China (Mainland)
Premiumsupplier 
Amisulpride 71675-85-9 CAS NO.71675-85-9
- Min.Order: 1 Kilogram
- Payment Terms: L/C,D/A,D/P,T/T,
- Product Details
Keywords
- 71675-85-9
- 71675-85-9
- C17H27N3O4S
Quick Details
- ProName: Amisulpride 71675-85-9
- CasNo: 71675-85-9
- Molecular Formula: C17H27N3O4S
- Appearance: White or off-white Solid
- DeliveryTime: 20day
- PackAge: According to the demand of customer
- Port: shanghai
- ProductionCapacity: 20 Metric Ton/Month
- Purity: 98%
- Storage: Sealed, dry, microtherm , avoid light ...
- Transportation: According to the demand of customer
- LimitNum: 1 Kilogram
Superiority
| Amisulpride Basic information |
| Product Name: | Amisulpride |
| Synonyms: | 4-AMINO-N-[(1-ETHYL-2-PYRROLIDINYL)METHYL]-5-(ETHYLSULFONYL)-2-METHOXYBENZAMIDE;AMISULPRIDE;AMINOSULTOPRIDE;DAN-2163;DENIBAN;SOCIAN;SOLIAN;4-amino-n-((1-ethyl-2-pyrrolidinyl)methyl)-5-(ethylsulfonyl)-2-methoxybenzam |
| CAS: | 71675-85-9 |
| MF: | C17H27N3O4S |
| MW: | 369.48 |
| EINECS: | 275-831-7 |
| Product Categories: | Active Pharmaceutical Ingredients;Antipsychotic;Drug Analogues;Intermediates & Fine Chemicals;Pharmaceuticals;Dopamine receptor;DENIBAN |
| Mol File: | 71675-85-9.mol |
|
|
|
| Amisulpride Chemical Properties |
| mp | 124-128 |
| storage temp. | 2-8°C |
| solubility | DMSO: ≥5 mg/mL |
| form | solid |
| color | white |
| CAS DataBase Reference | 71675-85-9(CAS DataBase Reference) |
| Safety Information |
| Hazard Codes | Xn |
| Risk Statements | 22 |
| Safety Statements | 22-24/25 |
| WGK Germany | 3 |
| RTECS | CV2308701 |
| MSDS Information |
| Provider | Language |
|---|---|
| Amisulpride | English |
| SigmaAldrich | English |
| Amisulpride Usage And Synthesis |
| Chemical Properties | Off-White Solid |
| Usage | Neuroleptic agent, an analogue of sulpiride. Used as an antipsychotic. Dopamine receptor antagonist |
| Usage | Amisulpride is a neuroleptic agent, an analogue of Sulpiride (S689145). Amisulpride is used as an antipsychotic. Amisulpride is a dopamine receptor antagonist. |
| Biological Activity | Potent, selective dopamine D 2 and D 3 receptor antagonist. K i values are 2.8 and 3.2 nM respectively for human D 2 and D 3 and > 1000 nM for human D 1 , D 4 and D 5 receptors. Shows selectivity for presynaptic dopamine autoreceptors at low doses and blocks postsynaptic D 2 /D 3 receptors at higher doses. Preferentially interacts with limbic D 2 -like receptors in vivo . Atypical antipsychotic/antischizophrenic agent with limited extrapyrimidal side effects and a profile distinct from that of haloperidol and remoxipride. |
Details
| Amisulpride Basic information |
| Product Name: | Amisulpride |
| Synonyms: | 4-AMINO-N-[(1-ETHYL-2-PYRROLIDINYL)METHYL]-5-(ETHYLSULFONYL)-2-METHOXYBENZAMIDE;AMISULPRIDE;AMINOSULTOPRIDE;DAN-2163;DENIBAN;SOCIAN;SOLIAN;4-amino-n-((1-ethyl-2-pyrrolidinyl)methyl)-5-(ethylsulfonyl)-2-methoxybenzam |
| CAS: | 71675-85-9 |
| MF: | C17H27N3O4S |
| MW: | 369.48 |
| EINECS: | 275-831-7 |
| Product Categories: | Active Pharmaceutical Ingredients;Antipsychotic;Drug Analogues;Intermediates & Fine Chemicals;Pharmaceuticals;Dopamine receptor;DENIBAN |
| Mol File: | 71675-85-9.mol |
|
|
|
| Amisulpride Chemical Properties |
| mp | 124-128 |
| storage temp. | 2-8°C |
| solubility | DMSO: ≥5 mg/mL |
| form | solid |
| color | white |
| CAS DataBase Reference | 71675-85-9(CAS DataBase Reference) |
| Safety Information |
| Hazard Codes | Xn |
| Risk Statements | 22 |
| Safety Statements | 22-24/25 |
| WGK Germany | 3 |
| RTECS | CV2308701 |
| MSDS Information |
| Provider | Language |
|---|---|
| Amisulpride | English |
| SigmaAldrich | English |
| Amisulpride Usage And Synthesis |
| Chemical Properties | Off-White Solid |
| Usage | Neuroleptic agent, an analogue of sulpiride. Used as an antipsychotic. Dopamine receptor antagonist |
| Usage | Amisulpride is a neuroleptic agent, an analogue of Sulpiride (S689145). Amisulpride is used as an antipsychotic. Amisulpride is a dopamine receptor antagonist. |
| Biological Activity | Potent, selective dopamine D 2 and D 3 receptor antagonist. K i values are 2.8 and 3.2 nM respectively for human D 2 and D 3 and > 1000 nM for human D 1 , D 4 and D 5 receptors. Shows selectivity for presynaptic dopamine autoreceptors at low doses and blocks postsynaptic D 2 /D 3 receptors at higher doses. Preferentially interacts with limbic D 2 -like receptors in vivo . Atypical antipsychotic/antischizophrenic agent with limited extrapyrimidal side effects and a profile distinct from that of haloperidol and remoxipride. |