119812-29-2
3-[(Dimethylamino)methyl]-1,2,3,9-tetrahydro-9-methyl-4H-carbazol-4-one hydrochloride
CAS: 119812-29-2
Molecular Formula: C16H20N2O.ClH
119812-29-2 - Names and Identifiers
119812-29-2 - Physico-chemical Properties
| Molecular Formula | C16H20N2O.ClH |
| Molar Mass | 292.81 |
| Appearance | neat |
| BRN | 11612579 |
| Storage Condition | Room Temprature |
119812-29-2 - Risk and Safety
| Hazard Symbols | T - Toxic |
| Risk Codes | 25 - Toxic if swallowed |
| Safety Description | 45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
| UN IDs | UN 2923 6.1(8) / PGIII |
| WGK Germany | 3 |
| HS Code | 2933997500 |
119812-29-2 - Introduction
3-[(Dimethylamino)methyl]-1,2,3, hydrochloride is a chemical substance with the chemical name 3-[(Dimethylamino)methyl]-1,3, hydrochloride, often referred to as EP impurity A.
1. Nature:
EP impurity A is A white crystalline solid, easily soluble in water and organic solvents.
2. Use:
EP impurity A is mainly used in the pharmaceutical industry as an intermediate of the antidepressant ondansetron. It plays an important role in the synthesis of ondansetron, helping to control the purity and quality of the product.
3. Preparation method:
The method of preparing EP impurity A can be achieved by chemical synthesis. One common approach is to perform the synthesis using known synthetic routes, including a series of reaction steps and purification processes. Specific synthesis details need to be carried out under laboratory conditions.
4. Safety Information:
The safety of EP impurity A needs to be evaluated based on relevant safety data and laboratory experiments. When using and handling, it is necessary to pay attention to personal protective measures, such as wearing gloves, wearing appropriate protective clothing and eye protection. In addition, comply with relevant regulations for the storage and handling of chemicals, and avoid contact with skin, eyes, and inhalation of their dust or gases. During operation, comprehensive laboratory safety procedures should be followed. Appropriate waste disposal should also be carried out if necessary. Please consult the relevant safety data sheets and documents for more detailed information.
1. Nature:
EP impurity A is A white crystalline solid, easily soluble in water and organic solvents.
2. Use:
EP impurity A is mainly used in the pharmaceutical industry as an intermediate of the antidepressant ondansetron. It plays an important role in the synthesis of ondansetron, helping to control the purity and quality of the product.
3. Preparation method:
The method of preparing EP impurity A can be achieved by chemical synthesis. One common approach is to perform the synthesis using known synthetic routes, including a series of reaction steps and purification processes. Specific synthesis details need to be carried out under laboratory conditions.
4. Safety Information:
The safety of EP impurity A needs to be evaluated based on relevant safety data and laboratory experiments. When using and handling, it is necessary to pay attention to personal protective measures, such as wearing gloves, wearing appropriate protective clothing and eye protection. In addition, comply with relevant regulations for the storage and handling of chemicals, and avoid contact with skin, eyes, and inhalation of their dust or gases. During operation, comprehensive laboratory safety procedures should be followed. Appropriate waste disposal should also be carried out if necessary. Please consult the relevant safety data sheets and documents for more detailed information.
Last Update：2024-04-09 20:52:54
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Product Name: 3-[(Dimethylamino)methyl]-1,2,3,9-tetrahydro-9-methyl-4H-carbazol-4-one hydrochloride Visit Supplier Webpage Request for quotation
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CAS: 119812-29-2
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