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25614-03-3

Bromocriptine

CAS: 25614-03-3

Molecular Formula: C32H40BrN5O5

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25614-03-3 - Names and Identifiers

Name Bromocriptine
Synonyms 6,18-trione
Bromocriptine
(5-alpha)-ropyl)
2-bromoergocryptine
2-bromo-ergocryptin
2-bromo-alpha-ergocryptine
2-bromo-12-hydroxy-2-(1-methylethyl)-5-alpha-(2-methylpropyl)ergotamin-3
CAS 25614-03-3
EINECS 247-128-5

25614-03-3 - Physico-chemical Properties

Molecular FormulaC32H40BrN5O5
Molar Mass654.59
Density1.2734 (rough estimate)
Melting Point215-218° (dec)
Boling Point891.3±65.0 °C(Predicted)
Water Solubility2.07mg/L(temperature not stated)
pKapKa 4.90±0.05(80% MCS t = RT) (Uncertain)
Refractive Index1.6400 (estimate)
Physical and Chemical PropertiesChemical properties white crystalline powder. Melting point 215-218 ℃ (decomposition).
UseUses the product has the Excitatory effect of dopamine receptors. Through the blood-brain barrier, into the central nervous system, dopamine receptor activation and inhibition of prolactin and growth hormone secretion. It is clinically used for Parkinson's disease, Acromegaly and galactorrhea.

25614-03-3 - Upstream Downstream Industry

Raw MaterialsBROMOSUCCINIC ACID
ALPHA-ERGOCRYPTINE
N-Bromosuccinimide

25614-03-3 - Nature

specific rotation D20 -195° (c = 1 in methylene chloride)
Last Update:2024-04-10 22:29:15

25614-03-3 - Uses and synthesis methods

overview

Bromocriptine is a specific dopamine receptor agonist of the hypothalamus and pituitary gland, which can directly act on the adenohypophysis and inhibit the secretion of prolactin. It is suitable for use in cycles using nolon derivatives.

production method

It is obtained by the reaction of ergocriptine and N-bromosuccinate imine.

category

Toxic substances

acute toxicity

High toxicity

stimulus data

intravenous-rat LD50: 72 mg/kg; Not reported-mouse LD50: 200 mg/kg

flammability hazard characteristics

Thermal decomposition discharges toxic nitrogen oxides and bromide fumes

storage and transportation features

Warehouse ventilation and dry low temperature

fire extinguishing agent

Water, carbon dioxide, sand, foam, dry powder

Last Update:2024-04-10 22:29:15

25614-03-3 - Toxicity

An ergot alkaloid derivative that exhibits potent dopamine agonist properties, particularly at D2 dopamine receptors. Bromocriptine, like dopamine, inhibits prolactin release from the pituitary and so is used in endocrine disorders, such as hyperprolactinemia. It is also used in the treatment of Parkinson's disease. A large “first-pass” effect is seen with bromocriptine, and peak concentrations occur about 1.5-3 h after ingestion, with a half-life of about 3 h. Nausea, vomiting, and orthostatic hypotension are among the acute adverse effects. Long-term use has been associated with dyskinesias, constipation, psychoses, digital spasm, and erythromelalgia. The LD50 in rabbits exceeds 1 g/kg, p.o., and 12 mg/kg, I .v.

Last Update:2024-04-10 22:29:15
25614-03-3
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MedChemExpress (MCE)
Spot supply
Product Name: CB-154 free base Visit Supplier Webpage Request for quotation
CAS: 25614-03-3
Tel: 609-228-6898
Email: sales@medchemexpress.com
     tech@medchemexpress.com
Mobile: 609-228-6898
Shanghai Yuanye Bio-Technology Co., Ltd.
Product Name: Bromocriptine Visit Supplier Webpage Request for quotation
CAS: 25614-03-3
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409 Click to send a QQ message
View History
25614-03-3
2-甲氧基乙氧基氯硅烷
(3alpha,5beta,6beta,7alpha,12alpha)-3,6,7,12-tetrahydroxycholan-24-oic acid
4-(2-Pyrimidinyloxy)benzenecarbonitrile
顺-9-十六碳烯酸乙酯
Raw Materials for 25614-03-3
BROMOSUCCINIC ACID
ALPHA-ERGOCRYPTINE
N-Bromosuccinimide
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