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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Tazobactam Sodium Salt - ≥98% , Bacterial beta-lactamase TEM inhibitor, CAS No.89785-84-2, Bacterial beta-lactamase TEM inhibitor
Synonyms
Triethylamine, ZerO2(TM), >=99% | D03707 | sodium (2S,3S,5R)-3-methyl-4,4,7-trioxo-3-[(1H-1,2,3-triazol-1-yl)methyl]-4lambda(6)-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate | Tazobactam sodium salt | RFMIKMMOLPNEDG-QVUDESDKSA-M | 4-Thia-1-azabicyclo(3.2.
Storage
Store at 2-8°C,Protected from light,Argon charged
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Protected from light,Argon charged Ships Wet ice 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Descripción general Tazobactam sodium is a LACTB (β-lactamase) inhibitor and antibacterial.
Specifications Sinónimos
Triethylamine, ZerO2(TM), >=99% | D03707 | sodium (2S, 3S, 5R)-3-methyl-4, 4, 7-trioxo-3-[(1H-1, 2, 3-triazol-1-yl)methyl]-4lambda(6)-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate | Tazobactam sodium salt | RFMIKMMOLPNEDG-QVUDESDKSA-M | 4-Thia-1-azabicyclo(3.2.
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Tazobactam is a β -Lactamase inhibitor. When used with β-lactam antibiotics I, it enhances their effect.
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Protected from light, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Mecanismo de acción
Bacterial beta-lactamase TEM inhibitor
Nombres e identificadores Sonrisas canónicas CC1(C(N2C(S1(=O)=O)CC2=O)C(=O)[O-])CN3C=CN=N3.[Na+] IUPAC Name sodium;(2S,3S,5R)-3-methyl-4,4,7-trioxo-3-(triazol-1-ylmethyl)-4λ6-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate InChIKey RFMIKMMOLPNEDG-QVUDESDKSA-M INCHI 1S/C10H12N4O5S.Na/c1-10(5-13-3-2-11-12-13)8(9(16)17)14-6(15)4-7(14)20(10,18)19;/h2-3,7-8H,4-5H2,1H3,(H,16,17);/q;+1/p-1/t7-,8+,10+;/m1./s1 Isómeros SMILES C[C@@]1([C@@H](N2[C@H](S1(=O)=O)CC2=O)C(=O)[O-])CN3C=CN=N3.[Na+] PubChem CID 23663400 Peso molecular 322.27
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 Kingdom Organic compounds Superclass Organic acids and derivatives Clase Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives Direct Parent Alpha amino acids and derivatives Alternative Parents Penams Triazoles Thiazolidines Tertiary carboxylic acid amides Sulfones Heteroaromatic compounds Azetidines Carboxylic acid salts Azacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Hydrocarbon derivatives Organic zwitterions Organopnictogen compounds Organonitrogen compounds Carbonyl compounds Organic oxides Organic sodium salts Molecular Framework Aromatic heteropolycyclic compounds Substituents Alpha-amino acid or derivatives - Penam - Azole - Beta-lactam - Sulfone - Heteroaromatic compound - Tertiary carboxylic acid amide - Thiazolidine - 1,2,3-triazole - Azetidine - Carboxamide group - Carboxylic acid salt - Lactam - Organic alkali metal salt - Azacycle - Organoheterocyclic compound - Carboxylic acid - Monocarboxylic acid or derivatives - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic oxide - Organic nitrogen compound - Carbonyl group - Organopnictogen compound - Organic sodium salt - Organic zwitterion - Organic salt - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. External Descriptors organic sodium salt Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Soluble in water (100 mg/ml), and methanol. Sensibilidad Air sensitive；Moisture sensitive；Heat sensitive Índice de refracción 1.82 Punto de ebullición (°C) 707.1° C Punto de fusión (°C) 140-147°C Peso molecular 322.280 g/mol XLogP3 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 3 Exact Mass 322.035 Da Monoisotopic Mass 322.035 Da Topological Polar Surface Area 134.000 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 578.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 3 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 2
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