Technology Transfer Pitfalls in Intermediate Projects: Avoid Costly Mistakes
This article breaks down the 4 most costly mistakes — including incomplete documentation and ignored scalability — with verified industry data and real cases.
4-AMino-5-Methylpyridin-2-ol; 4-AMino-5-Methyl-2-(1H)-pyridinone;4-amino-5-methylpyridone
CAS:95306-64-2
Chemical Formula:C6H8N2O
MW:124.14
Availability: R&D; Commercialization
⬤ CAS No.95306-64-2
⬤ Packaging type:
20kg barrel;5kg barrel;1kg bag;500g bag ; Customized Packaging
| English name | 4-amino-5-methyl-2-hydroxypyridine |
| CAS No. | 95306-64-2 |
| Chemical formula | C6H8N2O |
| Molecular weight | 124.14 |
| Related categories | Pyridine series; fenerenone intermediates; chemical reagents |
| Mol | 95306-64-2.mol |
| EINECS | 682-818-3 |
| Boiling point | 291.0±33.0℃ (760 Torr) |
| Density | 1.137±0.06 g/cm3 (20 ºC 760 Torr) |
| Vapor pressure | 0-0Pa at 20-50℃ |
| Flash point | 129.8±25.4℃ |
| Storage conditions | 2-8°C(protect from light) |
| LogP | -0.51 at 20℃ and pH6.3 |
| Acidity coefficient (pKa) | 11.90±0.10(Predicted) |
| CAS | 95306-64-2 |
| Hazard symbols | GHS07 |
| Hazard description | H302, H315, H319, H335 |
| Storage conditions | Keep in dark place, Sealed in dry, 2-8°C |
| Physical state | Solid (usually light yellow powder) |
| stability | Stable under recommended storage conditions, avoid contact with strong oxidants, acids and other incompatible substances |
| Ecotoxicity | May be harmful to aquatic life, please refer to ecotoxicity data for details |
| Special considerations | Avoid contact with strong oxidants, acids, etc.; wear appropriate personal protective equipment; operate in a well-ventilated area |
| Introduction | It is an important raw material for synthesizing new drugs such as finerenone. |
| Uses |
Pharmaceutical intermediates: It can be used to synthesize a variety of biologically active drug molecules, such as finerenone; Organic synthesis reagents: Since the alcohol hydroxyl group in its structure can undergo nucleophilic substitution reactions under alkaline conditions, it can be used to prepare polysubstituted pyridine compounds; Scientific research: In the research of chemistry, biochemistry, and medicinal chemistry, 4-amino-5-methyl-2-hydroxypyridine is also often used as a model compound or reaction substrate. |
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This article breaks down the 4 most costly mistakes — including incomplete documentation and ignored scalability — with verified industry data and real cases.
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