ChemicalBook > CAS DataBase List > Bromocriptine

Bromocriptine

Product Name
Bromocriptine
CAS No.
25614-03-3
Chemical Name
Bromocriptine
Synonyms
Parlodel;bromoergocryptine;BROMOCRITINE;bromocryptine;2-bromo-ergocryptin;Kripton;SAN 15-754;bromocriptin;,6’,18-trione;BROMOCRIPTINE
CBNumber
CB6136426
Molecular Formula
C32H40BrN5O5
Formula Weight
654.59
MOL File
25614-03-3.mol
More
Less

Bromocriptine Property

Melting point:
215-218° (dec)
alpha 
D20 -195° (c = 1 in methylene chloride)
Boiling point:
891.3±65.0 °C(Predicted)
Density 
1.2734 (rough estimate)
refractive index 
1.6400 (estimate)
pka
pKa 4.90±0.05(80% MCS t = RT) (Uncertain)
Water Solubility 
2.07mg/L(temperature not stated)
CAS DataBase Reference
25614-03-3(CAS DataBase Reference)
More
Less

Safety

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.
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H361Suspected of damaging fertility or the unborn child

H362May cause harm to breast-fed children

Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P263Avoid contact during pregnancy/while nursing.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P281Use personal protective equipment as required.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P308+P313IF exposed or concerned: Get medical advice/attention.

P330Rinse mouth.

P405Store locked up.

P501Dispose of contents/container to..…

More
Less

Bromocriptine Chemical Properties,Usage,Production

Chemical Properties

Crystals.

Originator

Parlodel,Sandoz,UK,1975

Uses

Enzyme inhibitor (prolactin).

Uses

Bromocriptine, a dopaminomimetic that is a dopamine D2 receptor agonist, possesses expressed antiparkinsonian activity. It is used for treating all phases of idiopathic and postencephalic Parkinsonism.

Definition

An semisynthetic ergotamine alkaloid derivative and powerful dopamine D2 agonist. It inhibits prolactin secretion and release from the pituitary and retards tumor growth.

Manufacturing Process

A solution of 3.4 grams of N-bromosuccinimide in 60 cc of absolute dioxane is added drop wise in the dark, during the course of 5 minutes, to a stirred solution, heated to 60°C, of 9.2 grams of ergocryptine in 180 cc of absolute dioxane. The reaction mixture is stirred at this temperature for 70 minutes and is concentrated to a syrup-like consistency in a rotary evaporator at a bath temperature of 50°C. The reaction mixture is subsequently diluted with 300 cc of methylene chloride, is covered with a layer of about 200 cc of a 2 N sodium carbonate solution in a separating funnel and is shaken thoroughly. The aqueous phase is extracted thrice with 100 cc amounts of methylene chloride. The combined organic phases are washed once with 50 cc of water, are dried over sodium sulfate and the solvent is removed under a vacuum.
The resulting brown foam is chromatographed on a 50-fold quantity of aluminum oxide of activity II-III with 0.2% ethanol in methylene chloride as eluant, whereby the compound indicated in the heading is eluted immediately after a secondary fraction which migrates somewhat more rapidly than the fractions containing the heading compound. The last fractions to leave the aluminum oxide contain varying amounts of starting material together with the heading compound, and may be subjected directly, as mixed fractions, to an afterbromination in accordance with the method described above. The fractions containing the pure heading compound are combined and crystallized from methyl ethyl ketonehopropy1 ether. Melting point 215°-218°C (decomp.), [α]D 20-195° (c = 1 in methylene chloride).

brand name

Parlodel (Novartis);Bromed;Lactismine;Parilac;Umprel.

Therapeutic Function

Prolactin inhibitor

World Health Organization (WHO)

Bromocriptine, a semisynthetic ergot alkaloid derivative and prolactin inhibitor was introduced into medicine in 1976. It is used in the prevention of lactation, but because of the risk of rebound effect and since only 10% of women benefit therapeutically from such intervention, the United States Food and Drug Administration has requested manufacturers to no longer indicate preparations containing bromocriptine for this purpose. The World Health Organization is not aware of similar action having been taken elsewhere.

