Acido L(+)-glutammico - ≥99% , CAS No.56-86-0

CAS: 56-86-0 Cat. No.: G103978 Formula: C5H9NO4 Peso molecolare: 147.13 Beilstein Registry Number: 1723801 Numero EC: 200-293-7
Disponibile su ordine
QUALITÀ & PUREZZA ≥99%
Synonyms
DTXCID30659 | glt | 1ii5 | Glutammato, L- | Acido glutammico, (S)- | Glutaton | glutammato | Acido L-Glutaminico | Acido Gamma-L-Glutammico | EC 200-293-7 | Acido L-glutammico | (2S)-2-aminopentandioato | (S)-Acido glutammico | Acido L-alfa-Aminoglutarico
Storage
Room temperature,Desiccated
Shipped In
Normale
★
Dimensione
Germania (EU)
USA*
Prezzo
Qtà
25g
G103978-25g
Su ordinazione · 8–12 settimane
8,59€
100g
G103978-100g
2 Disponibile
Disponibile ≥10
11,19€
250g
G103978-250g
—
5 Disponibile
19,00€
500g
G103978-500g
—
3 Disponibile
29,42€
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Perché questa qualità

≥99% per flussi di lavoro cromatografici e analitici sensibili che richiedono un'interferenza minima della linea di base.

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Stoccaggio e spedizione

Room temperature,Desiccated Spedizione Normale. Consultare il COA specifico del lotto per le specifiche esatte.

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Documenti di qualità

SDS, COA, scheda tecnica e scheda delle specifiche disponibili per il download. COA specifico del lotto accessibile tramite ricerca per numero di lotto.

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Prova documentale

Citato in 49 pubblicazioni peer-reviewed su cromatografia, sintesi organica e reazioni di accoppiamento incrociato.

Specifiche

Sinonimi
DTXCID30659 | glt | 1ii5 | Glutammato, L- | Acido glutammico, (S)- | Glutaton | glutammato | Acido L-Glutaminico | Acido Gamma-L-Glutammico | EC 200-293-7 | Acido L-glutammico | (2S)-2-aminopentandioato | (S)-Acido glutammico | Acido L-alfa-Aminoglutarico
Specifiche e purezza
≥99%
Meccanismi biochimici e fisiologici
Principale neurotrasmettitore eccitatorio. Agisce sui recettori del glutammato. Attivo in vivo.
Condizioni di conservazione di stoccaggio
Room temperature,Desiccated
Spedito in
Normale
Tipo di azione
ACTIVATOR
Nota
Per quanto possibile, si consiglia di preparare e utilizzare le soluzioni lo stesso giorno. Tuttavia, se è necessario preparare in anticipo le soluzioni di riserva, si consiglia di conservarle in aliquote in fiale ben chiuse a -20°C. In genere, queste possono essere utilizzate per un mese. In genere, queste soluzioni sono utilizzabili fino a un mese. Prima dell'uso e dell'apertura della fiala, si consiglia di lasciare che il prodotto si equilibri a temperatura ambiente per almeno 1 ora. Avete bisogno di ulteriori consigli su solubilità, uso e manipolazione? Per ulteriori informazioni, visitare la pagina delle domande frequenti (FAQ).
Purezza
≥99%
Nomi e identificatori
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488183207
Sorrisi canonici
C(CC(=O)O)C(C(=O)O)N
IUPAC Name
(2S)-2-aminopentanedioic acid
InChIKey
WHUUTDBJXJRKMK-VKHMYHEASA-N
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
Isomeri SMILES
C(CC(=O)O)[C@@H](C(=O)O)N
WGK Germania
1
Peso molecolare
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=

Documentazione

📋 Scheda di dati di sicurezza (SDS)

Documento completo su pericoli, manipolazione, stoccaggio e conformità normativa.

<<<<<<< HEAD Scarica SDS → ======= Scarica SDS → >>>>>>> release248-p3

✅ Certificato di analisi (COA)

Dati di qualità specifici del lotto. Inserisci il numero di lotto per recuperare il COA esatto.

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📊 Scheda tecnica

Riepilogo di riferimento rapido delle specifiche e applicazioni del prodotto.

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🔬 Scheda delle specifiche

Attributi di qualità completi e criteri di accettazione per questa qualità.

