| Company Name: |
BOC Sciences |
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1-631-485-4226; 16314854226 |
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alpha-Bromoisobutyric acid manufacturers
- Pheniprazine
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- $1520.00
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2026-05-11
- CAS:55-52-7
- Purity:
- Supply Ability: 10g
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| | alpha-Bromoisobutyric acid Basic information |
| Product Name: | alpha-Bromoisobutyric acid | | Synonyms: | HYDRAZINE,(ALPHA-METHYLPHENETHYL)-;PHENYLISOPROPYLHYDRAZINE;BETA-PHENYLISOPROPYLHYDRAZINE;2-HYDRAZINOPROPYLBENZENE;(1-Methyl-2-phenylethyl)hydrazine;JB-516;Phenizine;1-phenylpropan-2-ylhydrazine | | CAS: | 55-52-7 | | MF: | C9H14N2 | | MW: | 150.22 | | EINECS: | 200-236-6 | | Product Categories: | | | Mol File: | 55-52-7.mol |  |
| | alpha-Bromoisobutyric acid Chemical Properties |
| Melting point | 25°C | | Boiling point | 261.79°C (rough estimate) | | density | 0.9372 (rough estimate) | | refractive index | 1.6210 (estimate) | | pka | 8.00±0.70(Predicted) |
| Toxicity | LD50 orl-rat: 34 mg/kg 27ZQAG -,353,72 |
| | alpha-Bromoisobutyric acid Usage And Synthesis |
| Originator | Catron ,Lakeside, US,1959 | | Definition | ChEBI: Pheniprazine is a member of amphetamines. | | Manufacturing Process | A solution containing 741 g (5.0 mols) of 1 -phenyl-2-propylidenylhydrazine, 300 g (5.0 mols) of glacial acetic acid and 900 cc of absolute ethanol was subjected to hydrogenation at 1,875 psi of hydrogen in the presence of 10 g of platinum oxide catalyst and at a temperature of 30°C to 50°C (variation due to exothermic reaction). The catalyst was removed by filtration and the solvent and acetic acid were distilled. The residue was taken up in water and made strongly alkaline by the addition of solid potassium hydroxide. The alkaline mixture was extracted with ether and the ether extracts dried with potassium carbonate. The product was collected by fractional distillation, BP 85°C (0.30 mm); yield 512 g (68%).
The hydrochloride salt was formed in a mixture of 1:10 isopropyl alcohol:diisopropyl ether and recrystallized from acetonitrile, yield 87%, MP 124°C to 125°C. | | Brand name | Catron Hydrochloride (Marion Merrell Dow). | | Therapeutic Function | Antihypertensive | | Safety Profile | Poison by ingestion, intraperitoneal, subcutaneous, and intravenous routes. Human systemic effects by an unspecified route: visual field effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx. |
| | alpha-Bromoisobutyric acid Preparation Products And Raw materials |
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