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Pergolide mesylate salt

CAS No.
66104-23-2
Chemical Name:
Pergolide mesylate salt
Synonyms
MPE;PERGOLIDE MESYLATE;Pergolide methanesulfonate;Nopar;Permax;Celance;Veceral;Pergolin;ly127809;NSC 319773
CBNumber:
CB9455089
Molecular Formula:
C20H30N2O3S2
Molecular Weight:
410.59
MDL Number:
MFCD00153859
MOL File:
66104-23-2.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-08-04 11:17:55

Pergolide mesylate salt Properties

Melting point 252-254°C
alpha aD20 between -18.0° and -23.0° (c = 10 mg/ml in DMF)
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility ethanol: soluble2mg/mL
form solid
pka pKa (66% DMF) 7.8(at 25℃)
color white
optical activity [α]20/D 35°, c = 0.2 in pyridine(lit.)
InChIKey UWCVGPLTGZWHGS-PLBOZXOQNA-N
SMILES C12=C3C=CC=C1[C@@]1([H])C[C@H](CN(CCC)[C@]1([H])CC2=CN3)CSC.S(=O)(=O)(O)C |&1:6,9,15,r|
CAS DataBase Reference 66104-23-2(CAS DataBase Reference)
FDA UNII 55B9HQY616
UNSPSC Code 12352200
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H300
Precautionary statements  P301+P330+P331+P310
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  T+
Risk Statements  28
Safety Statements  28-36/37-45
RIDADR  UN 1544
WGK Germany  3
RTECS  KE6345000
HS Code  2939690000
Storage Class 6.1B - Non-combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
Hazard Classifications Acute Tox. 2 Oral

Pergolide mesylate salt price More Price(52)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0000010 Pergolide mesilate European Pharmacopoeia (EP) Reference Standard 66104-23-2 150 mg $241 2026-04-30 Buy
Sigma-Aldrich 1510845 Pergolide mesylate United States Pharmacopeia (USP) Reference Standard 66104-23-2 200mg $493 2026-04-30 Buy
Cayman Chemical 26085 Pergolide (mesylate) ≥95% 66104-23-2 5mg $54 2026-04-30 Buy
Cayman Chemical 26085 Pergolide (mesylate) ≥95% 66104-23-2 10mg $103 2026-04-30 Buy
Cayman Chemical 26085 Pergolide (mesylate) ≥95% 66104-23-2 25mg $244 2026-04-30 Buy
Product number Packaging Price Buy
Y0000010 150 mg $241 Buy
1510845 200mg $493 Buy
26085 5mg $54 Buy
26085 10mg $103 Buy
26085 25mg $244 Buy

Pergolide mesylate salt Chemical Properties, Uses, Production

Description

Pergolide mesylate is a potent, long-acting dopamine agonist useful in the treatment of Parkinson’s disease and hyperprolactinemia, Compared with lergotrile, pergolide mesylate has shown less toxicity and lower propensity for inducing psychosis.

Description

Pergolide is a potent dopamine D1 and D2 receptor agonist (Kis = 111 and 0.495 nM, respectively, for rat striatal receptors). It depresses dopaminergic firing in paralyzed rats (ED50 = <20 μg/kg), an effect that can be reversed by the dopamine D2-selective antagonist spiperone or the dopamine D1-selective antagonist SCH 23390 . Pergolide (0.025 and 0.05 mg/kg) increases the volume threshold for inducing bladder contraction in a cynomolgus monkey model of Parkinson''s disease induced by MPTP. It also reduces carrageenan-induced paw edema in adrenalectomized rats (ED50 = 0.4 mg/kg).

Chemical Properties

White to Off-White Solid

Originator

Lilly (USA)

Uses

A dopaminergic agonist that also decrease plasma prolactin concentrations. An antiparkinsonian agent

Uses

glucocorticoid, antiinflammatory

Uses

dopamine receptor agonist, anti-Parkinson's agent

Definition

ChEBI: A methanesulfonate salt obtained from pergolide by mixing eqimolar amount of pergolide and methanesulfonic acid. A dopamine D2 receptor agonist which also has D1 and D2 agonist properties, it i used in the management of Parkinson's disease, although it was withdrawn from the U.S. and Canadian markets in 2007 due to an increased risk of cardiac valve dysfunction.

