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Sulpiride

CAS No.
15676-16-1
Chemical Name:
Sulpiride
Synonyms
Abilit;Dobren;Meresa;Eglonyl;Guastil;Miradol;Neogama;Omperan;Splotin;Synedil
CBNumber:
CB4141314
Molecular Formula:
C15H23N3O4S
Molecular Weight:
341.43
MDL Number:
MFCD00055061
MOL File:
15676-16-1.mol
MSDS File:
SDS
Last updated:2024-11-20 11:41:24

Sulpiride Properties

Melting point 178-180°
alpha D25 -66.8° (c = 0.5 in DMF)
Density 1.2375 (rough estimate)
refractive index 1.6320 (estimate)
storage temp. 2-8°C
solubility 45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 8.0 mg/mL
form powder
pka pKa1 9.00, pKa2 10.19(at 25℃)
color yellow
Water Solubility <0.21g/L(25 ºC)
λmax 232nm(EtOH)(lit.)
Merck 14,8989
InChIKey BGRJTUBHPOOWDU-UHFFFAOYSA-N
LogP 0.57
CAS DataBase Reference 15676-16-1(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 7MNE9M8287
ATC code N05AL01
NIST Chemistry Reference Sulpiride(15676-16-1)
EPA Substance Registry System Sulpiride (15676-16-1)

Pharmacokinetic data

Protein binding 40%
Excreted unchanged in urine 90-95%
Volume of distribution 1.2-1.7(L/kg)
Biological half-life 8-9 / 26

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS08
Signal word  Warning
Hazard statements  H361
Precautionary statements  P280
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  2
RTECS  BZ3400000
HS Code  2933.99.6100
Toxicity LD50 in mice (mg/kg): 170 i.p.; 2250 orally (Dostert)

Sulpiride price More Price(35)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich S8010 (±)-Sulpiride 15676-16-1 25g $117 2024-03-01 Buy
Sigma-Aldrich S8010 (±)-Sulpiride 15676-16-1 100g $414 2024-03-01 Buy
Sigma-Aldrich BP679 Sulpiride British Pharmacopoeia (BP) Reference Standard 15676-16-1 100MG $259 2023-06-20 Buy
TCI Chemical S0501 (±)-Sulpiride >98.0%(HPLC)(T) 15676-16-1 5g $36 2024-03-01 Buy
TCI Chemical S0501 (±)-Sulpiride >98.0%(HPLC)(T) 15676-16-1 25g $144 2024-03-01 Buy
Product number Packaging Price Buy
S8010 25g $117 Buy
S8010 100g $414 Buy
BP679 100MG $259 Buy
S0501 5g $36 Buy
S0501 25g $144 Buy

Sulpiride Chemical Properties,Uses,Production

Chemical Properties

Sulpiride is White Solid

Originator

Dogmatil,Delagrange,France,1969

Uses

dopamine receptor antagonist, antipsychotic

Uses

Sulpiride possesses moderate neuroleptic activity along with some stimulating and antidepressant effects. It has antiemetic, moderately cataleptogenic, and antiserotonin action. It facilitates increased blood flow in the stomach. It speeds up the restorative processes in tissues. It is used for schizophrenia, depression, migraines, disturbance of behavioral functions, and stomach and duodenal ulcers.

Uses

Sulpiride is an antipsychotic drug used in the treatment of Schozophrenia and depression.

Definition

Sulpiride is a member of the class of benzamides obtained from formal condensation between the carboxy group of 2-methoxy-5-sulfamoylbenzoic acid and the primary amino group of (1-ethylpyrrolidin-2-yl)methylamine.

Manufacturing Process

1-Ethyl-2-aminomethylpyrrolidine is reacted with 2-methoxy-5- sulfamoylbenzoic acid to give sulpiride.

brand name

Dogmatyl (Laboratoires Delagrange, France).

Therapeutic Function

Tranquilizer, Digestive aid

Biological Activity

Standard D 2 -like dopamine receptor antagonist.

