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

Name: L-Threonine - Moligand™, ≥99% , CAS No.72-19-5
SKU: T108221
Availability: InStock

CAS: 72-19-5 Cat. No.: T108221 Summenformel: C₄H₉NO₃ Molekulargewicht: 119.13 Beilstein Registry Number: 1721646 EG-Nummer: 200-774-1

336 Citations COA

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GRADE & PURITY Moligand™ ? ≥99%

Synonyms

Storage

Room temperature,Desiccated

Shipped In

Normal

Übersicht Specifications Namen und Kennungen Documentation Advanced Data Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften FAQs und Artikel Citations of This Product Lösungsrechner Bewertungen

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Why this grade

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

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Storage & shipping

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

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Quality documents

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

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Literature proof

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

Übersicht

L-threonine has been used for the selection of transformed cells. It has also been used to study the effects of amino acids in promoting food consumption in Drosophila melanogaster.

Specifications

Synonyme

Spezifikationen & Reinheit

Moligand™, ≥99%

Biochemische und physiologische Mechanismen

L-Threonine is considered an essential amino acid. L-Threonine is involved in the synthesis of mucin, a protein that supports gut function and integrity. L-Threonine is necessary for the immune system to function. It is also required for O-linked glycosyl

Storage

Room temperature,Desiccated

Verschickt in

Normal

Note

Moligand™

Reinheit

≥99%

Namen und Kennungen

Pubchem Sid

508810678

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508810678

Kanonisches Lächeln

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

Isomere SMILES

C[C@H]([C@@H](C(=O)O)N)O

RTECS

XO8590000

Molekulargewicht

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=

Documentation

📋 Safety Data Sheet (SDS)

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

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✅ 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.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Klasse Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Ebene5 Amino acids and derivatives
        Ebene6 Alpha amino acids and derivatives
        Ebene7 Alpha amino acids
        Ebene8 L-alpha-amino acids

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Klasse	Carboxylic acids and derivatives
Subclass	Amino acids, peptides, and analogues
Intermediate Tree Nodes	Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids
Direct Parent	L-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 Framework	Aliphatic 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
Beschreibung	This 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
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

3D-Struktur

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F2 Tclin Thrombin (11687 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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PGR Tclin Progesterone receptor (8562 Activities)

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CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

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HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)

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ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)

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MAOA Tclin Monoamine oxidase A (11911 Activities)

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DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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ACHE Tclin Acetylcholinesterase (18204 Activities)

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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

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SLC6A2 Tclin Norepinephrine transporter (10102 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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Zugehörige Ziele (nicht menschlich)

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)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Slc1a5 Amino acid transporter (271 Activities)

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Wirkungsmechanismen

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)