Manufacturing Process

Dimethyl disulfide (73.6 ml, 0.79 mol) and tri-n-butylphosphine (79.6 ml, 0.32 mol) were added to a solution of 9,10-dihydrolysergol in (8.1 g, 0.032 mol) in the 150 ml of anhydrous DMF and were stirred at room temperature for 6 hours under a nitrogen atmosphere. Dimethyl disulfide of the reaction mixture was removed under vacuo. A solution of the residue in ethyl acetate was extracted with 3.7% HCl (aq.). The aqueous layer was basified with ammonium hydroxide to a pH of 10 and then extracted with ethyl acetate. Removal of ethyl acetate followed by a silica gel column purification eluting with 10% MeOH/CH2Cl2 gave5.5.g of D-6-methyl-8β(methylthiomethyl)ergoline (60%).
A solution of D-6-methyl-8β-(methylthiomethyl)ergoline (0.4 g, 0.0014 mol) and NaI (0.63 g, 0.0042 mol) in 10 ml of propionic anhydride was refluxed for 40 hours. The reaction mixture was guenched with a 10% Na2CO3 solution and extracted by ethyl acetate. The combined organic layers were washed with a saturated brine solution, dried with magnesium sulfate and concentrated to produce oil. The oil was purified by silica gel column, eluting with 10% MeOH/CH2Cl2 to give 0.33 g of D-1,6-dipropionyl-8β(methylthiomethyl)ergoline.
LiAlH4 (0.6 g, 0.0156 mol) was slowly added to a solution of D-1,6dipropionyl-8β-(methylthiomethyl)ergoline in the 20 ml anhydrous THF at 0°C under nitrogene atmosphere. The mixture was stirred at 0°C for 30 min and then at room temperature for 4 hours. The reaction was cooled to 0°C and 0.6 ml of water was slowly added. The mixture was stirred at 0°C for 10 min and 1.8 ml of 15% NaOH (aq.) and 2.5 ml of water were added respectively. The mixture was stirred for 30 min at room temperature and then filtered. Excess of the solvent was removed under reduced pressure to give 150 mg of 8β-((methylthio)methyl)-6-propyl-ergoline or pergolide (yield: 68%). Ergoline,8-((methylthio)methyl)-6-propyl-, monomethanesulfonate, (8β)- may be prepared by mixing of components in solution.

brand name

Permax (Valeant).

Therapeutic Function

Dopamine agonist

Biochem/physiol Actions

Dopaminergic agonist; suppresses pituitary secretion of prolactin; anti-Parkinsonian agent.

References

[1] M MIYAGI. Dopamine receptor affinities in vitro and stereotypic activities in vivo of cabergoline in rats.[J]. Biological & pharmaceutical bulletin, 1996, 19 9: 1210-1213. DOI: 10.1248/bpb.19.1210
[2] X X ZHANG  Y F W  G Z Jin. Agonistic actions of pergolide on firing activity of dopamine neurons in substantia nigra compacta area.[J]. Zhongguo yao li xue bao = Acta pharmacologica Sinica, 1995, 16 5: 423-427.
[3] N YOSHIMURA. Therapeutic effects of dopamine D1/D2 receptor agonists on detrusor hyperreflexia in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-lesioned parkinsonian cynomolgus monkeys.[J]. Journal of Pharmacology and Experimental Therapeutics, 1998, 286 1: 228-233.
[4] A M BENDELE. Anti-inflammatory activity of pergolide, a dopamine receptor agonist.[J]. Journal of Pharmacology and Experimental Therapeutics, 1991, 259 1: 169-175.

