L-Isoleucine - Moligand™, ≥99% , CAS No.73-32-5

CAS: 73-32-5 Cat. No.: I103488 Molecular Weight: 131.18 Beilstein Registry Number: 4454 EC Number: 200-798-2
AVAILABLE TO ORDER
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
alpha-Amino-beta-methylvaleric acid | erythro-L-Isoleucine | H-Ile-OH | 2-Amino-3-methylvaleric acid | (2S,3S)-2-Amino-3-methylpentanoic acid | (S)-Isoleucine | 2S,3S-Isoleucine | ISOLEUCINE, L- | L-(+)-Isoleucine | Isoleucine | L-Ile | l-isoleucine | (S,
Storage
Room temperature,Desiccated,Cool
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
25g
I103488-25g
≥10
$9.90
50g
I103488-50g
2
$11.90
100g
I103488-100g
≥10
$15.90
250g
I103488-250g
1
$31.90
500g
I103488-500g
3
$49.90
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Room temperature,Desiccated,Cool 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.

📚

Literature proof

Cited in 92 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
alpha-Amino-beta-methylvaleric acid | erythro-L-Isoleucine | H-Ile-OH | 2-Amino-3-methylvaleric acid | (2S, 3S)-2-Amino-3-methylpentanoic acid | (S)-Isoleucine | 2S, 3S-Isoleucine | ISOLEUCINE, L- | L-(+)-Isoleucine | Isoleucine | L-Ile | l-isoleucine | (S,
Specifications & Purity
Moligand™, ≥99%
Biochemical and Physiological Mechanisms
L-Isoleucine is an isomer of L-leucine and is an essential amino acid. It is synthesized from threonine and is a branched-chain hydrophobic amino acid.
Storage
Room temperature, Desiccated, Cool
Shipped In
Normal
Grade
Moligand™
Purity
≥99%
Names and Identifiers
Pubchem Sid488180047
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180047
Canonical SmilesCC[C@H](C)[C@@H](C(=O)O)N
IUPAC Name(2S,3S)-2-amino-3-methylpentanoic acid
InChIKeyAGPKZVBTJJNPAG-WHFBIAKZSA-N
INCHI1S/C6H13NO2/c1-3-4(2)5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t4-,5-/m0/s1
Isomeric SMILES CC[C@H](C)[C@@H](C(=O)O)N
RTECS NR4705000
Molecular Weight 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=

Documentation

📋 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
ClassCarboxylic 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
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
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
Associated Targets(non-human)
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
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
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 TypeDateItem
A2627474Certificate of AnalysisJan 04, 2026 I103488
A2627472Certificate of AnalysisJan 04, 2026 I103488
A2627471Certificate of AnalysisJan 04, 2026 I103488
A2627470Certificate of AnalysisJan 04, 2026 I103488
A2615403Certificate of AnalysisJan 04, 2026 I103488
A2615404Certificate of AnalysisJan 04, 2026 I103488
A2615405Certificate of AnalysisJan 04, 2026 I103488
A2615429Certificate of AnalysisJan 04, 2026 I103488
A2627467Certificate of AnalysisJan 04, 2026 I103488
L2108231Certificate of AnalysisSep 09, 2025 I103488
E2512318Certificate of AnalysisApr 28, 2025 I103488
E2512321Certificate of AnalysisApr 28, 2025 I103488
E2512324Certificate of AnalysisApr 28, 2025 I103488
E2512328Certificate of AnalysisApr 28, 2025 I103488
E2512281Certificate of AnalysisApr 28, 2025 I103488
E2512238Certificate of AnalysisApr 28, 2025 I103488
F2516265Certificate of AnalysisApr 28, 2025 I103488
F2516266Certificate of AnalysisApr 28, 2025 I103488
F2516374Certificate of AnalysisApr 28, 2025 I103488
F2516375Certificate of AnalysisApr 28, 2025 I103488
F2516376Certificate of AnalysisApr 28, 2025 I103488
F2516377Certificate of AnalysisApr 28, 2025 I103488
F2516378Certificate of AnalysisApr 28, 2025 I103488
D2521038Certificate of AnalysisSep 20, 2024 I103488
I2429259Certificate of AnalysisSep 20, 2024 I103488
I2429268Certificate of AnalysisSep 20, 2024 I103488
I2429269Certificate of AnalysisSep 20, 2024 I103488
I2429270Certificate of AnalysisSep 20, 2024 I103488
A2409334Certificate of AnalysisJan 02, 2024 I103488
A2409333Certificate of AnalysisJan 02, 2024 I103488
A2409335Certificate of AnalysisJan 02, 2024 I103488
A2409336Certificate of AnalysisJan 02, 2024 I103488
A2409337Certificate of AnalysisJan 02, 2024 I103488
I2319183Certificate of AnalysisAug 28, 2023 I103488
I2319182Certificate of AnalysisAug 28, 2023 I103488
I2319181Certificate of AnalysisAug 28, 2023 I103488
I2319180Certificate of AnalysisAug 28, 2023 I103488
F2320292Certificate of AnalysisMay 31, 2023 I103488
I2511002Certificate of AnalysisMay 31, 2023 I103488
F2320290Certificate of AnalysisMay 31, 2023 I103488
F2320298Certificate of AnalysisMay 31, 2023 I103488
F2320299Certificate of AnalysisMay 31, 2023 I103488
F2320304Certificate of AnalysisMay 31, 2023 I103488
F2320346Certificate of AnalysisMay 31, 2023 I103488
C23111072Certificate of AnalysisFeb 14, 2023 I103488
C23111091Certificate of AnalysisFeb 14, 2023 I103488
C23111080Certificate of AnalysisFeb 14, 2023 I103488
C23111079Certificate of AnalysisFeb 14, 2023 I103488
C23111066Certificate of AnalysisFeb 14, 2023 I103488
C23111064Certificate of AnalysisFeb 14, 2023 I103488
C23111065Certificate of AnalysisFeb 14, 2023 I103488
H2219292Certificate of AnalysisJul 28, 2022 I103488
H2219290Certificate of AnalysisJul 28, 2022 I103488
H2219289Certificate of AnalysisJul 28, 2022 I103488
B2328359Certificate of AnalysisJul 28, 2022 I103488
H2219288Certificate of AnalysisJul 28, 2022 I103488
H2219287Certificate of AnalysisJul 28, 2022 I103488
H2219286Certificate of AnalysisJul 28, 2022 I103488