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Dati avanzati

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClasseCarboxylic 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 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 FrameworkAliphatic 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
DescrizioneThis 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
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
SLC1A1 Tchem Excitatory amino acid transporter 3 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIA4 Tclin Glutamate receptor 4 (5 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIK5 Tclin Glutamate receptor ionotropic, kainate 5 (3 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIK1 Tclin Glutamate receptor ionotropic, kainate 1 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIA2 Tclin Glutamate receptor 2 (5 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIA3 Tclin Glutamate receptor 3 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIK2 Tclin Glutamate receptor ionotropic, kainate 2 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIK3 Tclin Glutamate receptor ionotropic, kainate 3 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRM2 Tchem Metabotropic glutamate receptor 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRM5 Tchem Metabotropic glutamate receptor 5 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRM7 Tchem Metabotropic glutamate receptor 7 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRM8 Tchem Metabotropic glutamate receptor 8 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRIA1 Tclin Glutamate receptor 1 (4 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRM3 Tchem Metabotropic glutamate receptor 3 (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GRM6 Tchem Metabotropic glutamate receptor 6 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
F2 Tclin Thrombin (11687 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FOLH1 Tclin Glutamate carboxypeptidase II (711 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE4A Tclin Phosphodiesterase 4A (1943 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA3 Tchem Adenosine A3 receptor (15931 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
CHAT Tchem Choline acetylase (63 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH3 Tclin Histamine H3 receptor (10389 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIA3 Tclin Glutamate receptor ionotropic, AMPA 3 (127 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDR Tclin Vascular endothelial growth factor receptor 2 (20924 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
GRIA1 Tclin Glutamate receptor ionotropic, AMPA 1 (277 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIA2 Tclin Glutamate receptor ionotropic, AMPA 2 (847 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIK3 Tclin Glutamate receptor ionotropic kainate 3 (50 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
SLC1A1 Tchem Excitatory amino acid transporter 3 (527 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC1A3 Tchem Excitatory amino acid transporter 1 (586 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIK5 Tclin Glutamate receptor ionotropic kainate 5 (45 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACLY Tclin ATP-citrate synthase (168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIK1 Tclin Glutamate receptor ionotropic kainate 1 (340 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GSR Tclin Glutathione reductase (335 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PIN1 Tchem Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (36611 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
tetX Tetanus toxin (50 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc17a1 Renal sodium-dependent phosphate transport protein 1 (33 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grm2 Metabotropic glutamate receptor 2 (1326 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grm8 Metabotropic glutamate receptor 8 (169 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Gria4 Glutamate receptor ionotropic, AMPA 4 (112 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grik2 Glutamate receptor ionotropic kainate 2 (298 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc1a2 Excitatory amino acid transporter 2 (39 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
dapA Dihydrodipicolinate synthase (65 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Canis familiaris (36305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHO (4503 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc1a6 Excitatory amino acid transporter 4 (71 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasma (328 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin1 Glutamate NMDA receptor (6467 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc16a10 Monocarboxylate transporter 10 (73 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
Grin1 Glutamate NMDA receptor; Grin1/Grin2b (1028 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin1 Glutamate receptors; NMDA/AMPA (104 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin1 Glutamate NMDA receptor; Grin1/Grin2a (798 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin1 Glutamate NMDA receptor; Grin1/Grin2c (1127 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Vicia faba (57 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GAP1 General amino-acid permease GAP1 (481 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Gria2 Glutamate receptor AMPA 1/2 (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Carbonic anhydrase-like protein, putative (25 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A085R Prolyl 4-hydroxylase (72 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meccanismi d'azione
Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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98 results found

