(1S,2S)-(+)-Pseudoephedrine Hydrochloride CAS#345-78-8
(1S,2S)-(+)-Pseudoephedrine hydrochloride takes the form of a white crystalline powder, characterized by a bitter taste and the absence of any obvious odour. This compound dissolves freely in water, shows limited solubility in ethanol, and remains insoluble in chloroform and diethyl ether. As a vital pharmaceutical raw material, it is extensively employed for the production of compound cold preparations and many other medicinal goods. Furthermore, it acts as a precious intermediate for organic synthesis and supports the fabrication of a broad selection of organic molecules.
(1S,2S)-(+)-Pseudoephedrine hydrochloride Chemical Properties
Product Name: | (1S,2S)-(+)-Pseudoephedrine hydrochloride |
Synonyms: | (+)-PSI-EPHEDRINE HYDROCHLORIDE;PSI-EPHEDRINE HYDROCHLORIDE;PSEUDOEPHEDRINE HCL;PSEUDOEPHEDRINE HCL, (+)-1S,2S-;PSEUDOEPHEDRINE HYDROCHLORIDE;a)]-;alpha-(1-(methylamino)ethyl)-,hydrochloride,(s-(r*,r*))-benzenemethano;benzenemethanol,alpha-[1-(methylamino)ethyl]-,hydrochloride,[s-(theta,thet |
CAS: | 345-78-8 |
MF: | C10H16ClNO |
MW: | 201.69 |
EINECS: | 206-462-1 |
Product Categories: | Pharmaceutical Raw Materials;Amines;Aromatics;Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals;API's |
Mol File: | 345-78-8.mol |
Melting point | 185-188 °C(lit.) |
alpha | 61 º (c=5, H2O,2dm tube) |
storage temp. | Refrigerator (+4°C) |
solubility | Freely soluble in water and in ethanol (96 per cent), sparingly soluble in methylene chloride. |
pka | 9.22(at 25℃) |
form | buffered aqueous solution |
biological source | rabbit |
Merck | 138007 |
BRN | 3915112 |
LogP | -1.74 at 23℃ and pH7 |
CAS DataBase Reference | 345-78-8(CAS DataBase Reference) |
EPA Substance Registry System | Benzenemethanol, .alpha.-[(1S)-1-(methylamino)ethyl]-, hydrochloride, (.alpha.S)- (345-78-8) |
Product Usage of (1S,2S)-(+)-Pseudoephedrine Hydrochloride
Acting as a crucial intermediate for organic synthesis, (1S,2S)-(+)-Pseudoephedrine hydrochloride bears reactive functional groups that enable its participation in numerous chemical transformations. It is frequently applied to synthesize organic molecules with targeted structures and performance features, covering fine chemicals and pharmaceutical intermediates. Thanks to its broad reaction adaptability, this compound carries substantial value within organic synthesis research and production.
