Antibacterial and Antioxidant Properties. Journal of Materials Chemistry B, [PMID:40590133] [10.1039/D5TB00032G] |