Lot NumberCertificate TypeDataOggetto
I2602554I2602554Certificate of AnalysisSep 14, 2026 G103978
I2602551I2602551Certificate of AnalysisSep 14, 2026 G103978
I2602549I2602549Certificate of AnalysisSep 14, 2026 G103978
I2602548I2602548Certificate of AnalysisSep 14, 2026 G103978
D2630385D2630385Certificate of AnalysisMay 29, 2026 G103978
D2630390D2630390Certificate of AnalysisMay 08, 2026 G103978
D2630389D2630389Certificate of AnalysisMay 08, 2026 G103978
D2630388D2630388Certificate of AnalysisMay 08, 2026 G103978
D2630383D2630383Certificate of AnalysisMay 08, 2026 G103978
A2621432A2621432Certificate of AnalysisJan 26, 2026 G103978
A2621433A2621433Certificate of AnalysisJan 26, 2026 G103978
A2621439A2621439Certificate of AnalysisJan 26, 2026 G103978
A2621442A2621442Certificate of AnalysisJan 26, 2026 G103978
G2614100G2614100Certificate of AnalysisJan 26, 2026 G103978
A2621443A2621443Certificate of AnalysisJan 26, 2026 G103978
A2621528A2621528Certificate of AnalysisJan 24, 2026 G103978
J2509416J2509416Certificate of AnalysisOct 27, 2025 G103978
J2509414J2509414Certificate of AnalysisOct 17, 2025 G103978
J2509412J2509412Certificate of AnalysisOct 17, 2025 G103978
J2509413J2509413Certificate of AnalysisOct 17, 2025 G103978
J2509415J2509415Certificate of AnalysisOct 17, 2025 G103978
L2523040L2523040Certificate of AnalysisOct 17, 2025 G103978
I2517189I2517189Certificate of AnalysisSep 19, 2025 G103978
F2519763F2519763Certificate of AnalysisJun 27, 2025 G103978
F2519723F2519723Certificate of AnalysisJun 27, 2025 G103978
F2519722F2519722Certificate of AnalysisJun 27, 2025 G103978
F2519721F2519721Certificate of AnalysisJun 27, 2025 G103978
F2519274F2519274Certificate of AnalysisJun 27, 2025 G103978
D2503579D2503579Certificate of AnalysisApr 08, 2025 G103978
D2503528D2503528Certificate of AnalysisApr 08, 2025 G103978
D2503583D2503583Certificate of AnalysisApr 08, 2025 G103978
D2503582D2503582Certificate of AnalysisApr 08, 2025 G103978
D2503271D2503271Certificate of AnalysisApr 08, 2025 G103978
D2503584D2503584Certificate of AnalysisApr 07, 2025 G103978
A2510409A2510409Certificate of AnalysisJan 21, 2025 G103978
A2510410A2510410Certificate of AnalysisJan 14, 2025 G103978
A2510408A2510408Certificate of AnalysisJan 14, 2025 G103978
A2510407A2510407Certificate of AnalysisJan 14, 2025 G103978
A2510317A2510317Certificate of AnalysisJan 14, 2025 G103978
A2510406A2510406Certificate of AnalysisJan 14, 2025 G103978
C2526005C2526005Certificate of AnalysisJan 14, 2025 G103978
L2425367L2425367Certificate of AnalysisDec 26, 2024 G103978
L2425368L2425368Certificate of AnalysisDec 26, 2024 G103978
L2425371L2425371Certificate of AnalysisDec 26, 2024 G103978
L2425491L2425491Certificate of AnalysisDec 26, 2024 G103978
L2425373L2425373Certificate of AnalysisDec 26, 2024 G103978
L2425376L2425376Certificate of AnalysisDec 26, 2024 G103978
I2413063I2413063Certificate of AnalysisJun 17, 2024 G103978
J2414387J2414387Certificate of AnalysisJun 17, 2024 G103978
F2405359F2405359Certificate of AnalysisJun 17, 2024 G103978
F2405363F2405363Certificate of AnalysisJun 17, 2024 G103978
F2405362F2405362Certificate of AnalysisJun 17, 2024 G103978
F2405361F2405361Certificate of AnalysisJun 17, 2024 G103978
F2405360F2405360Certificate of AnalysisJun 17, 2024 G103978
F2405358F2405358Certificate of AnalysisJun 17, 2024 G103978
C2413026C2413026Certificate of AnalysisMar 19, 2024 G103978
C2412033C2412033Certificate of AnalysisMar 14, 2024 G103978
C2414609C2414609Certificate of AnalysisMar 01, 2024 G103978
C2422205C2422205Certificate of AnalysisMar 01, 2024 G103978
C2422193C2422193Certificate of AnalysisMar 01, 2024 G103978
C2421400C2421400Certificate of AnalysisMar 01, 2024 G103978
C2421393C2421393Certificate of AnalysisMar 01, 2024 G103978
B2401107B2401107Certificate of AnalysisFeb 18, 2024 G103978
B2401111B2401111Certificate of AnalysisFeb 18, 2024 G103978
B2401110B2401110Certificate of AnalysisFeb 18, 2024 G103978
B2401108B2401108Certificate of AnalysisFeb 18, 2024 G103978
B2401109B2401109Certificate of AnalysisFeb 02, 2024 G103978
J2320396J2320396Certificate of AnalysisOct 24, 2023 G103978
J2320397J2320397Certificate of AnalysisOct 24, 2023 G103978
J2320419J2320419Certificate of AnalysisOct 24, 2023 G103978
J2307093J2307093Certificate of AnalysisOct 13, 2023 G103978
J2307088J2307088Certificate of AnalysisOct 13, 2023 G103978
L2325075L2325075Certificate of AnalysisOct 13, 2023 G103978
J2307092J2307092Certificate of AnalysisOct 13, 2023 G103978
J2307091J2307091Certificate of AnalysisOct 13, 2023 G103978
J2307090J2307090Certificate of AnalysisOct 13, 2023 G103978
F2329182F2329182Certificate of AnalysisJul 11, 2023 G103978
F2329157F2329157Certificate of AnalysisJul 11, 2023 G103978
F2329156F2329156Certificate of AnalysisJul 11, 2023 G103978
