L-Isoleucine - Moligand™, 10mM in Water , CAS No.73-32-5

CAS: 73-32-5 Cat. No.: L425728 Formula: C6H13NO2 Peso molecolare: 131.18 Beilstein Registry Number: 4454 Numero EC: 200-798-2
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. 10mM in Water
Synonyms
l-isoleucine|Isoleucine|73-32-5|(2S,3S)-2-Amino-3-methylpentanoic acid|2S,3S-Isoleucine|(S)-Isoleucine|H-Ile-OH|(S,S)-Isoleucine|2-Amino-3-methylvaleric acid|L-(+)-Isoleucine|erythro-L-Isoleucine|L-Ile|ISOLEUCINE, L-|alpha-Amino-beta-methylvaleric acid|Is
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Size
Germania (EU)
USA*
Price
Qty
1ml
L425728-1ml
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2 Disponibile

21,61€

32,02€
Salva 10,41 € (32.52%)
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Why this grade

Moligand™, 10mM in Water Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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 95 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

L-Isoleucine is an essential amino acid used as a supplement in sports nutrition.[1] It is one of the free-amino acids found in common buckwheat.

Specifications

Sinonimi
l-isoleucine | Isoleucine | 73-32-5 | (2S,3S)-2-Amino-3-methylpentanoic acid | 2S,3S-Isoleucine | (S)-Isoleucine | H-Ile-OH | (S,S)-Isoleucine | 2-Amino-3-methylvaleric acid | L-(+)-Isoleucine | erythro-L-Isoleucine | L-Ile | ISOLEUCINE, L- | alpha-Amino-beta-methylvaleric acid | Is
Specifiche e purezza
Moligand™, 10mM in Water
Condizioni di conservazione di stoccaggio
Store at -80°C
Spedito in
Dry ice packs + Cold packs
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Grado
Moligand™
Nomi e identificatori
Pubchem Sid
Sorrisi canonici
CC[C@H](C)[C@@H](C(=O)O)N
IUPAC Name
(2S,3S)-2-amino-3-methylpentanoic acid
InChIKey
AGPKZVBTJJNPAG-WHFBIAKZSA-N
INCHI
1S/C6H13NO2/c1-3-4(2)5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t4-,5-/m0/s1
Isomeri SMILES
CC[C@H](C)[C@@H](C(=O)O)N
RTECS
NR4705000
Peso molecolare
131.18
Beilstein
4454
Reaxy-Rn
1721790
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1721790&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
Direct ParentIsoleucine and derivatives
Alternative Parents L-alpha-amino acids  Methyl-branched fatty acids  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Isoleucine or derivatives - Alpha-amino acid - L-alpha-amino acid - Branched fatty acid - Methyl-branched fatty acid - Fatty acid - Fatty acyl - Amino acid - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxide - Organopnictogen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - 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 isoleucine and derivatives. These are compounds containing isoleucine or a derivative thereof resulting from reaction of isoleucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Amino fatty acids
Struttura 3D
Modello di struttura chimica interattiva





Obiettivi associati (umani)
SLC7A5 Tchem L-type amino acid transporter 1 (388 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC36A1 Tchem Proton-coupled amino acid transporter 1 (102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Obiettivi associati (non umani)
Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc16a10 Monocarboxylate transporter 10 (73 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.

1 results found

Lot NumberCertificate TypeDataOggetto
C2308549Certificate of AnalysisOct 13, 2026 L425728
Proprietà chimiche e fisiche
Rotazione specifica [α]40.5 ° (C=4, 6mol/L HCl)
Punto di fusione (°C)288 °C
Peso molecolare131.170 g/mol
XLogP3-1.700
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count3
Exact Mass131.095 Da
Monoisotopic Mass131.095 Da
Topological Polar Surface Area63.300 Ų
Heavy Atom Count9
Formal Charge0
Complexity103.000
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
List of Natural Amino Acids
Peptide Basics
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
Reassessing Trimethylaluminum: Method Design and Experimental Value of One-Pot Peptide Elongation from Unprotected Amino Acids
Methods and Applications for the Determination of Amino Acid Content and Composition
Analysis of Hydrolyzed Pearl as a Cosmetic Raw Material: Preparation Process, Active Components, and Skincare Formulation Applications
Sources, Host-Regulatory Mechanisms, and Tumor-Immune Effects of Gut Microbiota-Derived Metabolites
Citations of This Product
Calcolatori di soluzioni
Recensioni

Recensioni dei clienti

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