D-Glutamic acid - Moligand™, ≥98% , CAS No.6893-26-1

CAS: 6893-26-1 Cat. No.: G100444 Peso molecular: 147.13 Beilstein Registry Number: 1723800 Número EC: 230-000-8
Disponible para pedir
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
(r)-1-aminopropane-1,3-dicarboxylic acid | (2R)-2-aminopentanedioate | SR-01000597732 | CHEBI:53375 | GLUTAMIC ACID D-FORM [MI] | C00217 | D-Glutaminic acid | PDSP2_001470 | D-2-Aminoglutaric acid | delta-Glutaminate | D-Glutamic acid, >=99% (TLC) | DB025
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
G100444-5g
5

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
25g
G100444-25g
5

10,90US$

16,90US$
Guardar 6,00 US$ (35.50%)
50g
G100444-50g
2

19,90US$

29,90US$
Guardar 10,00 US$ (33.44%)
100g
G100444-100g
2

34,90US$

52,90US$
Guardar 18,00 US$ (34.03%)
250g
G100444-250g
2

43,90US$

65,90US$
Guardar 22,00 US$ (33.38%)
500g
G100444-500g
1

52,90US$

79,90US$
Guardar 27,00 US$ (33.79%)
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Why this grade

Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 19 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

D-Glutamic acid is an essential constituent of the bacterial peptidoglycan structure. It is added to UDP-N-acetylmuramyl-L-alanine (UDP-MurNAc-L-alanine) by the enzyme D-glutamic acid-adding enzyme (murD). This is, then, incorporated into the peptidoglycan precursor. Peptidoglycan makes up the cell walls of Gram-positive and -negative bacteria. The conversion of L-glutamate to D-glutamate by glutamate racemase (GR) enzyme is an essential step in the synthesis of peptidoglycan.


application:

D-Glutamic acid acts as a superior to alpha ketoglutarate. It helps in the growth of Lactobacillus arabinosus. It can inhibit the IgE binding to peanut allergens. It is widely used in pharmaceuticals and foods.

Specifications

Sinónimos
(r)-1-aminopropane-1, 3-dicarboxylic acid | (2R)-2-aminopentanedioate | SR-01000597732 | CHEBI:53375 | GLUTAMIC ACID D-FORM [MI] | C00217 | D-Glutaminic acid | PDSP2_001470 | D-2-Aminoglutaric acid | delta-Glutaminate | D-Glutamic acid, >=99% (TLC) | DB025
Especificaciones y pureza
Moligand™, ≥98%
Mecanismos bioquímicos y fisiológicos
Excitatory amino acid acting at NMDA receptors; less active than the L-isomer.L-isomeralso available.
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Grado
Moligand™
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488182816
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488182816
Sonrisas canónicasC(CC(=O)O)C(C(=O)O)N
IUPAC Name(2R)-2-aminopentanedioic acid
InChIKeyWHUUTDBJXJRKMK-GSVOUGTGSA-N
INCHI1S/C5H9NO4/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H,7,8)(H,9,10)/t3-/m1/s1
Isómeros SMILES C(CC(=O)O)[C@H](C(=O)O)N
WGK Alemania 1
Peso molecular 147.13
Beilstein 1723800
Reaxy-Rn 1723799
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1723799&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentGlutamic acid and derivatives
Alternative Parents D-alpha-amino acids  Amino fatty acids  Dicarboxylic acids and derivatives  Amino acids  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Glutamic acid or derivatives - Alpha-amino acid - D-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
DescripciónThis 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 Other amino acids
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRM3 Tchem Metabotropic glutamate receptor 3 (732 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRM4 Tchem Metabotropic glutamate receptor 4 (2320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRM6 Tchem Metabotropic glutamate receptor 6 (361 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRM1 Tchem Metabotropic glutamate receptor 1 (2309 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRM5 Tchem Metabotropic glutamate receptor 5 (5733 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC1A3 Tchem Excitatory amino acid transporter 1 (586 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THP-1 (11052 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FTO Tchem Alpha-ketoglutarate-dependent dioxygenase FTO (473 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Grm2 Metabotropic glutamate receptor 2 (1326 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grm7 Metabotropic glutamate receptor 7 (580 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
murI Glutamate racemase (2 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Gria2 Glutamate receptor ionotropic, AMPA (2103 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grik1 Glutamate receptor ionotropic, kainate (722 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