F2329155F2329155Certificate of AnalysisJul 11, 2023 G103978
F2329154F2329154Certificate of AnalysisJul 11, 2023 G103978
D2319517D2319517Certificate of AnalysisApr 25, 2023 G103978
D23191145D23191145Certificate of AnalysisApr 25, 2023 G103978
D23191231D23191231Certificate of AnalysisApr 25, 2023 G103978
D2319463D2319463Certificate of AnalysisApr 25, 2023 G103978
D2319472D2319472Certificate of AnalysisApr 25, 2023 G103978
D2319478D2319478Certificate of AnalysisApr 25, 2023 G103978
I2224396I2224396Certificate of AnalysisSep 30, 2022 G103978
I2224395I2224395Certificate of AnalysisSep 30, 2022 G103978
I2224393I2224393Certificate of AnalysisSep 30, 2022 G103978
I2224383I2224383Certificate of AnalysisSep 30, 2022 G103978
I2224382I2224382Certificate of AnalysisSep 30, 2022 G103978
D2301005D2301005Certificate of AnalysisSep 30, 2022 G103978
B2216308B2216308Certificate of AnalysisFeb 18, 2022 G103978
B2216322B2216322Certificate of AnalysisFeb 18, 2022 G103978
B2216312B2216312Certificate of AnalysisFeb 18, 2022 G103978
B2216328B2216328Certificate of AnalysisFeb 18, 2022 G103978
B2216329B2216329Certificate of AnalysisFeb 18, 2022 G103978
Proprietà chimiche e fisiche
SensibilitàMoisture sensitive.
Rotazione specifica [α]32 ° (C=5, HCl)
Punto di fusione (°C)205°C
Peso molecolare147.130 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
Domande frequenti e articoli
Synthesis and Metabolism of Glutamate and GABA: Core Mechanisms of Neurotransmitters
List of Natural Amino Acids
Bio-based Chemicals: From Platform Molecules to Application Scenarios — Trend Insights and Aladdin’s Product Portfolio
Structure, Function, and Applications of Glutamate Dehydrogenase
Key Enzymes in Amino Acid Metabolism: A Mechanistic Framework and Research Applications
G Protein–Coupled Receptors (GPCRs): Structure, Signaling, and Drug Targets
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
Silicon Reagent-Assisted Peptide Synthesis: Research Progress and Methodological Value of Peptide Bond Formation from Unprotected Substrates
From Analytical Instrument to Synthetic Platform: A New Strategy for Reconstructing Automated Flow Solid-Phase Peptide Synthesis with Standard Analytical HPLC
Neurosteroids and Protective Mechanisms in the Central Nervous System
Molecular Basis of Ferroptosis-Immune Metabolism Crosstalk
Methods and Applications for the Determination of Amino Acid Content and Composition
Porous Graphitic Carbon (PGC) Chromatography Columns: Creating New Selectivity for Challenging Separations through Molecular Shape and the π-Electron Cloud on the Graphitic Surface
What Is Synthetic Biology? The Industrialization Pathway from Upstream Reagent Toolchains to Biomanufacturing Applications
Performance Sources and Formulation Applications of Enzyme-Based Ingredients in Daily Chemical Products: Fermentation Transformation, Enzymatic Reactions, and Application Principles
Analysis of Amino Acid-Based Surfactants: Basic Structure, Performance Origins, Category Selection, and Applications in Personal Care Formulations
Formation and Control of Carboxyl- and Hydroxyl-Related Impurities in Peptide Synthesis — Using Asp/Glu and Ser/Thr Residue Side Reactions as Examples
Neuropathological Mechanisms of Cerebral Infarction
TCA Cycle Metabolite Detection Methods and Result Interpretation
Mechanistic Analysis of Topical Glutathione in Skincare: Cellular Redox Regulation, Skin Delivery Challenges, and SLN-Based Delivery Strategies
Analysis of Hydrolyzed Pearl as a Cosmetic Raw Material: Preparation Process, Active Components, and Skincare Formulation Applications
Moisturizing Mechanism of Polyglutamic Acid: From the γ-Glutamyl Structure to Hydration Networks and Surface Film-Forming Behavior
Mechanisms by Which Fructan-Rich Ophiopogon japonicus Tuberous Root Extract Supports Skin Moisturization and Barrier Function
Structural Characteristics of Ergothioneine, OCTN1-Mediated Uptake by Skin Cells, and Antioxidant Mechanisms
Citations of This Product
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

Domande frequenti

What is the purity of this product?
This product is supplied at ≥99% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.
How should this product be stored?
Store in a cool place, desiccated. Keep the container tightly closed with desiccant — the material is moisture-sensitive.
How is this product shipped?
This product ships under standard ambient conditions. No temperature-controlled packaging is required.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 56-86-0, the molecular formula is C5H9NO4, and the molecular weight is 147.13 g/mol. InChIKey WHUUTDBJXJRKMK-VKHMYHEASA-N.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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