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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Alloxan monohydrate - 10mM in DMSO , CAS No.2244-11-3
Disponível para encomenda
GRADE & PURITY 10mM in DMSO
Synonyms
2244-11-3|Pyrimidine-2,4,5,6(1H,3H)-tetraone hydrate|Alloxan, monohydrate|2,4,5,6(1H,3H)-Pyrimidinetetrone, monohydrate|Alloxan (hydrate)|5,6-Dioxyuracil|1,3-diazinane-2,4,5,6-tetrone hydrate|2,4,5,6-Tetraoxohexahydropyrimidine hydrate|Alloxan monohydrate
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Visão geral A cytotoxic compound that causes oxidative base damage to nuclear DNA.
Specifications Sinónimos
2244-11-3 | Pyrimidine-2,4,5,6(1H,3H)-tetraone hydrate | Alloxan, monohydrate | 2,4,5,6(1H,3H)-Pyrimidinetetrone, monohydrate | Alloxan (hydrate) | 5,6-Dioxyuracil | 1,3-diazinane-2,4,5,6-tetrone hydrate | 2,4,5,6-Tetraoxohexahydropyrimidine hydrate | Alloxan monohydrate
Especificações e pureza
10mM in DMSO
Mecanismos bioquímicos e fisiológicos
Alloxan monohydrate is a hydrated form of Alloxan, which has been shown to destroy β cells. Alloxan is also used in research models to induce diabetes.Pyrimidine derivative. Glucose analog. Selectively cytotoxic to β-cells. Induces oxidative base damage t
Condições de armazenamento de armazenamento
Store at -80°C
Enviado em
Dry ice packs + Cold packs
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Nomes e identificadores Sorrisos canónicos
C1(=O)C(=O)NC(=O)NC1=O.O
IUPAC Name
1,3-diazinane-2,4,5,6-tetrone;hydrate
InChIKey
DSXMTJRUNLATRP-UHFFFAOYSA-N
INCHI
1S/C4H2N2O4.H2O/c7-1-2(8)5-4(10)6-3(1)9;/h(H2,5,6,8,9,10);1H2
SMILES isoméricas
C1(=O)C(=O)NC(=O)NC1=O.O
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5309394&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 Kingdom Organic compounds Superclass Organoheterocyclic compounds Classe Diazines Subclass Pyrimidines and pyrimidine derivatives Intermediate Tree Nodes Pyrimidones Direct Parent Barbituric acid derivatives Alternative Parents N-acyl ureas Diazinanes Dicarboximides Cyclic ketones Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aliphatic heteromonocyclic compounds Substituents Barbiturate - Ureide - N-acyl urea - 1,3-diazinane - Dicarboximide - Ketone - Cyclic ketone - Urea - Carbonic acid derivative - Carboxylic acid derivative - Azacycle - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Aliphatic heteromonocyclic compound Descrição This compound belongs to the class of organic compounds known as barbituric acid derivatives. These are compounds containing a perhydropyrimidine ring substituted at C-2, -4 and -6 by oxo groups. External Descriptors Not available 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.
Estrutura 3D Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Sensibilidade Heat & Air sensitive. Ponto de fusão (°C) 255 °C Peso molecular 160.090 g/mol XLogP3 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 0 Exact Mass 160.012 Da Monoisotopic Mass 160.012 Da Topological Polar Surface Area 93.300 Ų Heavy Atom Count 11 Formal Charge 0 Complexity 222.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 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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