Biochem/physiol Actions

(±)-Sulpiride is a D2 dopamine antagonist and an effective treatment for schizophrenia when used in combination with clozapine, a relatively weak D2-dopaminergic antagonist. It is an antipsychotic agent and also exhibits neuroleptic properties but poorly penetrates the central nervous system.45,46

Clinical Use

Antipsychotic:
Acute and chronic schizophrenia

Synthesis

Sulpiride, N-[(1-ethyl-2-pirrolidinylmethyl]-5-sulfamoyl-O-anizamide (6.7.2), is synthesized from 5-aminosulfosalycilic acid. Methylating this with dimethylsulfate gives 2-methoxy-5-aminosulfonylbenzoic acid (6.7.1), which is transformed into an amide using 2-aminomethyl-1-ethylpyrrolidine as amine components and carbonyl-1,1??-bisimidazole as a condensing agent [70¨C74].

Synthesis_15676-16-1

Drug interactions

Potentially hazardous interactions with other drugs
Anaesthetics: enhanced hypotensive effect.
Analgesics: increased risk of convulsions with tramadol; enhanced hypotensive and sedativeeffects with opioids; increased risk of ventricular arrhythmias with methadone.
Anti-arrhythmics increased risk of ventricular arrhythmias with anti-arrhythmics that prolong the QT interval, e.g. procainamide, disopyramide and amiodarone - avoid with amiodarone.
Antibacterials: increased risk of ventricular arrhythmias with moxifloxacin and parenteral erythromycin - avoid with moxifloxacin.
Antidepressants: possibly increased risk of ventricular arrhythmias and antimuscarinic side effects with tricyclics - avoid.
Antiepileptics: antagonism (convulsive threshold lowered).
Antimalarials: avoid with artemether/lumefantrine.
Antipsychotics: increased risk of ventricular arrhythmias with droperidol, haloperidol and pimozide - avoid; possible increased risk of ventricular arrhythmias with risperidone.
Antivirals: concentration possibly increased by ritonavir.
Anxiolytics and hypnotics: increased sedative effects.
Atomoxetine: increased risk of ventricular arrhythmias.
Beta-blockers: enhanced hypotensive effect; increased risk of ventricular arrhythmias with sotalol.
Cytotoxics: increased risk of ventricular arrhythmias with vandetanib - avoid; increased risk of ventricular arrhythmias with arsenic trioxide.
Diuretics: enhanced hypotensive effect.
Lithium: increased risk of extrapyramidal side effects and possibly neurotoxicity.
Pentamidine: increased risk of ventricular arrhythmias.

Metabolism

Sulpiride undergoes little metabolism.
95% of a dose is excreted in the urine and faeces, mainly as unchanged drug.

storage

Room temperature

Sulpiride Preparation Products And Raw materials

Global( 315)Suppliers
Supplier Tel Email Country ProdList Advantage
Xiamen Wonderful Bio Technology Co., Ltd.
+8613043004613 Sara@xmwonderfulbio.com China 283 58
Nantong Guangyuan Chemicl Co,Ltd
+undefined17712220823 admin@guyunchem.com China 615 58
Hangzhou Hyper Chemicals Limited
+86-0086-57187702781 +8613675893055 info@hyper-chem.com China 295 58
Shaanxi TNJONE Pharmaceutical Co., Ltd
+8618092446649 sarah@tnjone.com China 1143 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806 sales@capot.com China 29791 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21634 55
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418679 +8618949832763 info@tnjchem.com China 2986 55
Xiamen AmoyChem Co., Ltd
+86-86-5926051114 +8618959220845 sales@amoychem.com China 6383 58
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22963 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49374 58

View Lastest Price from Sulpiride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Sulpiride pictures 2024-11-27 Sulpiride
15676-16-1
US $0.00 / KG 1KG 98%min 300KG/month WUHAN FORTUNA CHEMICAL CO., LTD
Sulpiride pictures 2024-11-19 Sulpiride
15676-16-1
US $36.00-64.00 / mg 100% 10g TargetMol Chemicals Inc.
Sulpiride pictures 2024-11-19 Sulpiride
15676-16-1
US $36.00-64.00 / mg 100% 10g TargetMol Chemicals Inc.
  • Sulpiride pictures
  • Sulpiride
    15676-16-1
  • US $0.00 / KG
  • 98%min
  • WUHAN FORTUNA CHEMICAL CO., LTD
  • Sulpiride pictures
  • Sulpiride
    15676-16-1
  • US $36.00-64.00 / mg
  • 100%
  • TargetMol Chemicals Inc.
  • Sulpiride pictures
  • Sulpiride
    15676-16-1
  • US $36.00-64.00 / mg
  • 100%
  • TargetMol Chemicals Inc.

