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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
|
G103978-25g
|
25g |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
|
$9.90
|
|
|
G103978-100g
|
100g |
≥10
|
$12.90
|
|
|
G103978-250g
|
250g |
5
|
$21.90
|
|
|
G103978-500g
|
500g |
3
|
$33.90
|
|
Excitatory neurotransmitter
| Synonyms | DTXCID30659 | glt | 1ii5 | Glutamate, L- | Glutamic acid, (S)- | Glutaton | glutamate | L-Glutaminic acid | Gamma-L-Glutamic Acid | EC 200-293-7 | L-glutamic acid | (2S)-2-aminopentanedioate | (S)-Glutamic acid | L-alpha-Aminoglutaric acid | 1ftj | alpha- |
|---|---|
| Specifications & Purity | ≥99% |
| Biochemical and Physiological Mechanisms | Major excitatory neurotransmitter. Acts at glutamate receptors. Active in vivo . |
| Shipped In | Normal |
| Note | Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
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 | L-alpha-amino acids Amino fatty acids Dicarboxylic acids and derivatives Amino acids Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Glutamic acid or derivatives - Alpha-amino acid - L-alpha-amino acid - Amino fatty acid - Dicarboxylic acid or derivatives - Fatty acid - Fatty acyl - Amino acid - Carboxylic acid - Organic oxide - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Amine - Organic nitrogen compound - Hydrocarbon derivative - 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 | Common amino acids - Amino acids |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| Pubchem Sid | 488183207 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488183207 |
| IUPAC Name | (2S)-2-aminopentanedioic acid |
| INCHI | InChI=1S/C5H9NO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H,7,8)(H,9,10)/t3-/m0/s1 |
| InChIKey | WHUUTDBJXJRKMK-VKHMYHEASA-N |
| Smiles | C(CC(=O)O)C(C(=O)O)N |
| Isomeric SMILES | C(CC(=O)O)[C@@H](C(=O)O)N |
| WGK Germany | 1 |
| Molecular Weight | 147.13 |
| Beilstein | 1723801 |
| Reaxy-Rn | 1723799 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1723799&ln= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jun 27, 2025 | G103978 | |
| Certificate of Analysis | Jun 27, 2025 | G103978 | |
| Certificate of Analysis | Jun 27, 2025 | G103978 | |
| Certificate of Analysis | Jun 27, 2025 | G103978 | |
| Certificate of Analysis | Jun 27, 2025 | G103978 | |
| Certificate of Analysis | Apr 08, 2025 | G103978 | |
| Certificate of Analysis | Apr 08, 2025 | G103978 | |
| Certificate of Analysis | Apr 08, 2025 | G103978 | |
| Certificate of Analysis | Apr 08, 2025 | G103978 | |
| Certificate of Analysis | Apr 08, 2025 | G103978 | |
| Certificate of Analysis | Apr 07, 2025 | G103978 | |
| Certificate of Analysis | Jan 21, 2025 | G103978 | |
| Certificate of Analysis | Jan 14, 2025 | G103978 | |
| Certificate of Analysis | Jan 14, 2025 | G103978 | |
| Certificate of Analysis | Jan 14, 2025 | G103978 | |
| Certificate of Analysis | Jan 14, 2025 | G103978 | |
| Certificate of Analysis | Jan 14, 2025 | G103978 | |
| Certificate of Analysis | Jan 14, 2025 | G103978 | |
| Certificate of Analysis | Dec 26, 2024 | G103978 | |
| Certificate of Analysis | Dec 26, 2024 | G103978 | |
| Certificate of Analysis | Dec 26, 2024 | G103978 | |
| Certificate of Analysis | Dec 26, 2024 | G103978 | |
| Certificate of Analysis | Dec 26, 2024 | G103978 | |
| Certificate of Analysis | Dec 26, 2024 | G103978 | |
| Certificate of Analysis | Jun 17, 2024 | G103978 | |
| Certificate of Analysis | Jun 17, 2024 | G103978 | |
| Certificate of Analysis | Jun 17, 2024 | G103978 | |
| Certificate of Analysis | Jun 17, 2024 | G103978 | |
| Certificate of Analysis | Jun 17, 2024 | G103978 | |
| Certificate of Analysis | Jun 17, 2024 | G103978 | |
| Certificate of Analysis | Jun 17, 2024 | G103978 | |
| Certificate of Analysis | Jun 17, 2024 | G103978 | |
| Certificate of Analysis | Mar 19, 2024 | G103978 | |
| Certificate of Analysis | Mar 14, 2024 | G103978 | |
| Certificate of Analysis | Mar 01, 2024 | G103978 | |
| Certificate of Analysis | Mar 01, 2024 | G103978 | |
| Certificate of Analysis | Mar 01, 2024 | G103978 | |
| Certificate of Analysis | Mar 01, 2024 | G103978 | |
| Certificate of Analysis | Mar 01, 2024 | G103978 | |
