Sarcosine - UltraBio™, Ultra pure , CAS No.107-97-1

CAS: 107-97-1 Cat. No.: S431365 Formule: C3H7NO2 Poids moléculaire: 89.09 Beilstein Registry Number: 4345 Numéro CE: 203-538-6 PubChem CID: 1088
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.
Synonyms
GTPL4713 | N-Cocoyl sarcosine | (Methylamino)ethanoic acid | Me-Gly-OH | (methylamino)acetate | (methylamino)-Acetate | N-Cocoyl-N-methylglycine | sarcosinate | 2-Methylaminoethanoic acid | DTXSID1047025 | CH3NHCH2COOH | BBL009707 | MeGly | AC7804 | CH3NH
Storage
Room temperature,Desiccated
Shipped In
Normal
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Taille
USA
Allemagne (EU)*
Prix
Qté
1g
S431365-1g
Sur commande · 8–12 semaines
19,90$US
5g
S431365-5g
Sur commande · 8–12 semaines
56,90$US
25g
S431365-25g
3 En stock
—
169,90$US
100g
S431365-100g
2 En stock
1 En stock
399,90$US
Enter a quantity for the sizes you want to add.
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Pourquoi cette qualité

UltraBio™, Ultra pure 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

Room temperature,Desiccated 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 56 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Spécifications

Synonymes
GTPL4713 | N-Cocoyl sarcosine | (Methylamino)ethanoic acid | Me-Gly-OH | (methylamino)acetate | (methylamino)-Acetate | N-Cocoyl-N-methylglycine | sarcosinate | 2-Methylaminoethanoic acid | DTXSID1047025 | CH3NHCH2COOH | BBL009707 | MeGly | AC7804 | CH3NH
Spécifications et pureté
UltraBio™, Ultra pure
Conditions de stockage de stockage
Room temperature,Desiccated
Expédié en
Normal
Grade
Ultra pure, UltraBio™
Noms et identifiants
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/528774929
Sourires canoniques
CNCC(=O)O
IUPAC Name
2-(methylamino)acetic acid
InChIKey
FSYKKLYZXJSNPZ-UHFFFAOYSA-N
INCHI
1S/C3H7NO2/c1-4-2-3(5)6/h4H,2H2,1H3,(H,5,6)
Isomères SMILES
CNCC(=O)O
WGK Allemagne
1
RTECS
VQ2897000
PubChem CID
1088
Poids moléculaire
89.09
Beilstein
4345
Reaxy-Rn
1699442

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)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

Rechercher le COA →

📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

Voir la fiche technique →

🔬 Fiche de spécifications

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

Voir la fiche de spécifications →

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 ParentAlpha amino acids
Alternative Parents Amino acids  Monocarboxylic acids and derivatives  Dialkylamines  Carboxylic acids  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Alpha-amino acid - Amino acid - Carboxylic acid - Secondary aliphatic amine - Monocarboxylic acid or derivatives - Secondary amine - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Amine - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).
External Descriptors N-alkylglycine - N-methyl-amino acid - N-methylglycines
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:

Find and download the COA for your product by matching the lot number on the packaging.

11 results found

Lot NumberCertificate TypeDateArticle
F2602373F2602373Certificate of AnalysisMay 22, 2026 S431365
F2602389F2602389Certificate of AnalysisMay 22, 2026 S431365
F2602391F2602391Certificate of AnalysisMay 22, 2026 S431365
F2602392F2602392Certificate of AnalysisMay 22, 2026 S431365
C2611466C2611466Certificate of AnalysisFeb 26, 2026 S431365
C2611480C2611480Certificate of AnalysisFeb 26, 2026 S431365
C2611481C2611481Certificate of AnalysisFeb 26, 2026 S431365
C2611483C2611483Certificate of AnalysisFeb 26, 2026 S431365
C2611485C2611485Certificate of AnalysisFeb 26, 2026 S431365
K2401190K2401190Certificate of AnalysisNov 14, 2024 S431365
K2401191K2401191Certificate of AnalysisNov 14, 2024 S431365
Propriétés chimiques et physiques
SolubilitéH2O: 1M, clear, colorless
SensibilitéMoisture sensitive
Point de fusion (°C)208-212°C
Poids moléculaire89.090 g/mol
XLogP3-2.800
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass89.0477 Da
Monoisotopic Mass89.0477 Da
Topological Polar Surface Area49.300 Ų
Heavy Atom Count6
Formal Charge0
Complexity52.800
Isotope Atom Count0
Defined Atom Stereocenter Count0
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
What Do Unnatural Amino Acids Really Change? Site-Specific Observation, Functional Engineering, and Property Optimization in Proteins and Peptides
Creatinine Content Detection: Main Methods, Reaction Principles, and Result Control
Analysis of Amino Acid-Based Surfactants: Basic Structure, Performance Origins, Category Selection, and Applications in Personal Care Formulations
Catalytic Mechanisms of Creatinine Metabolism-Related Enzymes and Their Applications in Renal Function Testing
Polarity Exposure and Passive Membrane Permeability of bRo5 Molecules: TPSA, EPSA, ETR, and Molecular Chameleonicity
Citations of This Product
Calculateurs de solution
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