DL-NORPHENYLEPHRINE HYDROCHLORIDE

DL-NORPHENYLEPHRINE HYDROCHLORIDE Basic information
Product Name:DL-NORPHENYLEPHRINE HYDROCHLORIDE
Synonyms:alpha-(aminomethyl)-3-hydroxy-benzenemethanohydrochloride;alpha-aminomethyl-3-hydroxy-benzylalcohohydrochloride;m-octopaminehydrochloride;norfenefrin;α-(AMinoMethyl)-3-hydroxybenzeneMethanol;3-(2-aMino-1-hydroxyethyl)phenol hydrochloride;Phenylephrine Impurity A HCl (racemic Norphenylephrine HCl);Phenylephrine, Neosynephrine, Neophyrin, Mesaton
CAS:4779-94-6
MF:C8H12ClNO2
MW:189.64
EINECS:225-323-6
Product Categories:Amines;Aromatics;API;Intermediates & Fine Chemicals;Pharmaceuticals;Impuritues
Mol File:4779-94-6.mol
DL-NORPHENYLEPHRINE HYDROCHLORIDE Structure
DL-NORPHENYLEPHRINE HYDROCHLORIDE Chemical Properties
Melting point 162-164 °C(lit.)
storage temp. -20°C Freezer, Under Inert Atmosphere
solubility DMSO (Slightly), Methanol (Slightly), Water (Slightly)
form Solid
color White to Off-White
Merck 14,6699
Safety Information
Hazard Codes Xn
Risk Statements 22
WGK Germany 3
RTECS DN7400000
HS Code 2922504500
ToxicityLD50 oral in rat: 390mg/kg
MSDS Information
ProviderLanguage
SigmaAldrich English
DL-NORPHENYLEPHRINE HYDROCHLORIDE Usage And Synthesis
Chemical Propertieswhite to almost white crystalline powder
OriginatorZordel,Grelan,Japan,1970
Usesrac Norphenylephrine Hydrochloride is an Impurity A of phenylephrine. A phenylephrine derivative as leukotriene D4 antagonists.
DefinitionChEBI: Norfenefrine hydrochloride is a member of phenols.
Manufacturing Process100 parts of the hydrochloride of meta-hydroxy-ω-aminoacetophenone of melting point 220°C to 222°C (obtainable by brominating metaacetoxyacetophenone, causing the bromoketone to react with sodium iodide, adding hexamethylenetetramine to the iodide in an indifferent solvent and scission of the addition product in acid solution) are shaken in aqueous solution with hydrogen in presence of 2 parts of palladium catalyst until 2 atomic proportions of hydrogen have been absorbed. The catalyst is now filtered and the filtrate evaporated in a vacuum; and the crystalline and completely dry residue is dissolved in absolute alcohol and a precipitate is produced by adding dry ether. The hydrochloride of metahydroxyphenylethanolamine thus obtained forms white crystals of melting point 159°C to 160°C.
Therapeutic FunctionAdrenergic
DL-NORPHENYLEPHRINE HYDROCHLORIDE Preparation Products And Raw materials
Raw materialsHexamethylenetetramine-->Hydrogen-->3'-Acetoxyacetophenone-->Sodium iodide
2,2-Dichloro-1-(3-hydroxyphenyl)-ethanone N-(2-Succinyl) Phenylephrine (R)-(-)-Phenylephrine-d3 HCl 2-AMINO-3'-HYDROXY-ACETOPHENONE HYDROCHLORIDE 1,2,3,4-Tetrahydro-4,8-dihydroxy-2-methyl-isoquinoline Phenylephrine O-Aryl Sulfate N-Methyl-3,3-diphenylpropylamine ADRENOCHROME Phenylephrine D3 2R,S-HYDROXY-4[[(2R)-2-HYDROXY-2-(3-HYDROXYPHENYL)ETHYL]METHYLAMINO]-4-OXO-BUTANOIC ACID (S)-Phenylephrine hydrochloride Phenylephrine Impurity 51 (+/-)-NOREPINEPHRINE HCL L-PHENYLEPHRINE BITARTRATE (-)-Phenylephrine hydrogentartrate Norfenefrine hydrochloride ANTI-JUND DL-PHENYLEPHRINE HYDROCHLORIDE Norphenylephrine Hydrochloride

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