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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Guanethidine Monosulfate - 10mM in Water , Norepinephrine transporter substrate, CAS No.645-43-2, Norepinephrine transporter substrate
GRADE & PURITY 10mM in Water
Synonyms
guanethidine sulfate|Guanethidine monosulfate|645-43-2|Ismelin|Ismelin sulfate|Guanethidine (sulfate)|Guanethidine Sulphae|guanethidine monosulphate|EINECS 211-442-0|UNII-5UBY8Y002G|Iporal|5UBY8Y002G|1-(2-(azocan-1-yl)ethyl)guanidine sulfate|N-(2-Guanidin
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.
Descripción general Guanethidine monosulfate is an antihypertensive agent that acts by inhibiting selectively transmission in post-ganglionic adrenergic nerves.
Specifications Sinónimos
guanethidine sulfate | Guanethidine monosulfate | 645-43-2 | Ismelin | Ismelin sulfate | Guanethidine (sulfate) | Guanethidine Sulphae | guanethidine monosulphate | EINECS 211-442-0 | UNII-5UBY8Y002G | Iporal | 5UBY8Y002G | 1-(2-(azocan-1-yl)ethyl)guanidine sulfate | N-(2-Guanidin
Especificaciones y pureza
10mM in Water
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Mecanismo de acción
Norepinephrine transporter substrate
Nombres e identificadores Sonrisas canónicas C1CCCN(CCC1)CCN=C(N)N.OS(=O)(=O)O IUPAC Name 2-[2-(azocan-1-yl)ethyl]guanidine;sulfuric acid InChIKey YUFWAVFNITUSHI-UHFFFAOYSA-N INCHI 1S/C10H22N4.H2O4S/c11-10(12)13-6-9-14-7-4-2-1-3-5-8-14;1-5(2,3)4/h1-9H2,(H4,11,12,13);(H2,1,2,3,4) Isómeros SMILES C1CCCN(CCC1)CCN=C(N)N.OS(=O)(=O)O Peso molecular 296.39 Reaxy-Rn 18292174 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=18292174&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 Organic acids and derivatives Clase Organic sulfuric acids and derivatives Subclass Organic sulfuric acids Intermediate Tree Nodes Not available Direct Parent Organic sulfuric acids Alternative Parents Trialkylamines Guanidines Propargyl-type 1,3-dipolar organic compounds Carboximidamides Azacyclic compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aliphatic heteromonocyclic compounds Substituents Sulfuric acid - Guanidine - Tertiary amine - Tertiary aliphatic amine - Carboximidamide - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Aliphatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as organic sulfuric acids. These are organic compounds containing the sulfuric acid functional group, with the generic structure HOS(=O)(=O)OH. External Descriptors organic sulfate 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 Sensibilidad Hygroscopic Punto de fusión (°C) 227℃ Peso molecular 296.390 g/mol XLogP3 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 3 Exact Mass 296.152 Da Monoisotopic Mass 296.152 Da Topological Polar Surface Area 151.000 Ų Heavy Atom Count 19 Formal Charge 0 Complexity 248.000 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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