L-allo-Isoleucine - ≥98% , CAS No.1509-34-8

CAS: 1509-34-8 Cat. No.: I113733 Peso molecular: 131.17 Beilstein Registry Number: 1721791 Número EC: 216-142-3
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
G22N65IL3O | Tox21_112304 | (+/-)-ALLO-ISOLEUCINE | [S-(R*,S*)]-2-Amino-3-methylpentanoic acid | CHEBI:43433 | Pentanoic acid, 2-amino-3-methyl-, (S-(R*,S*))- | Verzenios | A809090 | DB01739 | 4-[4-[4-(4-hydroxyphenyl)piperazin-1-yl]phenyl]-2-[(2S,3S)-2-p
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
100mg
I113733-100mg
3
76,90US$
200mg
I113733-200mg
2
121,90US$
500mg
I113733-500mg
2
160,90US$
1g
I113733-1g
2
304,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

L-Alloisoleucine is a branched chain amino acid and is a stereo-isomer of L-isoleucine. L-Alloisoleucine is a common constituent of human plasma.

Specifications

Sinónimos
G22N65IL3O | Tox21_112304 | (+/-)-ALLO-ISOLEUCINE | [S-(R*, S*)]-2-Amino-3-methylpentanoic acid | CHEBI:43433 | Pentanoic acid, 2-amino-3-methyl-, (S-(R*, S*))- | Verzenios | A809090 | DB01739 | 4-[4-[4-(4-hydroxyphenyl)piperazin-1-yl]phenyl]-2-[(2S, 3S)-2-p
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Isoleucine can be used in the study of maple diabetes.
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504756431
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504756431
Sonrisas canónicasCCC(C)C(C(=O)O)N
IUPAC Name(2S,3R)-2-amino-3-methylpentanoic acid
InChIKeyAGPKZVBTJJNPAG-UHNVWZDZSA-N
INCHI1S/C6H13NO2/c1-3-4(2)5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t4-,5+/m1/s1
Isómeros SMILES CC[C@@H](C)[C@@H](C(=O)O)N
WGK Alemania 3
Peso molecular 131.17
Beilstein 1721791
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
ClaseCarboxylic 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
DescripciónThis 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 non-proteinogenic L-alpha-amino acid - alloisoleucine
Estructura 3D
Modelo de Estructura Química Interactiva





Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

10 results found

Lot NumberCertificate TypeFechaArticulo
A2628191Certificate of AnalysisMar 22, 2025 I113733
H2504499Certificate of AnalysisMar 22, 2025 I113733
H2504530Certificate of AnalysisMar 22, 2025 I113733
H2512593Certificate of AnalysisMar 22, 2025 I113733
B2320290Certificate of AnalysisJan 06, 2023 I113733
B2320294Certificate of AnalysisJan 06, 2023 I113733
B2320296Certificate of AnalysisJan 06, 2023 I113733
L1821028Certificate of AnalysisOct 18, 2022 I113733
L1821027Certificate of AnalysisOct 18, 2022 I113733
B2217088Certificate of AnalysisFeb 19, 2022 I113733
Propiedades químicas y físicas
Rotación específica [α]37° (C=4,6mol/L HCl)
Punto de fusión (°C)272 °C(dec.)
Peso molecular131.170 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
Citations of This Product
Referencias
1. Bochuan Yuan, Ziwei Wu, Wei Ji, Dong Liu, Xiang Guo, Donghui Yang, Aili Fan, Hongli Jia, Ming Ma, Wenhan Lin.  (2021)  Discovery of cyclohexadepsipeptides with anti-Zika virus activities and biosynthesis of the nonproteinogenic building block (3S)-methyl-l-proline.  JOURNAL OF BIOLOGICAL CHEMISTRY,  297  (1):   [PMID:34029593] [10.1016/j.jbc.2021.100822]
Calculadoras de soluciones
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