Propanol Hydrochloride

Chemical Neme 1 -[4-[2-(Cyclopropylmethoxy)ethyl]phenoxy ]-3-[(1 -methylethyl)amino] 2-propanol hydrochloride... 

Common Name 3-(4-carboethoxy-4-phenylpiperidino)-1-phenyl-1-propanol hydrochloride Structural Formula ... 

Common Name dl-norephedrine hydrochloride 2-amino-1-phenyl-1-propanol hydrochloride... 

The base may be converted into the hydrochloride as follows. 4.65 parts of the base are dissolved in 60 parts of warm acetone. To the warm solution there are added 2 parts of 10 N hydrochloric acid. The mixture is allowed to cool, and is then filtered. The solid residue is washed with acetone and then dried. The solid is crystallized from propanol, and there is thus obtained 1-isopropylamino-3-(1-naphthoxy)-2-propanol hydrochloride MP 163°C. 

H5C6-CO-CH-CHj NHj Cle erythro-2-Amino-1 -phenyl-propanol-Hydrochlorid Na[BH4] 85 191 4... 

Halloysite was found to be a viable and inexpensive nanoscale container for the encapsulation of biologically active molecules and drugs as was first demonstrated by Price et al. [5-8]. Its physicochemical characterization as a novel drug delivery system was also reported by Levis and Deasy et al. [9,10], who further demonstrated the controlled release of diltiazem hydrochloride and propanol hydrochloride... 

Chemical Name l-[(l-Methylethyl)amino]-3-[2-(2-propenyl)phenoxy]-2-propanol hydrochloride... 

Common Name 3-(4-Carboethoxy-4-phenylpiperidino)-l-phenyl-l-propanol hydrochloride... 

Therapeutic Function Antiparkinsonian, Anticholinergic Chemical Name l,l-Diphenyl-3-piperidino-l-propanol hydrochloride Common Name Pridinol Ridinol Structural Formula ... 

A suspension of 1-p-benzyloxyphenoxy-2,3-epoxypropane (11.5 g) in isopropanol (6 ml) is added to a stirred mixture of 4-(N-beta-aminoethylcarbamoyl) morpholine hydrogen sulphate (12.7 g), potassium hydroxide (7.0 g) and isopropanol (10 ml) and the mixture is stirred at 45°C for 1 hour and then evaporated to dryness under reduced pressure. The residual oil is stirred with water, the mixture is filtered and the solid residue is dissolved in acetone. A 30% solution of hydrogen chloride in propanol is added until the pH of the mixture is less than 2, and the mixture is filtered. The solid residue is crystallised from water and there is thus obtained 1-p-benzyloxyphenoxy-3-(beta-morpholinocarbonamidoethyl)amino-2-propanol hydrochloride (4.9 g). 

York P, et al. 1998. Characterisation of the surface energetics of milled dl-propanol hydrochloride using inverse gas chromatography and molecular modeling. Int. J. Pharm. 174 ... 

SYN S 2-AMINO-l -(2,5-DIMETHOXYPHENYL)-l -PROPANOL HYDROCHLORIDE a-(l-AMINOETHYL)-2,5-DIMETHOXYBENZYL ALCOHOL HYDROCHLORIDE p-(2,5-DIMETHOX1THENYL)-p-HYDROXYISO-PROPYL.AMINE HYDROCHLORIDE p-HYDROXY-P-(2,5-DIMETHOXYPHENYL)-ISOPROPYLAi nNE HYDROCHLORIDE PRESSOMIN HYDROCHLORIDE VASO-XINE VASOXINE HYDROCHLORIDE VASOXYL HYDROCHLORIDE... 

SYNS a-(l-AMINOETHYL)BENZENEMETHANOL HYDROCHLORIDE a-(l-AMINOETHYL)BENZYL ALCOHOL HYDROCHLORIDE ( )-2-AMINO-l-PHENYL-l-PROPANOL HYDROCHLORIDE O-HYDROXY-P-AMINOPROPYLBENZENE HYDROCHLORIDE MONHYDRIN MUCORAMA MYDRIATINE dl-NOREPHEDRINE HYDROCHLORIDE dl-l-PHENYL-2-AMINO-l-PROPANOL MONOHYDROCHLORIDE PHENYLPROPANOLAMINE HYDROCHLORIDE... 

AMINO-l-PHENYL-l-PROPANOL see NNMOOO ( )-2-AMINO-l -PHENYL-1 -PROPANOL HYDROCHLORIDE see PMJ500... 

C9H120 2-methyl-6-ethylphenol 1687-64-5 21.88 0.9809 2 17334 C9H13N02 3-amino-1 -phenoxy-2-propanol hydrochloride 4287-20-1 25.00 1.0984 2... 

Racemic compounds, or true racemates, exhibit two eutectic points each between the pure enantiomer and the racemic compound. The shape of the DSC diagrams can vary, depending on the relative positions of temperatures of eutectics and racemic compound and on the composition of the eutectics (Figs. 16B and C). In the case of Fig. 16C it is difficult to distinguish by DSC a racemic compound from a conglomerate. Other methods as IR or X-ray are suitable for proper interpretation. For example, propanol hydrochloride has been described as conglomerate or as racemate compound. ... 

The formation of cyclopropanols by C-O bond cleavage has been achieved under a variety of conditions (Table 1). In most cases the syntheses were carried out under acidic conditions, in the presenee of sulfuric acid, hydrochloric acid, pyridinium p-toluenesulfonate, boron tribromide, or an aqueous acid, to cleave esters, ethers, ° and acetals. Other acid-sensitive moieties in the substrate can react concomitantly under such conditions. Thus, when rer/-butyl-(l-ethoxycyclopropyl)carbamate was heated in hydrochloric acid at 60 "C both the ether and the carbamate functions reacted to give 1-aminocyclo-propanol hydrochloride. 1-Acetoxycyclopropanecarbonitrile, on the other hand, was converted to 1-hydroxycyclopropanecarbonitrile under similar conditions. ... 

Methoxamine Hydrochloride, a-(t-Aminoethyt)-2,5-dimethoxybenzenemethanol hydrochloride a-(l-amino-ethy )-2,5-dimethoxybenzyl alcohol hydrochloride 2-amino-I -(2,5-dimethoxyphenyl)-1 -propanol hydrochloride o -h -droxy-.7-C2.5-dimethoxyphenyl)isopropy[amine hydrochloride -(2,5-dimethoxyphenyl)-6-hydroxyisopropylamine hydrochloride 2,5 -dimethoxynorephedrine hydrochloride Pressomm Hydrochloride Vasoxine Hydrochloride Vasoxyl Hydrochloride Vasylox Hydrochloride. <.H ,C1 NOy. mol wt 247.71. C 53.33%, H 7.32%, N 5,66%, Cl 14.31%, O... 

Chemical Name 1-(isopropylamino)-3-(1-naphthyloxy)-2-propanol hydrochloride Common Name —... 

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