Hazard

Poison; teratogen; developmental abnor- malities of the respiratory system,musculoskeletal system, rogenital system, craniofacial area, and body wall; teratogen; mutagen; questionable car- cinogen; tumorigen; causes nausea, vomiting, orthostatic hypotension; constipation, dyskinesias, psychoses, digital spasm, erythromelalgia.

Mechanism of action

Bromocriptine is absorbed after oral administration, but approximately 90% of a dose undergoes extensive first-pass hepatic metabolism, with the remainder hydrolyzed in the liver to inactive metabolites that are eliminated mostly in the bile. The half-life is relatively short (~3 hours).

Clinical Use

Bromocriptine is an ergot peptide derivative that is a partial agonist at D1-type and a full agonist at D2-type postsynaptic dopamine receptors, usually given in combination with levodopa therapy. It was the first direct dopamine receptor agonist used in treatment of Parkinson's disease after its development as an inhibitor of prolactin release (via activation of anterior pituitary D2 receptors). At low doses (typically 1–5 mg/day), bromocriptine is an effective prolactin inhibitor, and at higher doses (typically 10–20 mg/day), the antiparkinsonism and mood-elevating effects of bromocriptine become apparent.

Side effects

Bromocriptine has a number of undesirable side effects, even causing mental disturbances in long-term use.

Synthesis

Bromocriptine, 2-bromoergocriptine (10.1.13), is a semisynthetic derivative of a natural ergot alkaloid, ergocriptin (a derivative of lysergic acid), which is synthesized by bromination of ergocriptin using N-bromosuccinimide [18,19].

Drug interactions

Potentially hazardous interactions with other drugs
Increased risk of toxicity with bromocriptine and isometheptene.

Metabolism

Bromocriptine is extensively metabolised. It undergoes extensive first-pass biotransformation in the liver, reflected by complex metabolite profiles and by almost complete absence of parent drug in urine and faeces. In plasma the elimination half life is 3-4 hours for the parent drug and 50 hours for the inactive metabolites.The parent drug and its metabolites are also completely excreted via the liver with only 6% being eliminated via the kidney.

Bromocriptine Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Bromocriptine Suppliers