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Chemical and Physical Properties
SolubilitySoluble in water. Slightly soluble in hot alcohol and hot acetic acid. Insoluble in ether.
Specific Rotation[α]40.5 ° (C=4, 6mol/L HCl)
Melt Point(°C)288 °C
Molecular Weight131.170 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
Documents & Articles
Citations of This Product
References
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62. En Zhang, Peng-Yan Bai, De-Yun Cui, Wen-Chao Chu, Yong-Gang Hua, Qin Liu, Hai-Yang Yin, Yong-Jie Zhang, Shangshang Qin, Hong-Min Liu.  (2017)  Synthesis and bioactivities study of new antibacterial peptide mimics: The dialkyl cationic amphiphiles.  EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,      [PMID:29126736] [10.1016/j.ejmech.2017.10.044]
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64. Zhipeng Liu, Chunying Teng, Wenting Wan, Fan Wu, Chao Wu, Weiping Ji, Yujuan Shan.  (2024)  A panel of four plasma amino acids is a promising biomarker for newly diagnosed bladder cancer.  CLINICAL NUTRITION,      [PMID:38776618] [10.1016/j.clnu.2024.05.003]
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68. Chunlei Tan, Lei Peng, Mingming Wang, Hongyu Mu, Feng Zhang, Si Huang, Kuan Wu, Jun Sheng, Yang Tian, Cunchao Zhao.  (2024)  High temperature steaming pretreatment improves quality and flavor of the walnut meal soy sauce.  LWT-FOOD SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.lwt.2024.117249]
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76. Meilin Hao, Junhong Zhu, Yuxiao Xie, Wenjie Cheng, Lanlan Yi, Sumei Zhao.  (2024)  Targeted metabolomics of muscle amino acid profles and hepatic transcriptomics analyses in grass carp (Ctenopharyngodon idellus) fed with broad beans.  Heliyon,      [PMID:39386830] [10.1016/j.heliyon.2024.e38323]
77. Lu Qin, Zhixiang Cui, Ziwei Zhang, Qiyao Zhai, Yu Wu, Jian Guan, Enyu Xu, Xin Zhang, Shirui Mao.  (2025)  Biomimetic chitosan derivatives inspired by cell-penetrating peptides for enhanced octreotide absorption following lung delivery.  CARBOHYDRATE POLYMERS,      [PMID:40973249] [10.1016/j.carbpol.2025.124251]
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89. Jie Du, Chaoqun Li, Li Chai, Fabao Zhao, Lin Lv, Zongcheng Yang, Zhiyuan Zhao, Rong Gong, Liu Yang, Meng Wu, Meng Nie, Jihui Jia, Dongwei Kang, Chengjiang Gao, Wei Zhao, Mutian Jia.  (2026)  Asparagine sensing by TBK1 controls its phase separation to drive antiviral innate immune responses.  MOLECULAR CELL,  86  (4): (722-739).  [PMID:41653919] [10.1016/j.molcel.2026.01.010]
90. Yingying Zeng, Weiwei He, Yuhao Li, Junyi Yin, Mingyong Xie.  (2026)  Effects of Phenylalanine, Valine, Isoleucine, and Leucine on the Composition and Flavor of Lactic Acid Bacteria-Fermented Celery.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2026.108557]
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