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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock Oxtriphylline - 10mM in DMSO , Adenosine receptor antagonist, CAS No.4499-40-5, Adenosine receptor antagonist
GRADE & PURITY 10mM in DMSO
Synonyms
(2-Hydroxyethyl)trimethylammonium compound with theophylline | Choline thieophyllinate | OXTRIPHYLLINE [VANDF] | Sabidal | ETHANAMINIUM, 2-HYDROXY-N,N,N-TRIMETHYL-, SALT WITH 3,9-DIHYDRO-1,3-DIMETHYL-1H-PURINE-2,6-DIONE (1:1) | CHOLINE THEOPHYLLINATE [MAR
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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonymes
(2-Hydroxyethyl)trimethylammonium compound with theophylline | Choline thieophyllinate | OXTRIPHYLLINE [VANDF] | Sabidal | ETHANAMINIUM, 2-HYDROXY-N,N,N-TRIMETHYL-, SALT WITH 3,9-DIHYDRO-1,3-DIMETHYL-1H-PURINE-2,6-DIONE (1:1) | CHOLINE THEOPHYLLINATE [MAR
Spécifications et pureté
10mM in DMSO
Conditions de stockage de stockage
Store at -80°C
Expédié en
Dry ice packs + Cold packs
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Mécanisme d'action
Adenosine receptor antagonist
Noms et identifiants Pubchem Sid 528766516 Sourires canoniques CN1C(=C2C(=NC=N2)N(C1=O)C)[O-].C[N+](C)(C)CCO IUPAC Name 1,3-dimethyl-2-oxopurin-6-olate;2-hydroxyethyl(trimethyl)azanium InChIKey SOELXOBIIIBLRJ-UHFFFAOYSA-M INCHI 1S/C7H8N4O2.C5H14NO/c1-10-5-4(8-3-9-5)6(12)11(2)7(10)13;1-6(2,3)4-5-7/h3,12H,1-2H3;7H,4-5H2,1-3H3/q;+1/p-1 Isomères SMILES CN1C(=C2C(=NC=N2)N(C1=O)C)[O-].C[N+](C)(C)CCO Poids moléculaire 283.33 Reaxy-Rn 4928440 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4928440&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 Imidazopyrimidines Subclass Purines and purine derivatives Intermediate Tree Nodes Not available Direct Parent Xanthines Alternative Parents Purinones Alkaloids and derivatives Cholines Pyrimidones Tetraalkylammonium salts Heteroaromatic compounds Imidazoles Ureas 1,2-aminoalcohols Azacyclic compounds Organic salts Organic oxides Hydrocarbon derivatives Organic zwitterions Organopnictogen compounds Primary alcohols Molecular Framework Not available Substituents Xanthine - Purinone - Alkaloid or derivatives - Choline - Pyrimidone - Pyrimidine - Azole - Imidazole - Quaternary ammonium salt - Tetraalkylammonium salt - Heteroaromatic compound - Urea - 1,2-aminoalcohol - Azacycle - Alkanolamine - Amine - Organopnictogen compound - Organic oxygen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Alcohol - Organic nitrogen compound - Organic oxide - Organic zwitterion - Organic salt - Hydrocarbon derivative - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as xanthines. These are purine derivatives with a ketone group conjugated at carbons 2 and 6 of the purine moiety. 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.
Structure 3D Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Poids moléculaire 283.330 g/mol XLogP3 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 2 Exact Mass 283.164 Da Monoisotopic Mass 283.164 Da Topological Polar Surface Area 91.600 Ų Heavy Atom Count 20 Formal Charge 0 Complexity 415.000 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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