NCE Biomedical Co.,Ltd.
Tel
4000-027-021 |24 +86-13986109188 | +86-15623472865 | +81-08033611988
Fax
+86-27-87599188
Country
China
ProdList
1494
Advantage
55
ShangHai Caerulum Pharma Discovery Co., Ltd.
Tel
18149758185
Email
sales-cpd@caerulumpharma.com
Country
China
ProdList
3421
Advantage
58
ChemStrong Scientific Co.,Ltd
Tel
0755-0755-66853366 13670046396
Fax
0755-28363542
Email
sales@chem-strong.com
Country
China
ProdList
17982
Advantage
56
Chizhou Kailong Import and Export Trade Co., Ltd.
Tel
Fax
-
Email
xg01_gj@163.com
Country
China
ProdList
9503
Advantage
50
Shanghai Chaolan Chemical Technology Center
Tel
QQ:65489617 15618227136
Fax
21-5161 9052
Email
info@SuperLan-chem.com
Country
China
ProdList
9445
Advantage
58
Shanghai Witofly Chemical Co. ,Ltd.
Tel
021-021-50630626 18964684208
Email
sales@witofly.com
Country
China
ProdList
1150
Advantage
55
Shanghai Zhibang Biological Medicine Co., LTD
Tel
021-54285032 18116461626
Fax
021-54285032
Email
25493162@qq.com
Country
China
ProdList
133
Advantage
58
Shaanxi Jiandu Pharmaceutical Chemical Co. Ltd.
Tel
029-87576359 17691182729
Fax
029-88380327
Email
1018@dideu.com
Country
China
ProdList
1982
Advantage
58
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 13028896684
Email
sales@rrkchem.com
Country
China
ProdList
55827
Advantage
58
Hebei Yanxi Chemical Co., Ltd.
Tel
+8617531190177
Email
peter@yan-xi.com
Country
China
ProdList
5993
Advantage
58
Xi'an MC Biotech, Co., Ltd.
Tel
029-89275612 +8618991951683
Fax
8618991951683
Email
mcbio_sales@163.com
Country
China
ProdList
2255
Advantage
58
Hangzhou Huarong Pharm Co., Ltd.
Tel
571-86758373 +8613588754946
Fax
0086-571-81131109
Email
sales@huarongpharm.com
Country
CHINA
ProdList
3149
Advantage
58
Dideu Industries Group Limited
Tel
+86-29-89586680 +86-15129568250
Email
1026@dideu.com
Country
China
ProdList
28965
Advantage
58
Dayang Chem (Hangzhou) Co.,Ltd.
Tel
571-88938639 +8617705817739
Fax
+86-571-88938652,+86-571- 88492614
Email
info@dycnchem.com
Country
CHINA
ProdList
52867
Advantage
58
HUNAN CHEMFISH SCIENTIFIC CO.,LTD
Tel
+86-0731-85567275 13021512891
Fax
QQ:3554193828
Email
sales02@chemfish.com
Country
China
ProdList
6583
Advantage
58
Chemwill Asia Co.,Ltd.
Tel
86-21-51086038
Fax
86-21-51861608
Email
chemwill_asia@126.com
Country
CHINA
ProdList
23931
Advantage
58
Hubei Moco Chemical Co., Ltd.
Tel
18627756402
Fax
QQ:3001051413
Email
3001051413@qq.com
Country
China
ProdList
10009
Advantage
58
Shanghai Longyu Biotechnology Co., Ltd.
Tel
+8615821988213
Fax
+86 15821988213
Email
info@longyupharma.com
Country
China
ProdList
2531
Advantage
58
Chongqing Chemdad Co., Ltd
Tel
+86-023-61398051 +8613650506873
Email
sales@chemdad.com
Country
China
ProdList
39916
Advantage
58
Shenzhen Hengfeng Wanda Pharmaceutical Technology Co., Ltd
Tel
755-22677922-801 18126518403
Fax
518109
Email
2851922760@qq.com
Country
China
ProdList
5043
Advantage
58
Wuhan Wiseman Bioengineering Co.,Ltd
Tel
027-59506022 13419526507
Fax
027-59506022
Email
13419526507@163.com
Country
China
ProdList
2935
Advantage
58
Energy Chemical
Tel
021-58432009 400-005-6266
Fax
021-58436166
Email
marketing@energy-chemical.com
Country
China
ProdList
44941
Advantage
58
Changzhou Xianglong Pharmaceutical Technology Co., LTD
Tel
18661161657
Email
yaoxiangqiu2021@163.com
Country
China
ProdList
10066
Advantage
58
Molcoo Chemicals Inc.
Tel
18274848843
Email
3001006472@qq.com
Country
China
ProdList
8626
Advantage
58
Wuhan Beileye Biomedical Technology Co., Ltd.
Tel
18086118078
Email
2696158611@qq.com
Country
China
ProdList
4280
Advantage
58
Cato Research Chemicals Inc.
Tel
020-81960175-677 18933936954
Email
tianwen.zhan@cato-chem.com
Country
China
ProdList
7713
Advantage
58
Cdreamlab (Hubei) Technology Co., LTD
Tel
0717-6300888 18062399888
Email
service@cdreamlab.com
Country
China
ProdList
315
Advantage
58
Shaanxi kelkai Pharmaceutical Technology Co., Ltd
Tel
029-2148545164 17392779578
Email
2148545164@qq.com
Country
China
ProdList
6807
Advantage
58
Hangzhou Bingochem Co., Ltd.
Tel
0571-87632989
Email
sales@bingochem.com
Country
China
ProdList
21673
Advantage
58
Nantong Hanfang Biotechnology Co. , Ltd.
Tel
3674309880
Email
hanfangpharma@126.com
Country
China
ProdList
30968
Advantage
58
career henan chemical co
Tel
+86-0371-86658258
Email
sales@coreychem.com
Country
China
ProdList
29914
Advantage
58
hebei hongtan Biotechnology Co., Ltd
Tel
+86-86-1913198-3935 +8617331935328
Email
sales03@chemcn.cn
Country
China
ProdList
951
Advantage
58
Wuhan Han Sheng New Material Technology Co.,Ltd
Tel
+8617798174412
Email
admin01@hsnm.com.cn
Country
China
ProdList
2118
Advantage
58
GIHI CHEMICALS CO.,LIMITED
Tel
+8618058761490
Email
info@gihichemicals.com
Country
China
ProdList
50000
Advantage
58
PT CHEM GROUP LIMITED
Tel
+86-85511178 +86-85511178
Email
peter68@ptchemgroup.com
Country
China
ProdList
35453
Advantage
58
LEAP CHEM CO., LTD.
Tel
+86-852-30606658
Email
market18@leapchem.com
Country
China
ProdList
24738
Advantage
58
Shanghai Hao Zhun Biological Technology Co., Ltd.
Tel
--
Fax
--
Email
info@zzsrm.com
Country
CHINA
ProdList
6846
Advantage
58
Shanghai Hao Biological Technology Co., Ltd.
Tel
--
Fax
--
Email
shxiyuanbio@163.com
Country
CHINA
ProdList
6921
Advantage
58
More
Less