Sulpiride Spectrum

R.D. 1403 rac Sulpiride (RS)-(+/-)-SULPIRIDE (RS)-(+/-)-5-AMINOSULFONYL-N-[(1-ETHYL-2-PYRROLIDINYL)METHYL]-2-METHOXYBENZAMIDE (+/-)-SULPIRIDE SULPIRIDE Abilit Aiglonyl Benzamide, 5-(aminosulfonyl)-N-[(1-ethyl-2-pyrrolidinyl)methyl]-2-methoxy- Coolspan Dobren Dogmatil Dogmatyl Dolmatil Eglonyl Guastil Levobren l-Forms: levosulpiride Meresa Miradol Mirbanil Misulvan N-((1-Ethyl-2-pyrrolidinyl)methyl)-2-methoxy-5-sulfamoylbenzamide n-((1-ethyl-2-pyrrolidinyl)methyl)-5-sulfamoyl-o-anisamid N-((1-Ethyl-2-pyrrolidinyl)methyl)-5-sulfamoyl-o-anisamide Neogama o-Anisamide, N-((1-ethyl-2-pyrrolidinyl)methyl)-5-sulfamoyl- Omperan Pyrikappl Pyrkappl Sulpiride COS (+/-)-N-1-(ETHYLPYRROLIDIN-2-YLMETHYL)-2-METHOXY-5-SULFAMOYLBENZAMIDE [+/-]-N-1-[ETHYLPYRROLIDIN-2-YLMETHYL]-2-METHOXY-5-SULFAMOYLBENZAMIDE r.d.1403 Sernevin Splotin Sulpirid Sulpitil Sulpyrid Sursumid Synedil 5-(aminosufonyl)-n-[(1-ethyl-2-pyrrolidinyl)methyl]-2-methoxybenzamide (+/-)-5-AMINOSULFONYL-N-([1-ETHYL-2-PYRROLIDINYL)METHYL]-2-METHOXY-BENZAMIDE 5-(AMINOSULFONYL)-N-[(1-ETHYL-2-PYRROLIDINYL)METHYL]-2-METHOXY-BENZAMIDE Dogmatilum Benzamide, 5-(aminosulfonyl)-N-[(1-ethyl-2-pyrrolidinyl)methyl]-2-methoxy- (9CI) DL-Sulpiride N-(1-Ethyl-2-pyrrolidinylmethyl)-2-methoxy-5-sulfamidobenzamide o-Anisamide, N-[(1-ethyl-2-pyrrolidinyl)methyl]-5-sulfamoyl- (8CI) (+/-)SULPIRIDE DOPAMINE D2 ANTAGONIS (±)-N-1-(Ethylpyrrolidin-2-ylmethyl)-2-methoxy-5-sulfamoylbenzamide, (±)-5-(Aminosulfonyl)-N-[(1-ethyl-2-pyrrolidinyl)methyl]-2-methoxybenzamide (±)-Sulpiride,(±)-5-(Aminosulfonyl)-N-[(1-ethyl-2-pyrrolidinyl)methyl]-2-methoxybenzamide, (±)-N-1-(Ethylpyrrolidin-2-ylmethyl)-2-methoxy-5-sulfamoylbenzamide (+)-N-[[(2R)-1-Ethyl-2-pyrrolidinyl]methyl]-5-sulfamoyl-2-methoxybenzamide ulpiride N-{[(2S)-1-ethylpyrrolidin-2-yl]Methyl}-2-Methoxy-5-sulfaMoylbenzaMide 2-[8-[(2-Benzothiazolylamino)carbonyl]-3,4-dihydro-2(1H)-isoquinolinyl]-5-[3-[4-[3-(dimethylamino)-1-propyn-1-yl]-2-fluorophenoxy]propyl]-4-thiazolecarboxylic Acid Hydrochloride N-[[(2R)-1-ethyl-2-pyrrolidin-1-iumyl]methyl]-2-methoxy-5-sulfamoylbenzamide Sulpiride CRS