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 Number	Certificate Type	Datum	Artikel
K2218736	Certificate of Analysis	Sep 04, 2026	T108221
E2626527	Certificate of Analysis	May 15, 2026	T108221
E2626526	Certificate of Analysis	May 15, 2026	T108221
E2626525	Certificate of Analysis	May 15, 2026	T108221
H2617527	Certificate of Analysis	May 15, 2026	T108221
H2617528	Certificate of Analysis	May 15, 2026	T108221
H2617529	Certificate of Analysis	May 15, 2026	T108221
H2617530	Certificate of Analysis	May 15, 2026	T108221
G2515508	Certificate of Analysis	Jun 25, 2025	T108221
G2515509	Certificate of Analysis	Jun 25, 2025	T108221
G2515486	Certificate of Analysis	Jun 25, 2025	T108221
G2515506	Certificate of Analysis	Jun 25, 2025	T108221
G2515507	Certificate of Analysis	Jun 25, 2025	T108221
C2630026	Certificate of Analysis	Jun 25, 2025	T108221
L2412786	Certificate of Analysis	Nov 28, 2024	T108221
L2412787	Certificate of Analysis	Nov 28, 2024	T108221
L2412788	Certificate of Analysis	Nov 28, 2024	T108221
L2412789	Certificate of Analysis	Nov 28, 2024	T108221
L2412790	Certificate of Analysis	Nov 28, 2024	T108221
J2429645	Certificate of Analysis	Oct 19, 2024	T108221
J2429646	Certificate of Analysis	Oct 19, 2024	T108221
J2429647	Certificate of Analysis	Oct 19, 2024	T108221
J2429648	Certificate of Analysis	Oct 19, 2024	T108221
J2424788	Certificate of Analysis	Jul 27, 2024	T108221
J2424787	Certificate of Analysis	Jul 27, 2024	T108221
J2424789	Certificate of Analysis	Jul 27, 2024	T108221
L2508493	Certificate of Analysis	Jul 22, 2024	T108221
L2508492	Certificate of Analysis	Jul 22, 2024	T108221
D2508767	Certificate of Analysis	Jul 22, 2024	T108221
D2508739	Certificate of Analysis	Jul 22, 2024	T108221
D2508768	Certificate of Analysis	Jul 22, 2024	T108221
D2424432	Certificate of Analysis	Apr 16, 2024	T108221
D2424431	Certificate of Analysis	Apr 16, 2024	T108221
K2407160	Certificate of Analysis	Apr 16, 2024	T108221
K2407159	Certificate of Analysis	Apr 16, 2024	T108221
D2424430	Certificate of Analysis	Apr 16, 2024	T108221
D2424429	Certificate of Analysis	Apr 16, 2024	T108221
D2424428	Certificate of Analysis	Apr 16, 2024	T108221
D2422453	Certificate of Analysis	Mar 22, 2024	T108221
D2422452	Certificate of Analysis	Mar 22, 2024	T108221
D2409288	Certificate of Analysis	Mar 22, 2024	T108221
D2409287	Certificate of Analysis	Mar 21, 2024	T108221
D2409289	Certificate of Analysis	Mar 21, 2024	T108221
K2218728	Certificate of Analysis	Aug 23, 2022	T108221
K2218737	Certificate of Analysis	Aug 23, 2022	T108221
K2218740	Certificate of Analysis	Aug 23, 2022	T108221
K2218745	Certificate of Analysis	Aug 23, 2022	T108221
I2402454	Certificate of Analysis	Aug 23, 2022	T108221
L2313065	Certificate of Analysis	Aug 23, 2022	T108221
L2327022	Certificate of Analysis	Aug 23, 2022	T108221
A2417099	Certificate of Analysis	Aug 23, 2022	T108221
J2311101	Certificate of Analysis	Jan 22, 2022	T108221
B2223237	Certificate of Analysis	Jan 22, 2022	T108221
B2223234	Certificate of Analysis	Jan 22, 2022	T108221
B2223232	Certificate of Analysis	Jan 22, 2022	T108221
B2223224	Certificate of Analysis	Jan 22, 2022	T108221
B2223183	Certificate of Analysis	Jan 22, 2022	T108221
B2223168	Certificate of Analysis	Jan 22, 2022	T108221

Chemische und physikalische Eigenschaften

Löslichkeit	Soluble in water. Insoluble in ethanol, ethyl ether and chloroform.
Spezifische Drehung [α]	-28 ° (C=6, H2O)
Schmelzpunkt (°C)	256 °C (dec.) (lit.)
Molekulargewicht	119.120 g/mol
XLogP3	-2.900
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	2
Exact Mass	119.058 Da
Monoisotopic Mass	119.058 Da
Topological Polar Surface Area	83.600 Å²
Heavy Atom Count	8
Formal Charge	0
Complexity	93.300
Isotope Atom Count	0
Defined Atom Stereocenter Count	2
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

FAQs und Artikel

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β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention

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Silicon Reagent-Assisted Peptide Synthesis: Research Progress and Methodological Value of Peptide Bond Formation from Unprotected Substrates

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Peptide synthesis

From Analytical Instrument to Synthetic Platform: A New Strategy for Reconstructing Automated Flow Solid-Phase Peptide Synthesis with Standard Analytical HPLC

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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

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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

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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

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Peptide synthesis Functional Group Carboxyl group

Analysis of Hydrolyzed Pearl as a Cosmetic Raw Material: Preparation Process, Active Components, and Skincare Formulation Applications

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Hydrolyzed Pearl

How Palmitoyl Pentapeptide-4 Acts on the Skin: From the KTTKS Sequence and Skin Delivery to Collagen Matrix Responses

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The Combination Logic of Palmitoyl Tripeptide-1 and Palmitoyl Pentapeptide-4: Skin Delivery, Matrix Signaling, and Regulation of Collagen Homeostasis

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

Storage & shipping

Quality documents

Literature proof

Übersicht

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Kundenbewertungen

📚 Citations by Application

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Verwandte Produkte

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

Storage & shipping

Quality documents

Literature proof

Übersicht

Specifications

Documentation

📋 Safety Data Sheet (SDS)

✅ Certificate of Analysis (COA)

📊 Datasheet

🔬 Specification Sheet

Advanced Data

Molarity Calculator

Dilution Calculator

Reconstitution Calculator

Kundenbewertungen

📚 Citations by Application

Need help choosing the grade?

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