View Lastest Price from Bromocriptine manufacturers

hebei hongtan Biotechnology Co., Ltd
Product
Bromocriptine 25614-03-3
Price
US $30.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
2000kg
Release date
2024-03-26
Hebei Yanxi Chemical Co., Ltd.
Product
bromocriptine 25614-03-3
Price
US $40.00-40.00/kg
Min. Order
1kg
Purity
0.99
Supply Ability
10 tons
Release date
2023-09-27
Dideu Industries Group Limited
Product
Bromocriptine 25614-03-3
Price
US $1.10/g
Min. Order
1g
Purity
99.9%
Supply Ability
100 Tons min
Release date
2021-07-27

25614-03-3, BromocriptineRelated Search:


  • (5’-alpha)-ropyl)
  • ,6’,18-trione
  • 2-bromo-12’-hydroxy-2’-(1-methylethyl)-5’-alpha-(2-methylpropyl)ergotamin-3’
  • 2-bromo-alpha-ergocryptine
  • 2-bromo-alpha-ergokryptin
  • 2-bromo-alpha-ergokryptine
  • 2-bromo-ergocryptin
  • 2-bromoergocryptine
  • alpha-bromoergocriptine
  • bromergocryptine
  • bromocriptin
  • bromocryptine
  • bromoergocriptine
  • bromoergocryptine
  • ergotaman-3’,6’,18-trione,2-bromo-12’-hydroxy-2’-(1-methylethyl)-5’-(2-methylp
  • (5'alpha)-2-bromo-12'-hydroxy-2'-(1-methylethyl)-5'-(2-methylpropyl)ergotaman-3',6',18-trione
  • Kripton
  • Parlodel
  • BROMOCRIPTINE
  • Bromoergocryptine mesylate
  • BROMOCRITINE
  • 2-Bromo-α-ergokryptine
  • bromocripitine
  • Ergocryptine, 2-bromo- (8CI)
  • 2-Bromo-α-ergokryptin
  • ErgotaMan-3',6',18-trione,2-broMo-12'-hydroxy-2'-(1-Methylethyl)-5'-(2-Methylpropyl)-, (5'a)-
  • Bromocriptine\n\nDiscontinued, B682600
  • (5'a)-2-Bromo-12'-hydroxy-2'-(1-methylethyl)-5'-(2-methylpropyl)-ergotaman-3',6',18-trione
  • Ergotaman-3',6',18-trione, 2-bromo-12'-hydroxy-2'-(1-methylethyl)-5'-(2-methylpropyl)-, (5'α)-
  • SAN 15-754
  • Sandoz 15-754
  • Bromocriptine USP/EP/BP
  • BromocriptineQ: What is Bromocriptine Q: What is the CAS Number of Bromocriptine Q: What is the storage condition of Bromocriptine Q: What are the applications of Bromocriptine
  • 25614-03-3
  • 25614-03-2
  • C32H40BrN5O5
  • Organics