1-PHENYLPIPERAZINE HYDROCHLORIDE
1-phenylpiperazinium chloride
CAS: 2210-93-7
Molecular Formula: C10H15ClN2
1-PHENYLPIPERAZINE HYDROCHLORIDE - Names and Identifiers
| Name | 1-phenylpiperazinium chloride |
| Synonyms | TIMTEC-BB SBB003556 PHENYL PIPERAZINE HCL 1-PHENYLPIPERAZINE HCL 1-phenylpiperazinium chloride 1-phenyl-piperazinhydrochloride 1-phenylpiperazine hydrochloride 1-PHENYLPIPERAZINE HYDROCHLORIDE N-PHENYLPIPERAZINE HYDROCHLORIDE 1-PHENYLPIPERAZINE MONOHYDROCHLORIDE |
| CAS | 2210-93-7 |
| EINECS | 218-646-9 |
| InChI | InChI=1/C10H14N2.ClH/c1-2-4-10(5-3-1)12-8-6-11-7-9-12;/h1-5,11H,6-9H2;1H |
1-PHENYLPIPERAZINE HYDROCHLORIDE - Physico-chemical Properties
| Molecular Formula | C10H15ClN2 |
| Molar Mass | 198.69 |
| Density | 0.985(20.0000℃) |
| Melting Point | 247-250°C(lit.) |
| Boling Point | 287.2°C at 760 mmHg |
| Flash Point | 138.3°C |
| Vapor Presure | 0.00252mmHg at 25°C |
| Storage Condition | Room Temprature |
| MDL | MFCD00012758 |
1-PHENYLPIPERAZINE HYDROCHLORIDE - Risk and Safety
| Hazard Symbols | T - Toxic |
| Risk Codes | R23/24/25 - Toxic by inhalation, in contact with skin and if swallowed. R36/37/38 - Irritating to eyes, respiratory system and skin. R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S28 - After contact with skin, wash immediately with plenty of soap-suds. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
| UN IDs | UN 2811 6.1/PG 3 |
| WGK Germany | 3 |
| RTECS | TM2640000 |
| HS Code | 29335990 |
| Hazard Class | 6.1 |
| Packing Group | III |
1-PHENYLPIPERAZINE HYDROCHLORIDE - Introduction
1-phenylpiperazinium chloride is an organic compound with the chemical structural formula C11H15ClN2. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
1-phenylpiperazinium chloride is a solid, usually white crystalline or crystalline powder. It has high solubility in water and can be dissolved into a colorless and transparent solution. The compound is stable at room temperature and is not easily decomposed by volatilization.
Use:
1-phenylpiperazinium chloride has certain application value in the field of medicine. It is used as a pharmaceutical intermediate for the preparation of some antipsychotic drugs, sedative drugs and antidepressant drugs.
Method:
A common method for preparing 1-phenylpiperazinium chloride is through the synthesis of piperazine compounds followed by Arylation. The specific steps are as follows:
1. Piperazine and phenyl reagent (such as bromobenzene, fluorobenzene, etc.) reaction, the corresponding substituted piperazine compounds.
2. The substituted piperazine compound is reacted with hydrochloric acid to generate 1-phenylpiperazinium chloride.
3. Purify and crystallize to obtain pure 1-phenylpiperazinium chloride.
Safety Information:
Although there is no clear safety data report to provide information on 1-phenylpiperazinium chloride, as an organic compound, safety measures should be taken to use it. Direct contact with the compound may cause irritation and inhalation or ingestion should be avoided. Wear appropriate protective equipment during operation and avoid contact with skin, eyes and respiratory tract. Properly store and avoid mixing with oxidants, acids, alkalis and other substances. When using and handling, please follow the laboratory's safe operating procedures. When handling any chemical substance, be sure to refer to and comply with the safety data sheet for that substance.
Nature:
1-phenylpiperazinium chloride is a solid, usually white crystalline or crystalline powder. It has high solubility in water and can be dissolved into a colorless and transparent solution. The compound is stable at room temperature and is not easily decomposed by volatilization.
Use:
1-phenylpiperazinium chloride has certain application value in the field of medicine. It is used as a pharmaceutical intermediate for the preparation of some antipsychotic drugs, sedative drugs and antidepressant drugs.
Method:
A common method for preparing 1-phenylpiperazinium chloride is through the synthesis of piperazine compounds followed by Arylation. The specific steps are as follows:
1. Piperazine and phenyl reagent (such as bromobenzene, fluorobenzene, etc.) reaction, the corresponding substituted piperazine compounds.
2. The substituted piperazine compound is reacted with hydrochloric acid to generate 1-phenylpiperazinium chloride.
3. Purify and crystallize to obtain pure 1-phenylpiperazinium chloride.
Safety Information:
Although there is no clear safety data report to provide information on 1-phenylpiperazinium chloride, as an organic compound, safety measures should be taken to use it. Direct contact with the compound may cause irritation and inhalation or ingestion should be avoided. Wear appropriate protective equipment during operation and avoid contact with skin, eyes and respiratory tract. Properly store and avoid mixing with oxidants, acids, alkalis and other substances. When using and handling, please follow the laboratory's safe operating procedures. When handling any chemical substance, be sure to refer to and comply with the safety data sheet for that substance.
Last Update：2024-04-09 20:15:17
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View History
1-PHENYLPIPERAZINE HYDROCHLORIDE
鞘磷酯酶 来源于金黄色葡萄球菌
C-(1H-Pyrazol-3-yl)-methylamine dihydrochoride
CHLORDIMEFORM HCL
D-PLUS-MELEZITOSE HYDRATE
NEVER IN MITOSIS GENE A-RELATED KINASE 7
4-[2-Oxo-5-[(2-propynyloxy)methyl]oxazolidin-3-yl]benzoic acid ethyl ester
Ethyl3-endo-aminobicyclo[2.2.1]hept-5-ene-2-endo-carboxylateHCl
Potassium 1-(2-methoxyethyl)-1h-pyrazole-4-carboxylate
Ethyl uracil-5-carboxylate 5-Carbethoxyuracil
鞘磷酯酶 来源于金黄色葡萄球菌
C-(1H-Pyrazol-3-yl)-methylamine dihydrochoride
CHLORDIMEFORM HCL
D-PLUS-MELEZITOSE HYDRATE
NEVER IN MITOSIS GENE A-RELATED KINASE 7
4-[2-Oxo-5-[(2-propynyloxy)methyl]oxazolidin-3-yl]benzoic acid ethyl ester
Ethyl3-endo-aminobicyclo[2.2.1]hept-5-ene-2-endo-carboxylateHCl
Potassium 1-(2-methoxyethyl)-1h-pyrazole-4-carboxylate
Ethyl uracil-5-carboxylate 5-Carbethoxyuracil