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L-treonina - Moligand™, ≥99% , CAS No.72-19-5

CAS: 72-19-5 Cat. No.: T108221 Formula: C4H9NO3 Peso molecolare: 119.13 Beilstein Registry Number: 1721646 Numero EC: 200-774-1
336 Citations COA
L-treonina - Moligand™, ≥99% CAS No(72-19-5) by Aladdin Scientific
Disponibile su ordine
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. ≥99%
Synonyms
H-Thr-OH | L-2-Amino-3-hydroxybutyrate | NSC46701 | CHEBI:16857 | GTPL4785 | L-THREONINE [JAN] | (2S,3R)-rel-2-Amino-3-hydroxybutanoic acid | AKOS015840277 | THREONINE [WHO-DD] | Threonine, L- (8CI) | L-alpha-Amino-beta-hydroxybutyric acid | Threonine, DL
Storage
Room temperature,Desiccated
Shipped In
Normale
★
Size
Germania (EU)
USA*
Price
Qty
100g
T108221-100g
—
2 Disponibile
12,93€
250g
T108221-250g
—
2 Disponibile
16,40€
500g
T108221-500g
—
Disponibile ≥10
24,21€
Enter a quantity for the sizes you want to add.
Bulk / Custom
♡ Lista dei desideri ⇅ Aggiungi al confronto ⎙ Print page
SDS
Safety data
COA
Certificate
DS
Datasheet
SP
Spec sheet
Panoramica Specifications Nomi e identificatori Documentazione Advanced Data Taxonomic Classification Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Domande frequenti e articoli Citations of This Product Calcolatori di soluzioni Recensioni
🧪
Why this grade

Moligand™, ≥99% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Desiccated Ships Normale 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 336 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

La L-treonina è stata utilizzata per la selezione di cellule trasformate. È stata anche utilizzata per studiare gli effetti degli aminoacidi nel promuovere il consumo di cibo in Drosophila melanogaster.

Specifications

Sinonimi
H-Thr-OH | L-2-Amino-3-hydroxybutyrate | NSC46701 | CHEBI:16857 | GTPL4785 | L-THREONINE [JAN] | (2S,3R)-rel-2-Amino-3-hydroxybutanoic acid | AKOS015840277 | THREONINE [WHO-DD] | Threonine, L- (8CI) | L-alpha-Amino-beta-hydroxybutyric acid | Threonine, DL
Specifiche e purezza
Moligand™, ≥99%
Meccanismi biochimici e fisiologici
La L-treonina è considerata un aminoacido essenziale. La L-treonina è coinvolta nella sintesi della mucina, una proteina che favorisce la funzione e l'integrità dell'intestino. La L-treonina è necessaria per il funzionamento del sistema immunitario. È ino
Condizioni di conservazione di stoccaggio
Room temperature,Desiccated
Spedito in
Normale
Grado
Moligand™
Purezza
≥99%
Nomi e identificatori
Pubchem Sid
508810678
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508810678
Sorrisi canonici
CC(C(C(=O)O)N)O
IUPAC Name
(2S,3R)-2-amino-3-hydroxybutanoic acid
InChIKey
AYFVYJQAPQTCCC-GBXIJSLDSA-N
INCHI
1S/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2-,3+/m1/s1
Isomeri SMILES
C[C@H]([C@@H](C(=O)O)N)O
RTECS
XO8590000
Peso molecolare
119.13
Beilstein
1721646
Reaxy-Rn
1098902
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098902&ln=

Documentazione

📋 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
ClasseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids
Direct ParentL-alpha-amino acids
Alternative Parents Short-chain hydroxy acids and derivatives  Beta hydroxy acids and derivatives  Fatty acids and conjugates  Secondary alcohols  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents L-alpha-amino acid - Beta-hydroxy acid - Short-chain hydroxy acid - Hydroxy acid - Fatty acid - Amino acid - Secondary alcohol - Carboxylic acid - Monocarboxylic acid or derivatives - Alcohol - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organic oxide - Primary aliphatic amine - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Amine - Aliphatic acyclic compound
DescrizioneThis 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 Common amino acids
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
F2 Tclin Thrombin (11687 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
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
GABRA1 Tclin GABA receptor alpha-1 subunit (399 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
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
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
HRH3 Tclin Histamine H3 receptor (10389 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
Obiettivi associati (non umani)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc16a10 Monocarboxylate transporter 10 (73 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GAP1 General amino-acid permease GAP1 (481 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc1a5 Amino acid transporter (271 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:

