L-Threonine - Animal Free, USP, JP, Moligand™, Ph.Eur., for cell culture, ≥99% , CAS No.72-19-5

CAS: 72-19-5 Cat. No.: T108222 Formula: C4H9NO3 Peso molecolare: 119.13 Beilstein Registry Number: 1721646 Numero EC: 200-774-1
Disponibile su ordine
GRADE & PURITY Animal Free ? Animal-free — produced without animal-derived components to reduce contamination risk. Use in biomanufacturing and culture avoiding animal-origin material. USP ? United States Pharmacopeia grade — meets USP monograph specs for pharmaceutical use. Use for drug manufacturing, QC, and applications requiring US compendial compliance. JP ? Japanese Pharmacopoeia grade — conforms to JP monograph standards. Use for pharmaceutical products subject to Japanese regulatory requirements. Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. Ph.Eur. ? European Pharmacopoeia grade — conforms to Ph.Eur. monographs across EU member states. Use for pharmaceutical work needing European compendial compliance. for Cell culture ? Cell-culture grade — low endotoxin and contaminants to support viable cell growth. Use in mammalian/other cell culture media and supplements. ≥99%
Synonyms
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- | bmse000
Storage
Desiccated,Room temperature
Shipped In
Normal
★
Size
Germania (EU)
USA*
Price
Qty
25g
T108222-25g
—
4 Disponibile
106,65€
100g
T108222-100g
—
5 Disponibile
335,73€
500g
T108222-500g
1 Disponibile
1 Disponibile
1.244,25€
Enter a quantity for the sizes you want to add.
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Why this grade

Animal Free, USP, JP, Moligand™, Ph.Eur., for cell culture, ≥99% Animal Free,JP,Moligand™,per la coltura cellulare,Ph.Eur.,USP for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

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

Panoramica

L-Threonine is a naturally occurring amino acid belonging to the aspartate family of amino acids.

Specifications

Sinonimi
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- | bmse000
Specifiche e purezza
Animal Free, USP, JP, Moligand™, Ph.Eur., for cell culture, ≥99%
Meccanismi biochimici e fisiologici
L-Threonine is considered to be an essential amino acid. L-Threonine is involved in the synthesis of mucin, a protein supporting intestinal function and integrity. L-Threonine is required for the performance of the immune system. It is also essential for
Condizioni di conservazione di stoccaggio
Desiccated,Room temperature
Spedito in
Normal
Grado
Animal Free, JP, Moligand™, per la coltura cellulare, Ph.Eur., USP
Purezza
≥99%
Nomi e identificatori
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488180041
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





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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
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SLC6A4 Tclin Serotonin transporter (12625 Activities)
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ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
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OPRM1 Tclin Mu opioid receptor (19785 Activities)
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DRD3 Tclin Dopamine D3 receptor (14368 Activities)
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SLC6A3 Tclin Dopamine transporter (10535 Activities)
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KCNH2 Tclin HERG (29587 Activities)
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PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
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HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)
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TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)
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PDE4A Tclin Phosphodiesterase 4A (1943 Activities)
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ADORA3 Tchem Adenosine A3 receptor (15931 Activities)
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HRH3 Tclin Histamine H3 receptor (10389 Activities)
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KDR Tclin Vascular endothelial growth factor receptor 2 (20924 Activities)
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Obiettivi associati (non umani)
Hdac6 Histone deacetylase 6 (222 Activities)
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Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
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Slc16a10 Monocarboxylate transporter 10 (73 Activities)
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GAP1 General amino-acid permease GAP1 (481 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc1a5 Amino acid transporter (271 Activities)
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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.

14 results found

Lot NumberCertificate TypeDataOggetto
B2210573Certificate of AnalysisJan 07, 2022 T108222
B2210581Certificate of AnalysisJan 07, 2022 T108222
B2210586Certificate of AnalysisJan 07, 2022 T108222
B2311383Certificate of AnalysisJan 07, 2022 T108222
B2311384Certificate of AnalysisJan 07, 2022 T108222
B2524031Certificate of AnalysisJan 07, 2022 T108222
F2307310Certificate of AnalysisJan 07, 2022 T108222
I2512035Certificate of AnalysisJan 07, 2022 T108222
K2222384Certificate of AnalysisJan 07, 2022 T108222
L2405061Certificate of AnalysisJan 07, 2022 T108222
L2420128Certificate of AnalysisJan 07, 2022 T108222
L2502069Certificate of AnalysisJan 07, 2022 T108222
L2511110Certificate of AnalysisJan 07, 2022 T108222
L2519045Certificate of AnalysisJan 07, 2022 T108222
Proprietà chimiche e fisiche
SolubilitàSoluble in water 50 mg/mL.
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
Guidelines For Common Cell Culture Media
From Spec to Bench: Understanding and Using USP Grade Reagents
JP Grade Reagents Explained
For Cell Culture
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
Methods and Applications for the Determination of Amino Acid Content and Composition
Experimental Selection of Burgess Reagent: A Decision Framework for Alcohol Dehydration, Primary Amide/Aldoxime Dehydration, and Oxazoline/Thiazoline Cyclization
Formation and Control of Carboxyl- and Hydroxyl-Related Impurities in Peptide Synthesis — Using Asp/Glu and Ser/Thr Residue Side Reactions as Examples
Analysis of Hydrolyzed Pearl as a Cosmetic Raw Material: Preparation Process, Active Components, and Skincare Formulation Applications
How Palmitoyl Pentapeptide-4 Acts on the Skin: From the KTTKS Sequence and Skin Delivery to Collagen Matrix Responses
The Combination Logic of Palmitoyl Tripeptide-1 and Palmitoyl Pentapeptide-4: Skin Delivery, Matrix Signaling, and Regulation of Collagen Homeostasis
Citations of This Product
Calcolatori di soluzioni
Recensioni

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