ChemicalBook > CAS DataBase List > 1-(3,4-dihydroxyphenyl)-2-[(1-methylethyl)amino] hydrochloride
1-(3,4-dihydroxyphenyl)-2-[(1-methylethyl)amino] hydrochloride
- Product Name
- 1-(3,4-dihydroxyphenyl)-2-[(1-methylethyl)amino] hydrochloride
- CAS No.
- 16899-81-3
- Chemical Name
- 1-(3,4-dihydroxyphenyl)-2-[(1-methylethyl)amino] hydrochloride
- Synonyms
- U 12844A;Isoprenaline impurity A;Norepinephrine Impurity 10;Isoprenaline EP Impurity A;Isoprenaline impurity A CRS;Isoprenaline EP Impurity A HCl;Isoprenaline HCl EP Impurity A;Isoprenaline HCl EP Impurity A HCl;Isoprenaline impurity 1 (hydrochloride);Isoprenaline hydrochloride EP Impurity A
- CBNumber
- CB4912824
- Molecular Formula
- C11H15NO3.ClH
- Formula Weight
- 245.704
- MOL File
- 16899-81-3.mol
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1-(3,4-dihydroxyphenyl)-2-[(1-methylethyl)amino] hydrochloride Property
- Melting point:
- 255-257℃
- storage temp.
- 2-8°C
- Appearance
- White to off-white Solid
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N-Bromosuccinimide Price
Sigma-Aldrich
- Product number
- Y0001577
- Product name
- Isoprenaline impurity A
- Purity
- European Pharmacopoeia (EP) Reference Standard
- Packaging
- 15 mg
- Price
- $236
- Updated
- 2025/07/31
Sigma-Aldrich
- Product number
- S346322
- Product name
- 3',4'-DIHYDROXY-2-(ISOPROPYLAMINO)-ACETOPHENONE HYDROCHLORIDE
- Purity
- Aldrich<sup>CPR</sup>
- Packaging
- 1 unit
- Price
- $185
- Updated
- 2025/07/31
Sigma-Aldrich
- Product number
- Y0001577
- Product name
- Isoprenaline impurity A
- Purity
- European Pharmacopoeia (EP) Reference Standard
- Packaging
- y0001577
- Price
- $220
- Updated
- 2024/03/01
Sigma-Aldrich
- Product number
- S346322
- Product name
- Isoprenaline impurity A
- Purity
- Aldrich
- Packaging
- 50mg
- Price
- $179
- Updated
- 2024/03/01
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1-(3,4-dihydroxyphenyl)-2-[(1-methylethyl)amino] hydrochloride Chemical Properties,Usage,Production
Uses
1-(3,4-Dihydroxyphenyl)-2-[(1-methylethyl)amino]-ethanone is an impurity of Isoprenaline (I874200, HCl salt) which is non-selective beta-adrenergic agonist. Isoprenaline is used in the treatment of bradycardia.
Preparation
Obtained by condensation of a-chloro-3,4- dihydroxy-acetophenone with isopropylamine in isopropanol at 65–70°. The amino ketone which separated was treated with concentrated hydrochloric acid (54%), (46%).
1-(3,4-dihydroxyphenyl)-2-[(1-methylethyl)amino] hydrochloride Preparation Products And Raw materials
Raw materials
Preparation Products
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