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BROMOPRIDE

CAS No.
4093-35-0
Chemical Name:
BROMOPRIDE
Synonyms
Emoril;Viadil;Artomey;Praiden;Plesium;Opridan;Emepride;val13081;BROMOPRID;VAL 13081
CBNumber:
CB8288660
Molecular Formula:
C14H22BrN3O2
Molecular Weight:
344.25
MDL Number:
MFCD00078959
MOL File:
4093-35-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-16 07:06:08
Product description Number Pack Size Price
Bromopride ≥95% 29329 1mg $36
Bromopride ≥95% 29329 5mg $145
Bromopride ≥95% 29329 10mg $236
Bromopride ≥95% 29329 25mg $502
Bromopride TRC-B686645-5MG 5mg $107
More product size

BROMOPRIDE Properties

Melting point 148-150C
Boiling point 435.8±45.0 °C(Predicted)
Density 1.4132 (rough estimate)
refractive index 1.6200 (estimate)
storage temp. 2-8°C
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form Solid
pka 13.84±0.46(Predicted)
color White to Off-White
InChI InChI=1S/C14H22BrN3O2/c1-4-18(5-2)7-6-17-14(19)10-8-11(15)12(16)9-13(10)20-3/h8-9H,4-7,16H2,1-3H3,(H,17,19)
InChIKey GIYAQDDTCWHPPL-UHFFFAOYSA-N
SMILES C(NCCN(CC)CC)(=O)C1=CC(Br)=C(N)C=C1OC
FDA UNII 75473V2YZK
ATC code A03FA04

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H312-H332
Precautionary statements  P280
Hazard Codes  Xn
Risk Statements  20/21/22
Safety Statements  36
WGK Germany  3
RTECS  BZ3280000
NFPA 704
0
3 0

BROMOPRIDE price More Price(47)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 29329 Bromopride ≥95% 4093-35-0 1mg $36 2026-04-30 Buy
Cayman Chemical 29329 Bromopride ≥95% 4093-35-0 5mg $145 2026-04-30 Buy
Cayman Chemical 29329 Bromopride ≥95% 4093-35-0 10mg $236 2026-04-30 Buy
Cayman Chemical 29329 Bromopride ≥95% 4093-35-0 25mg $502 2026-04-30 Buy
TRC TRC-B686645-5MG Bromopride 4093-35-0 5mg $107 2026-06-03 Buy
Product number Packaging Price Buy
29329 1mg $36 Buy
29329 5mg $145 Buy
29329 10mg $236 Buy
29329 25mg $502 Buy
TRC-B686645-5MG 5mg $107 Buy

BROMOPRIDE Chemical Properties,Uses,Production

Description

Bromopride is a dopamine D2 receptor antagonist (Ki = 14 nM). It binds to bovine anterior pituitary membranes with an IC50 value of 2.13 μM. Bromopride inhibits cholinesterase activity in vitro in rat plasma and striatum homogenate (IC50s = 67.8 and 38.4 μM, respectively). It increases serum prolactin levels in rats by 100% when used at a dose of 0.02 mol/kg. Bromopride (2.5 mg/kg) decreases locomotion and rearing in an open field test and impairs acquistion, but not retention, of a conditioned avoidance response in a two-way active conditioned avoidance test in rats.

Chemical Properties

White Solid

Originator

Praiden,Italchemi,Italy,1977

Uses

An antiemetic.Bromopride is used in method and a system for analyzing neuropharmacology of a drug.

Definition

ChEBI: 4-amino-5-bromo-N-[2-(diethylamino)ethyl]-2-methoxybenzamide is a member of benzamides.

Manufacturing Process

To 119 g (0.45 mol) of N-(2-diethylaminoethyl)-2-methoxy-4-aminobenzamide dissolved in 200 cc of acetic acid are added in the cold in small portions 69 g of acetic anhydride (0.45 mol + 50% excess). The starting material is made by esterifying 4-aminosalicylic acid with methanol, then acetylating with acetic anhydride and then methylating with dimethyl sulfate. The solution obtained is heated for 2 hours on a water bath and then boiled for 15 minutes. It is cooled at 25°C. While agitating constantly and maintaining the temperature between 25° and 30°C, there is added to the solution drop by drop 72 g of bromine dissolved in 60 cc of acetic acid. It is agitated for one hour. The mixture obtained is added to one liter of water and the base is precipitated by the addition of 30% soda, The precipitated base is extracted with 40 cc of methylene chloride. After evaporation of the solvent, the residue is boiled for two hours with 390 g of concentrated hydrochloric acid in 780 cc of water. It is cooled, diluted with one liter of water, 12 g of charcoal are added, and the mixture filtered. The base is precipitated with 30% soda. The N-(2- diethylaminoethyl)-2-methoxy-4-amino-5-bromobenzamide formed crystallizes, is centrifuged and washed with water. A yield of 85 g of base having a melting point of 129°-130°C is obtained.
To produce the dihydrochloride, the free base is dissolved in 110 cc of absolute alcohol, 9.6 g of dry hydrochloric acid dissolved in 35 cc of alcohol are added, followed by 2.8 cc of water. The dihydrochloride precipitates, is centrifuged, washed, and dried at 40°C. It was a solid white material having a melting point of 134°-135°C.

