L-Leucine - UltraBio™, Ultra pure, ≥99.5%(NT) , CAS No.61-90-5

CAS: 61-90-5 Cat. No.: L433129 Formule: C6H13NO2 Poids moléculaire: 131.17 Beilstein Registry Number: 4437 Numéro CE: 200-522-0
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ UltraBio™ ? UltraBio™ — Aladdin's line for molecular-biology applications. Use for nuclease-free, high-consistency reagents across molecular workflows. Ultra pure ? Ultra-pure grade with very low impurity content across the board. Use for trace analysis, electronics, or processes intolerant of contamination. ≥99.5%(NT)
Synonyms
(S)-2-Amino-4-methylpentanoic acid
Storage
Protected from light,Room temperature
Shipped In
Normal
★
Taille
Allemagne (EU)
USA*
Prix
Qté
25g
L433129-25g
—
3 En stock
84,95€
100g
L433129-100g
—
2 En stock
277,59€
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Pourquoi cette qualité

UltraBio™, Ultra pure, ≥99.5%(NT) Ultra pure,UltraBio™ pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Protected from light,Room temperature Expédition Normal. Consultez le COA spécifique au lot pour les spécifications exactes.

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Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 359 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

Other Notes

As spacer in isotachophoresis of serum proteins; Growth requirement of various microorganisms

Spécifications

Synonymes
(S)-2-Amino-4-methylpentanoic acid
Spécifications et pureté
UltraBio™, Ultra pure, ≥99.5%(NT)
Conditions de stockage de stockage
Protected from light,Room temperature
Expédié en
Normal
Grade
Ultra pure, UltraBio™
Pureté
≥99.5%(NT)
Noms et identifiants
Pubchem Sid
Sourires canoniques
CC(C)CC(C(=O)O)N
IUPAC Name
(2S)-2-amino-4-methylpentanoic acid
InChIKey
ROHFNLRQFUQHCH-YFKPBYRVSA-N
INCHI
1S/C6H13NO2/c1-4(2)3-5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t5-/m0/s1
Isomères SMILES
CC(C)C[C@@H](C(=O)O)N
WGK Allemagne
1
Poids moléculaire
131.17
Beilstein
4437
Reaxy-Rn
636005
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=636005&ln=

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

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📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

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🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

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Données avancées

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 ParentLeucine 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 Leucine 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 leucine and derivatives. These are compounds containing leucine or a derivative thereof resulting from reaction of leucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Common amino acids
Structure 3D
Modèle de structure chimique interactif





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Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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3 results found

Lot NumberCertificate TypeDateArticle
I2609118I2609118Certificate of AnalysisOct 28, 2024 L433129
J2423106J2423106Certificate of AnalysisOct 28, 2024 L433129
J2423107J2423107Certificate of AnalysisOct 28, 2024 L433129
Propriétés chimiques et physiques
Solubilité1 M HCl: 0.1M at20°C, clear, colorless
SensibilitéMoisture and light sensitive.
Rotation spécifique [α][α]20/D +15.5±0.5°, c = 5% in 5 M HCl
Point d'ébullition (°C)122-134 °C
Point de fusion (°C)270-340 °C (decomposition)
Poids moléculaire131.170 g/mol
XLogP3-1.500
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
Complexity101.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQ et articles
UltraBio™: Defining Excellence in Molecular Biology Applications
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
Central–Peripheral Signaling Networks Regulated by Neuropeptides and the Integration of Energy Metabolism
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
Catalytic Mechanisms of the Aminotransferase Family and Regulation of Amino Acid Metabolism
Citations of This Product
Calculateurs de solution
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