| Certificate of Analysis | Feb 18, 2024 | G103978 | |
| Certificate of Analysis | Feb 18, 2024 | G103978 | |
| Certificate of Analysis | Feb 18, 2024 | G103978 | |
| Certificate of Analysis | Feb 18, 2024 | G103978 | |
| Certificate of Analysis | Feb 02, 2024 | G103978 | |
| Certificate of Analysis | Oct 24, 2023 | G103978 | |
| Certificate of Analysis | Oct 24, 2023 | G103978 | |
| Certificate of Analysis | Oct 24, 2023 | G103978 | |
| Certificate of Analysis | Oct 13, 2023 | G103978 | |
| Certificate of Analysis | Oct 13, 2023 | G103978 | |
| Certificate of Analysis | Oct 13, 2023 | G103978 | |
| Certificate of Analysis | Oct 13, 2023 | G103978 | |
| Certificate of Analysis | Oct 13, 2023 | G103978 | |
| Certificate of Analysis | Oct 13, 2023 | G103978 | |
| Certificate of Analysis | Jul 11, 2023 | G103978 | |
| Certificate of Analysis | Jul 11, 2023 | G103978 | |
| Certificate of Analysis | Jul 11, 2023 | G103978 | |
| Certificate of Analysis | Jul 11, 2023 | G103978 | |
| Certificate of Analysis | Jul 11, 2023 | G103978 | |
| Certificate of Analysis | Apr 25, 2023 | G103978 | |
| Certificate of Analysis | Apr 25, 2023 | G103978 | |
| Certificate of Analysis | Apr 25, 2023 | G103978 | |
| Certificate of Analysis | Apr 25, 2023 | G103978 | |
| Certificate of Analysis | Apr 25, 2023 | G103978 | |
| Certificate of Analysis | Apr 25, 2023 | G103978 | |
| Certificate of Analysis | Sep 30, 2022 | G103978 | |
| Certificate of Analysis | Sep 30, 2022 | G103978 | |
| Certificate of Analysis | Sep 30, 2022 | G103978 | |
| Certificate of Analysis | Sep 30, 2022 | G103978 | |
| Certificate of Analysis | Sep 30, 2022 | G103978 | |
| Certificate of Analysis | Sep 30, 2022 | G103978 | |
| Certificate of Analysis | Feb 18, 2022 | G103978 | |
| Certificate of Analysis | Feb 18, 2022 | G103978 | |
| Certificate of Analysis | Feb 18, 2022 | G103978 | |
| Certificate of Analysis | Feb 18, 2022 | G103978 | |
| Certificate of Analysis | Feb 18, 2022 | G103978 |
| Sensitivity | Moisture sensitive. |
|---|---|
| Specific Rotation[α] | 32 ° (C=5, HCl) |
| Melt Point(°C) | 205°C |
| Molecular Weight | 147.130 g/mol |
| XLogP3 | -3.700 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 4 |
| Exact Mass | 147.053 Da |
| Monoisotopic Mass | 147.053 Da |
| Topological Polar Surface Area | 101.000 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 145.000 |
| 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 |
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| 20. Jing Zhang, Jing Chen, Jincen Zuo, Jingsha Lan, Zhilin Jiang, Chen Xiao, Xinhui Wang, Yong Zuo. (2025) A novel electrochemical sensor with NiSx@MoS2 composite for efficient NO2− sensing. FOOD CHEMISTRY, 462 (140947). |
| 21. Li Yuhong, Wang Mingshi, Zhang Dong. (2024) An improved method for isotopic and quantitative analysis of dissolved organic carbon in natural water samples. WATER SCIENCE AND TECHNOLOGY, 89 (8): (2060-2072). |
| 22. Huajian Xu, Zhongtao Hu, Zongwei Hao, Changyue Deng, Xiaowen Pi, Binjia Zhang. (2025) Experimental and computational insights into starch pasting as influenced by amino acids with different R-groups. FOOD CHEMISTRY, 465 (141969). |
| 23. Yan Dai, Hao Zhang. (2024) Facile synthesis of copper carbonate analog with peroxidase-like activity for colorimetric detection of isoniazid. Heliyon, 10 |
| 24. Yunyi Liang, Yonghong Luo, Yingji Wu, Xiaona Li, Quyet Van Le, Jianzhang Li, Changlei Xia. (2024) Nucleophilic amino acids as a renewable alternative to petrochemically-derived amines in glycerol epoxy resins. Journal of Bioresources and Bioproducts, |
| 25. Longfei Xu, Ziyi Wang, Kun Du, Zhao Zhao, Jun Tang, Shuaijie Zhang, Zhichao Lu, Yongfeng Luo, Yuanjuan Bai, Jinkang Dou. (2024) Synthesis of glutamic acid-based coordination polymer for dye removal from aqueous solution. JOURNAL OF MOLECULAR LIQUIDS, 395 (123964). |
| 26. Yilin Wang, Ran Wei, Xijing Yang, Jiahao Liang, Xianda Liu, Shengjun Cheng, Shifan Chen, Ziyue Ling, Yujie Xiao, Yuanting Xu, Weifeng Zhao, Changsheng Zhao. (2024) UV-activated “blue bulbs” for photodecomposition and adsorption of bilirubin: Strategic nanoarchitectonics to remove protein-bound toxins. Materials Today, 80 (327). |