33 results found

Lot NumberCertificate TypeFechaArticulo
E2223106Certificate of AnalysisMar 11, 2026 G100444
H2525511Certificate of AnalysisJun 12, 2025 G100444
H2525510Certificate of AnalysisJun 12, 2025 G100444
H2525509Certificate of AnalysisJun 12, 2025 G100444
H2525508Certificate of AnalysisJun 12, 2025 G100444
H2525367Certificate of AnalysisJun 12, 2025 G100444
L2031127Certificate of AnalysisOct 14, 2024 G100444
I2411359Certificate of AnalysisSep 02, 2024 G100444
I2411358Certificate of AnalysisSep 02, 2024 G100444
I2411357Certificate of AnalysisSep 02, 2024 G100444
I2411355Certificate of AnalysisSep 02, 2024 G100444
I2411356Certificate of AnalysisSep 02, 2024 G100444
E2411269Certificate of AnalysisMar 21, 2024 G100444
G2321286Certificate of AnalysisJun 30, 2023 G100444
G2321350Certificate of AnalysisJun 30, 2023 G100444
G2321358Certificate of AnalysisJun 30, 2023 G100444
G2321365Certificate of AnalysisJun 30, 2023 G100444
G2321381Certificate of AnalysisJun 30, 2023 G100444
G2321382Certificate of AnalysisJun 30, 2023 G100444
G2321427Certificate of AnalysisJun 30, 2023 G100444
C2605165Certificate of AnalysisJun 30, 2023 G100444
J2222326Certificate of AnalysisJul 04, 2022 G100444
B2309083Certificate of AnalysisJul 04, 2022 G100444
J2222328Certificate of AnalysisJul 04, 2022 G100444
J2222345Certificate of AnalysisJul 04, 2022 G100444
J2222354Certificate of AnalysisJul 04, 2022 G100444
J2222358Certificate of AnalysisJul 04, 2022 G100444
J2222325Certificate of AnalysisJul 04, 2022 G100444
D2319408Certificate of AnalysisJul 04, 2022 G100444
F2218030Certificate of AnalysisJun 22, 2022 G100444
E2223102Certificate of AnalysisFeb 26, 2022 G100444
E2223103Certificate of AnalysisFeb 26, 2022 G100444
E2223104Certificate of AnalysisFeb 26, 2022 G100444