Therapeutic Function

Antiemetic

References

[1] M. TONINI. Clinical implications of enteric and central D2 receptor blockade by antidopaminergic gastrointestinal prokinetics[J]. Alimentary Pharmacology & Therapeutics, 2004, 19 4: 379-390. DOI: 10.1111/j.1365-2036.2004.01867.x
[2] HERBERT Y. MELTZER  Rebecca S  Miljana Simonovic. Effects of a series of substituted benzamides on rat prolactin secretion and 3H-spiperone binding to bovine anterior pituitary membranes[J]. Life sciences, 1983, 32 25: Pages 2877-2886. DOI: 10.1016/0024-3205(83)90324-7
[3] A G NASELLO. Differential effects of bromopride and domperidone on cholinesterase activity in rat tissues.[J]. Life sciences, 1995, 56 3: 151-156. DOI: 10.1016/0024-3205(94)00429-v
[4] ANTONIA GLADYS NASELLO  Luciano F F  Maria Luzinete Alves Vanzeler. A Comparison of Bromopride and Domperidone Effects on Rat Conditioned Avoidance and Motor Activity[J]. Basic & Clinical Pharmacology & Toxicology, 1991, 68 1: 46-50. DOI: 10.1111/j.1600-0773.1991.tb01206.x

BROMOPRIDE Preparation Products And Raw materials

Global( 121)Suppliers
Supplier Tel Email Country ProdList Advantage
Xiamen AmoyChem Co., Ltd
+86-86-5926051114 sales@amoychem.com China 6339 58
CONIER CHEM AND PHARMA LIMITED
sales@conier.com China 49906 58
SIMAGCHEM CORP
+86-5922680277 +86-13806087780 sale@simagchem.com China 17339 58
TargetMol Chemicals Inc.
+1-781-999-5354; +1-00000000000 marketing@targetmol.com United States 32431 58
Career Henan Chemica Co
+86-0371-86658258 +86-13203830695 laboratory@coreychem.com China 30203 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +86-189 4982 3763 sales@tnjchem.com China 34526 58
AFINE CHEMICALS LIMITED
+86-571-85134551 +86-18958018566 info@afinechem.com China 15050 58
BOC Sciences
16314854226; +8616314854226 inquiry@bocsci.com United States 19852 58
Alfa Chemistry
+1-5166625404; Info@alfa-chemistry.com United States 20000 58
Shaanxi Didu New Materials Co. Ltd
+86-86-17392712779 +86-13289823923 1090@dideu.com China 8651 58

View Lastest Price from BROMOPRIDE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Bromopride pictures 2026-07-16 Bromopride
4093-35-0
$56.00-179.00 99.95% 10g TargetMol Chemicals Inc.
Bromopride pictures 2026-07-15 Bromopride
4093-35-0
$56.00-179.00 99.95% 10g TargetMol Chemicals Inc.
  • Bromopride pictures
  • Bromopride
    4093-35-0
  • $56.00-179.00
  • 99.95%
  • TargetMol Chemicals Inc.
  • Bromopride pictures
  • Bromopride
    4093-35-0
  • $56.00-179.00
  • 99.95%
  • TargetMol Chemicals Inc.

BROMOPRIDE Spectrum

4-Amino-5-bromo-N-[2-(diethylamino)ethyl]-2-methoxybenzamide,Emepride,Emoril,Viadil BROMOPRID 2-Methoxy-4-aMino-5-broMo-N,N-diethylaMinoethylbenzaMide Opridan Plesium Praiden 4-azanyl-5-bromo-N-(2-diethylaminoethyl)-2-methoxy-benzamide 4-amino-5-bromo-n-(2-(diethylamino)ethyl)-2-methoxy-benzamid 4-amino-5-bromo-n-(2-(diethylamino)ethyl)-o-anisamid 4-Amino-5-bromo-N-[2-(diethylamino)ethyl]-2-methoxybenzamide Artomey Benzamide, 4-amino-5-bromo-N-[2-(diethylamino)ethyl]-2-methoxy- Bromoprida Emepride Emoril n-(diethylaminoethyl)-2-methoxy-4-amino-5-bromobenzamide o-Anisamide, 4-amino-5-bromo-N-[2-(diethylamino)ethyl]- VAL 13081 val13081 Valopride Viadil 4-AMINO-5-BROMO-N-[2-(DIETHYL-AMINO)ETHYL-O-ANISAMIDE BROMOPRIDE BromoprideQ: What is Bromopride Q: What is the CAS Number of Bromopride Q: What is the storage condition of Bromopride Q: What are the applications of Bromopride Inhibitor,Bromopride,Dopamine Receptor,inhibit Bromopride in methanol Bromopride, 10 mM in DMSO Bromothyroxine Bromopride Impurity 8 4093-35-0 C14H22BrN3O2 BI - BZ Alphabetic Analytical Chromatography Product Catalog Analytical Standards Intermediates & Fine Chemicals Pharmaceuticals Amines Aromatics EMEPRIDE