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· · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino Histamine diphosphate monohydrate - 10mM in Water , Histamine H1 receptor agonist, CAS No.51-74-1, Histamine H1 receptor agonist
GRADE & PURITY 10mM in Water
Synonyms
Histamine phosphate [USP] | MFCD00064316 | Histamine Phosphate,(S) | Histamine acid phosphate | AC-24100 | DTXSID7058759 | HY-A0129 | Histamine diphosphate, 98% | Histaminephosphate | QWB37T4WZZ | Histamine phosphate (USP) | UNII-QWB37T4WZZ | 1H-Imidazole
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in Water 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.
Panoramica Histamine bisphosphate monohydrate is a potent agonist of histamine receptors.
Specifications Sinonimi
Histamine phosphate [USP] | MFCD00064316 | Histamine Phosphate,(S) | Histamine acid phosphate | AC-24100 | DTXSID7058759 | HY-A0129 | Histamine diphosphate, 98% | Histaminephosphate | QWB37T4WZZ | Histamine phosphate (USP) | UNII-QWB37T4WZZ | 1H-Imidazole
Specifiche e purezza
10mM in Water
Meccanismi biochimici e fisiologici
Phosphate salt of Histamine . Acts as a neurotransmitter in the nervous system and as a local mediator in the gut, skin, and immune system.
Condizioni di conservazione di stoccaggio
Store at -80°C
Spedito in
Dry ice packs + Cold packs
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Meccanismo d'azione
Histamine H1 receptor agonist
Nomi e identificatori Pubchem Sid 528769742 Sorrisi canonici C1=C(NC=N1)CCN.OP(=O)(O)O.OP(=O)(O)O IUPAC Name 2-(1H-imidazol-5-yl)ethanamine;phosphoric acid InChIKey ZHIBQGJKHVBLJJ-UHFFFAOYSA-N INCHI 1S/C5H9N3.2H3O4P/c6-2-1-5-3-7-4-8-5;2*1-5(2,3)4/h3-4H,1-2,6H2,(H,7,8);2*(H3,1,2,3,4) Isomeri SMILES C1=C(NC=N1)CCN.OP(=O)(O)O.OP(=O)(O)O WGK Germania 3 RTECS NI5425000 CAS alternativo 23297-93-0 Peso molecolare 325.15 Beilstein 3744619 Reaxy-Rn 6250304 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6250304&ln=
Documentazione 📋 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 nitrogen compounds Classe Organonitrogen compounds Subclass Amines Intermediate Tree Nodes Primary amines Direct Parent 2-arylethylamines Alternative Parents Aralkylamines Organic phosphoric acids and derivatives Imidazoles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents 2-arylethylamine - Aralkylamine - Organic phosphoric acid derivative - Heteroaromatic compound - Imidazole - Azole - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary aliphatic amine - Aromatic heteromonocyclic compound Descrizione This compound belongs to the class of organic compounds known as 2-arylethylamines. These are primary amines that have the general formula RCCNH2, where R is an organic group. External Descriptors phosphate 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.
Struttura 3D Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Sensibilità Heat & Moisture sensitive Punto di fusione (°C) 126-132°C Peso molecolare 307.140 g/mol XLogP3 Hydrogen Bond Donor Count 8 Hydrogen Bond Acceptor Count 10 Rotatable Bond Count 2 Exact Mass 307.033 Da Monoisotopic Mass 307.033 Da Topological Polar Surface Area 210.000 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 114.000 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 3
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