DL-NORPHENYLEPHRINE HYDROCHLORIDE
- Product Name
- DL-NORPHENYLEPHRINE HYDROCHLORIDE
- CAS No.
- 4779-94-6
- Chemical Name
- DL-NORPHENYLEPHRINE HYDROCHLORIDE
- Synonyms
- WV 569;Coritat;Vingsal;Energona;Esbuphon;Stagural;Tonolift;Molycor R;NSC 100733;NSC 297582
- CBNumber
- CB9429008
- Molecular Formula
- C8H11NO2.ClH
- Formula Weight
- 189.64
- MOL File
- 4779-94-6.mol
DL-NORPHENYLEPHRINE HYDROCHLORIDE Property
- 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
N-Bromosuccinimide Price
- Product number
- 1473206
- Product name
- Norphenylephrine hydrochloride
- Purity
- United States Pharmacopeia (USP) Reference Standard
- Packaging
- 25mg
- Price
- $1490
- Updated
- 2024/03/01
- Product number
- 113727
- Product name
- Norphenylephrine hydrochloride
- Purity
- 98%
- Packaging
- 10g
- Price
- $135
- Updated
- 2024/03/01
- Product number
- PHR1536
- Product name
- Norphenylephrine Hydrochloride
- Purity
- Pharmaceutical Secondary Standard; Certified Reference Material
- Packaging
- 200mg
- Price
- $315
- Updated
- 2024/03/01
- Product number
- N825500
- Product name
- racNorphenylephrineHydrochloride(PhenylephrineImpurityA)
- Packaging
- 250mg
- Price
- $425
- Updated
- 2021/12/16
- Product number
- IN27563
- Product name
- rac-Norphenylephrine hydrochloride
- Packaging
- 100g
- Price
- $500
- Updated
- 2021/12/16
DL-NORPHENYLEPHRINE HYDROCHLORIDE Chemical Properties,Usage,Production
Chemical Properties
white to almost white crystalline powder
Originator
Zordel,Grelan,Japan,1970
Uses
rac Norphenylephrine Hydrochloride is an Impurity A of phenylephrine. A phenylephrine derivative as leukotriene D4 antagonists.
Definition
ChEBI: Norfenefrine hydrochloride is a member of phenols.
Manufacturing Process
100 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 Function
Adrenergic
DL-NORPHENYLEPHRINE HYDROCHLORIDE Preparation Products And Raw materials
Raw materials
Preparation Products
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