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Propiedades químicas y físicas
SolubilidadSoluble in water, slightly soluble in ethanol, insoluble in ether
Rotación específica [α]-30.0 to -33.0 deg(C=5, HCl(1+5))
Punto de fusión (°C)200-202°C
Peso molecular147.130 g/mol
XLogP3-3.700
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass147.053 Da
Monoisotopic Mass147.053 Da
Topological Polar Surface Area101.000 Ų
Heavy Atom Count10
Formal Charge0
Complexity145.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Wang Ting, Zhang Jieyuan, Wu Yue, Wang Shiyi, Jiang Xinhui, Zhang Zhengwei, Li Siqiao.  (2023)  Smartphone-integrated ratiometric fluorescence sensing platform based on bimetallic metal–organic framework nanowires for anthrax biomarker detection.  MICROCHIMICA ACTA,  190  (12): (1-9).  [PMID:38006440] [10.1007/s00604-023-06065-7]
2. Zhou Shiying, Wang Xianfeng, Zhao Peng, Zheng Jilin, Yang Mei, Huo Danqun, Hou Changjun.  (2021)  ZIF-67 MOF-derived Co nanoparticles supported on N-doped carbon skeletons for the amperometric determination of hydrogen peroxide.  MICROCHIMICA ACTA,  188  (11): (1-10).  [PMID:34661751] [10.1007/s00604-021-05020-8]
3. Jinglei Liu, Wenbo Yuan, Caifeng Li, Mengmeng Cheng, Yan Su, Lijian Xu, Tianfei Chu, Shifeng Hou.  (2021)  l-Cysteine-Modified Graphene Oxide-Based Membrane for Chiral Selective Separation.  ACS Applied Materials & Interfaces,      [PMID:34628847] [10.1021/acsami.1c14900]
4. Liu Nijuan, Liu Jingjing, Niu Xiaohui, Wang Jia, Guo Ruibin, Mo Zunli.  (2021)  An electrochemical chiral sensor based on the synergy of chiral ionic liquid and 3D-NGMWCNT for tryptophan enantioselective recognition.  MICROCHIMICA ACTA,  188  (5): (1-13).  [PMID:33839948] [10.1007/s00604-021-04818-w]
5. Fangqin Wang, Wenrong Cai, Lilan Tan, Junyao Li, Datong Wu, Yong Kong.  (2024)  A Liquid–Liquid Interfacial Strategy for Construction of Electroactive Chiral Covalent–Organic Frameworks with the Aim to Enlarge the Testing Scope of Chiral Electroanalysis.  ANALYTICAL CHEMISTRY,      [PMID:38335728] [10.1021/acs.analchem.3c05744]
6. Wenrong Cai, Yanjing Shi, Ning Liu, Zheng-Zhi Yin, Junyao Li, Laidi Xu, Datong Wu, Yong Kong.  (2024)  A photothermal effect-based chiral sensor for chiral discrimination and sensitive detection.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:38788508] [10.1016/j.saa.2024.124494]
7. Jun Zhang, Kai Wu, Xiaoqing Gao, Min Zhang, Xin Zhou, Florian Bertram, Chen Shen, Yunlong Zhou.  (2024)  Achiral and chiral ligands synergistically harness chiral self-assembly of inorganics.  Science Advances,  10  (42):   [PMID:39423258] [10.1126/sciadv.ado5948]
8. Ding Junfeng, Wang Tianran, Lin Zhiqiang, Li Zhenyu, Yang Jiaxuan, Li Fujiang, Rong Yan, Chen Xuesi, He Chaoliang.  (2025)  Chiral polypeptide hydrogels regulating local immune microenvironment and anti-tumor immune response.  Nature Communications,  16  (1): (1-21).  [PMID:39890820] [10.1038/s41467-025-56137-w]
9. Hui Liu, Huiting Xu, Zhaofeng Song, Zhengwen Li, Saiwei Zhang, Yili Zhang, Jixiang Wang, Xiaoyong Qian.  (2025)  Effects of alkaline pretreatment on the distribution of amino acid enantiomers and their biofunctions during the anaerobic digestion of waste activated sludge.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.159334]
10. Shuyun Liu, Hanju Sun, Merga Nagassa, Xinzhou He, Hui Pei, Lingyan Gao, Xiao Li, Shudong He.  (2024)  Enhancing bread anti-staling with glucose-derived Maillard reaction products: In-depth analysis of starches, gluten networks, and moisture status.  FOOD CHEMISTRY,      [PMID:38824734] [10.1016/j.foodchem.2024.139760]
11. Yuxin He, Hanting Wang, Yuting Yan, Xinhui Jiang, Hecun Zou, Zhengwei Zhang.  (2024)  Facile synthesis of nitrogen-doped carbon dots for ultrasensitive detection of anticancer drug gefitinib based on IFE.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:38277783] [10.1016/j.saa.2024.123942]
12. Lilan Tan, Wenrong Cai, Fangqin Wang, Junyao Li, Datong Wu, Yong Kong.  (2024)  Postsynthetic Modification Strategy for Constructing Electrochemiluminescence-Active Chiral Covalent Organic Frameworks Performing Efficient Enantioselective Sensing.  ANALYTICAL CHEMISTRY,      [PMID:38394220] [10.1021/acs.analchem.3c05887]
13. Jieyuan Zhang, Ting Wang, Yuxuan Du, Yue Wu, Xinhui Jiang, Hecun Zou, Zhengwei Zhang.  (2024)  Smartphone-assisted ratiometric fluorescence sensor based on NS-codoped carbon dots/Au nanoclusters for rapid detection of Hg2+.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.110201]
14. Qiaoru Zhang, Yu Wang, Tianyu Song, Mashooq Khan, Yanjun Gong, Yongxian Guo, Qiongzheng Hu.  (2025)  Molecular Structural Transformation from the D–A to D–D’ of an AIEgen for the Highly Sensitive Detection of Hydrogen Peroxide in Exhaled Breath Condensate.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2025.137124]
15. Hongshun Sun, Hongshun Sun, Yunhao Cao, Yunhao Cao, Yusa Chen, Yusa Chen, Liye Li, Liye Li, Lijun Ma, Lijun Ma, Shengxiao Jin, Shengxiao Jin, Guodong Gu, Xubo Song, Wengang Wu, Wengang Wu, Wengang Wu, Wengang Wu, Zhihong Feng.  (2025)  Angle-multiplexed guided mode resonance metasurfaces for broadband terahertz fingerprint detection.  Photonics Research,  13  (11): (3102-3110).  [PMID:] [10.1364/PRJ.572956]
16. Bo Shen, Zhengqiu Chen, Junyu Chen, Ning Wang, Huaming Mao, Jungang Yin, Yu Ren, Wei Dai, Shuanglong Zhao, Hongwei Yang.  (2025)  Pervasive Construction of Cu@Ag Core–Shell Structures Driven by Glutamate Coordination.  CRYSTAL GROWTH & DESIGN,      [PMID:] [10.1021/acs.cgd.5c01031]
17. Huimin Wang, Guangxin Wang, Ruoxi Liu, Jin Yong Lee, Shufeng Liu, Yingqi Tang, Jing Yu.  (2025)  Electrochemiluminescent Enantiodiscrimination on Chiral Engineered l-His-ZIF8.  LANGMUIR,      [PMID:41217085] [10.1021/acs.langmuir.5c03908]
18. Fan Wu, Junyao Li, Ning Gu, Wenxin Huang, Datong Wu, Wenrong Cai, Zheng-Zhi Yin, Yong Kong.  (2026)  A dual-functional sensor for electrochemical discrimination and detection of glucose enantiomers based on chiral Au/Co3O4 nanoclusters.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2026.117002]
19. Simin Zhang, Xiangfeng Chen, Yaping Shi, Xiangyu Zhu, Zongwei Cai.  (2026)  Soft-Chain-Induced Ultrahigh-Resolution Chiral Separation of Amino Acids via Bimetallic Immobilization in MALDI-TIMS-MS.  ANALYTICAL CHEMISTRY,      [PMID:41701523] [10.1021/acs.analchem.5c07869]
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