Pergolide mesylate salt Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 169)
Supplier Tel Email Country ProdList Advantage
Tianjin Keluo Pharmaceutical Technology Co. LTD 022-23869539 18920052327 281258989@qq.com China 65 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
ZHIWE CHEMTECH CO LTD 021-20221225 13917446399 zwchem@163.com China 525 61
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50
Spectrum Chemical Manufacturing Corp. 021-021-021-67601398-809-809-809 15221380277 marketing_china@spectrumchemical.com China 9643 60
BOC Sciences 1-631-485-4226; 16314854226 info@bocsci.com United States 9920 65
Shanghai Aladdin Bio-Chem Technology Co.,LTD 400-6206333 13167063860 anhua.mao@aladdin-e.com China 29985 65
MedChemexpress LLC 021-58955995 sales@medchemexpress.cn United States 4853 58
TargetMol Chemicals Inc. 021-021-33632979 15002134094 marketing@targetmol.com China 7993 58
Suzhou Pharmaceutical Technology co.,ltd 0510-88771160 18051901298 2013446823@qq.com China 53 61

View Latest Price from Pergolide mesylate salt manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Pergolide mesylate salt pictures 2026-08-03 Pergolide mesylate salt
66104-23-2
1kg 98% 1000kg Shaanxi Dideu New Materials Co. Ltd
Pergolide mesylate pictures 2026-07-15 Pergolide mesylate
66104-23-2
$47.00-117.00 99.70% 10g TargetMol Chemicals Inc.
Pergolide mesylate salt  pictures 2020-02-26 Pergolide mesylate salt
66104-23-2
100g 99%+ 10 tons Shaanxi Dideu Medichem Co. Ltd
8BETA-[(METHYLTHIO)METHYL]-6-PROPYLERGOLINE MESYLATE SALT 8-BETA-[(METHYLTHIO)METHYL]-6-PROPYLERGOLINE MONOMETHANE SULFONATE Pergolide mesylate EPIV Pergolidemetylsulfonate (8b)-8-[(Methylthio)methyl]-6-propylergoline Mesylate Celance Nopar Permax 8-alpha-Methylthiomethyl-6-pro 8β-[(methylthio)methyl]-6-propylergoline methanesulfonate salt Ergoline, 8-[(methylthio)methyl]-6-propyl-, (8b)-, monomethanesulfonate (9CI) NSC 319773 (8)-8-[(Methylthio)methyl]-6-propylergoline Mesylate Pergolide methanesulfonate salt, 8β-[(Methylthio)methyl]-6-propylergoline methanesulfonate salt Pergolin Veceral Pergolide methanesulfonate salt 8beta-[(Methylthio)methyl]-6-propylergoline methanesulfonate salt beta-((Methylthio)Methyl)-6-propylergolineMethanesulfonate Pergolide Mesylate, USP Pergolide Mesylate (200 mg) Ergoline, 8-[(methylthio)methyl]-6-propyl-, (8β)-, monomethanesulfonate (9CI) (8beta)-8-[(methylthio)methyl]-6-propyl-Ergoline monomethanesulfonate (9CI) 8-beta-((methylthio)methyl)-6-propylergolinemethanesulfonate 8-beta-((methylthio)methyl)-6-propyl-ergolinmethanesulfonate(1:1) ly127809 PERGOLIDE MESYLATE SALT Pergolide mesilate CRS Pergolide mesylate salt, 98%, an antiparkinsonian agent which functions as a dopaminergic agonist (6aR,9R,10aR)-9-[(Methylsulfanyl)methyl]-7-propyl- 4,6,6a,7,8,9,10,10a-octahydroindolo[4,3-fg]quinoline monomethanesulfonate Pergolide mesylate salt USP/EP/BP Pergolide Mesylate (LY127809) Veterinary Drugs Pergolide mesylate salt Pergolide Mesylate (1510845) Pergolide mesylate, 10 mM in DMSO (6aR,9R,10aR)-9-(Methylsulfanylmethyl)-7-propyl-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinoline MPE Pergolide methanesulfonate PERGOLIDE MESYLATE Ethyl 6-methoxy-α-oxo-1H-indole-3-acetate 66104-23-2 68104-23-2 C20H30N2O3S2 C21H18N3O2 C19H26N2SCH4O3S LOCOID API Intermediates & Fine Chemicals Neurochemicals Pharmaceuticals