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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock (±)-Synephrine - Moligand™, 10mM in DMSO , CAS No.94-07-5
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. 10mM in DMSO Synonyms
Synephrine|Oxedrine|94-07-5|p-Synephrine|Parasympatol|Sympaethamine|Sympatol|Analeptin|Sympaethamin|Synephrin|Synthenate|Simpalon|(+/-)-Synephrine|Simpatol|Ethaphene|Sympathol|4-[1-Hydroxy-2-(methylamino)ethyl]phenol|DL-SYNEPHRINE|p-Oxedrine|4-(1-Hydroxy-
Shipped In
Dry ice packs + Cold packs
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Why this grade Moligand™, 10mM in DMSO Moligand™ 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.
Specifications Synonymes
Synephrine | Oxedrine | 94-07-5 | p-Synephrine | Parasympatol | Sympaethamine | Sympatol | Analeptin | Sympaethamin | Synephrin | Synthenate | Simpalon | (+/-)-Synephrine | Simpatol | Ethaphene | Sympathol | 4-[1-Hydroxy-2-(methylamino)ethyl]phenol | DL-SYNEPHRINE | p-Oxedrine | 4-(1-Hydroxy-
Spécifications et pureté
Moligand™, 10mM in DMSO
Mécanismes biochimiques et physiologiques
Selective α 1 adrenoceptor agonist. Shows vasoconstrictive and antidepressant effects in vivo. Orally active.
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.
Noms et identifiants Pubchem Sid 528775762 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/528775762 Sourires canoniques CNCC(C1=CC=C(C=C1)O)O IUPAC Name 4-[1-hydroxy-2-(methylamino)ethyl]phenol InChIKey YRCWQPVGYLYSOX-UHFFFAOYSA-N INCHI 1S/C9H13NO2/c1-10-6-9(12)7-2-4-8(11)5-3-7/h2-5,9-12H,6H2,1H3 Isomères SMILES CNCC(C1=CC=C(C=C1)O)O WGK Allemagne 3 PubChem CID 7172 Poids moléculaire 167.21
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 Benzenoids Classe Phenols Subclass 1-hydroxy-2-unsubstituted benzenoids Intermediate Tree Nodes Not available Direct Parent 1-hydroxy-2-unsubstituted benzenoids Alternative Parents Aralkylamines Benzene and substituted derivatives Secondary alcohols 1,2-aminoalcohols Dialkylamines Organopnictogen compounds Hydrocarbon derivatives Aromatic alcohols Molecular Framework Aromatic homomonocyclic compounds Substituents 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Monocyclic benzene moiety - 1,2-aminoalcohol - Secondary alcohol - Secondary amine - Secondary aliphatic amine - Organic oxygen compound - Aromatic alcohol - Alcohol - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organopnictogen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as 1-hydroxy-2-unsubstituted benzenoids. These are phenols that a unsubstituted at the 2-position. External Descriptors phenols - ethanolamines - phenethylamine alkaloid 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 Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Point de fusion (°C) 166°C-167°C Poids moléculaire 167.200 g/mol XLogP3 -0.600 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 3 Exact Mass 167.095 Da Monoisotopic Mass 167.095 Da Topological Polar Surface Area 52.500 Ų Heavy Atom Count 12 Formal Charge 0 Complexity 122.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
Citations of This Product Références 1. Yang Zhang, Shanshan Wang, Jianguang Luo, Yaolan Lin, Xiao Xu, Chao Han, Lingyi Kong. (2018) Preparative enantioseparation of synephrine by conventional and pH-zone-refining counter-current chromatography. JOURNAL OF CHROMATOGRAPHY A, [PMID:30224280 ] [10.1016/j.chroma.2018.09.012 ]
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