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

58 results found

Lot NumberCertificate TypeDataOggetto
K2218736Certificate of AnalysisSep 04, 2026 T108221
E2626527Certificate of AnalysisMay 15, 2026 T108221
E2626526Certificate of AnalysisMay 15, 2026 T108221
E2626525Certificate of AnalysisMay 15, 2026 T108221
H2617527Certificate of AnalysisMay 15, 2026 T108221
H2617528Certificate of AnalysisMay 15, 2026 T108221
H2617529Certificate of AnalysisMay 15, 2026 T108221
H2617530Certificate of AnalysisMay 15, 2026 T108221
G2515508Certificate of AnalysisJun 25, 2025 T108221
G2515509Certificate of AnalysisJun 25, 2025 T108221
G2515486Certificate of AnalysisJun 25, 2025 T108221
G2515506Certificate of AnalysisJun 25, 2025 T108221
G2515507Certificate of AnalysisJun 25, 2025 T108221
C2630026Certificate of AnalysisJun 25, 2025 T108221
L2412786Certificate of AnalysisNov 28, 2024 T108221
L2412787Certificate of AnalysisNov 28, 2024 T108221
L2412788Certificate of AnalysisNov 28, 2024 T108221
L2412789Certificate of AnalysisNov 28, 2024 T108221
L2412790Certificate of AnalysisNov 28, 2024 T108221
J2429645Certificate of AnalysisOct 19, 2024 T108221
J2429646Certificate of AnalysisOct 19, 2024 T108221
J2429647Certificate of AnalysisOct 19, 2024 T108221
J2429648Certificate of AnalysisOct 19, 2024 T108221
J2424788Certificate of AnalysisJul 27, 2024 T108221
J2424787Certificate of AnalysisJul 27, 2024 T108221
J2424789Certificate of AnalysisJul 27, 2024 T108221
L2508493Certificate of AnalysisJul 22, 2024 T108221
L2508492Certificate of AnalysisJul 22, 2024 T108221
D2508767Certificate of AnalysisJul 22, 2024 T108221
D2508739Certificate of AnalysisJul 22, 2024 T108221
D2508768Certificate of AnalysisJul 22, 2024 T108221
D2424432Certificate of AnalysisApr 16, 2024 T108221
D2424431Certificate of AnalysisApr 16, 2024 T108221
K2407160Certificate of AnalysisApr 16, 2024 T108221
K2407159Certificate of AnalysisApr 16, 2024 T108221
D2424430Certificate of AnalysisApr 16, 2024 T108221
D2424429Certificate of AnalysisApr 16, 2024 T108221
D2424428Certificate of AnalysisApr 16, 2024 T108221
D2422453Certificate of AnalysisMar 22, 2024 T108221
D2422452Certificate of AnalysisMar 22, 2024 T108221
D2409288Certificate of AnalysisMar 22, 2024 T108221
D2409287Certificate of AnalysisMar 21, 2024 T108221
D2409289Certificate of AnalysisMar 21, 2024 T108221
K2218728Certificate of AnalysisAug 23, 2022 T108221
K2218737Certificate of AnalysisAug 23, 2022 T108221
K2218740Certificate of AnalysisAug 23, 2022 T108221
K2218745Certificate of AnalysisAug 23, 2022 T108221
I2402454Certificate of AnalysisAug 23, 2022 T108221
L2313065Certificate of AnalysisAug 23, 2022 T108221
L2327022Certificate of AnalysisAug 23, 2022 T108221
A2417099Certificate of AnalysisAug 23, 2022 T108221
J2311101Certificate of AnalysisJan 22, 2022 T108221
B2223237Certificate of AnalysisJan 22, 2022 T108221
B2223234Certificate of AnalysisJan 22, 2022 T108221
B2223232Certificate of AnalysisJan 22, 2022 T108221
B2223224Certificate of AnalysisJan 22, 2022 T108221
B2223183Certificate of AnalysisJan 22, 2022 T108221
B2223168Certificate of AnalysisJan 22, 2022 T108221
Proprietà chimiche e fisiche
SolubilitàSoluble in water. Insoluble in ethanol, ethyl ether and chloroform.
Rotazione specifica [α]-28 ° (C=6, H2O)
Punto di fusione (°C)256 °C (dec.) (lit.)
Peso molecolare119.120 g/mol
XLogP3-2.900
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count4
Rotatable Bond Count2
Exact Mass119.058 Da
Monoisotopic Mass119.058 Da
Topological Polar Surface Area83.600 Ų
Heavy Atom Count8
Formal Charge0
Complexity93.300
Isotope Atom Count0
Defined Atom Stereocenter Count2
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
Editing sugar chains on therapeutic proteins with glycosidase
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Glycosylation aspartic acid Glycosidase protease dextran
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
AAAs β-Acyloxy Alkenyl Amides
Silicon Reagent-Assisted Peptide Synthesis: Research Progress and Methodological Value of Peptide Bond Formation from Unprotected Substrates
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Peptide synthesis
From Analytical Instrument to Synthetic Platform: A New Strategy for Reconstructing Automated Flow Solid-Phase Peptide Synthesis with Standard Analytical HPLC
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
HPLC Peptide synthesis coupling reagent Analytical Instrument
Methods and Applications for the Determination of Amino Acid Content and Composition
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Amino acids Mass spectrometry High-performance liquid chromatography Derivatization free amino acids total amino acids amino acid composition ninhydrin
Experimental Selection of Burgess Reagent: A Decision Framework for Alcohol Dehydration, Primary Amide/Aldoxime Dehydration, and Oxazoline/Thiazoline Cyclization
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Burgess reagent Dehydration reagent
Formation and Control of Carboxyl- and Hydroxyl-Related Impurities in Peptide Synthesis — Using Asp/Glu and Ser/Thr Residue Side Reactions as Examples
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Peptide synthesis Functional Group Carboxyl group
Analysis of Hydrolyzed Pearl as a Cosmetic Raw Material: Preparation Process, Active Components, and Skincare Formulation Applications
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Hydrolyzed Pearl
How Palmitoyl Pentapeptide-4 Acts on the Skin: From the KTTKS Sequence and Skin Delivery to Collagen Matrix Responses
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
Synthetic lipopeptides
The Combination Logic of Palmitoyl Tripeptide-1 and Palmitoyl Pentapeptide-4: Skin Delivery, Matrix Signaling, and Regulation of Collagen Homeostasis
Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides
Tags:
peptide palmitoyl chain
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