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Buspirone hydrochloride

CAS No.
33386-08-2
Chemical Name:
Buspirone hydrochloride
Synonyms
BUSPIRONE HCL;Narol;bespar;axoren;travin;Ansial;censpar;lucelan;Ansiced;buspinol
CBNumber:
CB8367136
Molecular Formula:
C21H32ClN5O2
Molecular Weight:
421.96
MDL Number:
MFCD00078569
MOL File:
33386-08-2.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-27 17:00:41
Product description Number Pack Size Price
Buspirone for system suitability European Pharmacopoeia (EP) Reference Standard Y0000471 2 mg $254
Buspirone hydrochloride European Pharmacopoeia (EP) Reference Standard Y0000131 15 mg $164
Buspirone hydrochloride solution 1.0?mg/mL in methanol (as free base), ampule of 1?mL, certified reference material, Cerilliant? B-054 1mL $84.6
Buspirone hydrochloride United States Pharmacopeia (USP) Reference Standard 1078802 200mg $459
Buspirone hydrochloride European Pharmacopoeia (EP) Reference Standard Y0000131 5 mg $153
More product size

Buspirone hydrochloride Properties

Melting point 201.5-202.50C
Flash point 9℃
storage temp. 2-8°C
solubility Freely soluble in water and in methanol, practically insoluble in acetone.
form Solid
color White to off-white
Water Solubility Soluble in methanol (50 mg/ml), water (partly), DMSO (100 mM).
Major Application pharmaceutical
InChI InChI=1S/C21H31N5O2.ClH/c27-18-16-21(6-1-2-7-21)17-19(28)26(18)11-4-3-10-24-12-14-25(15-13-24)20-22-8-5-9-23-20;/h5,8-9H,1-4,6-7,10-17H2;1H
InChIKey RICLFGYGYQXUFH-UHFFFAOYSA-N
SMILES C12(CCCC1)CC(N(CCCCN1CCN(C3=NC=CC=N3)CC1)C(=O)C2)=O.Cl
CAS DataBase Reference 33386-08-2(CAS DataBase Reference)
FDA UNII 207LT9J9OC
NCI Drug Dictionary buspirone hydrochloride
UNSPSC Code 41116107
NACRES NA.77

Pharmacokinetic data

Protein binding 95%
Volume of distribution 2.69-7.91(L/kg)
Biological half-life 2-11 / 4-131

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H301
Precautionary statements  P264-P270-P301+P310-P405-P501
Hazard Codes  T,Xn,F
Risk Statements  25-36/37/38-20/21/22-39/23/24/25-23/24/25-11
Safety Statements  45-36-26-36/37-16
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS  CL9915000
HazardClass  6.1
HS Code  29335995
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Acute Tox. 3 Oral
Toxicity LD50 i.p. in rats: 136 mg/kg (Allen)
NFPA 704
0
2 0

Buspirone hydrochloride price More Price(60)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0000471 Buspirone for system suitability European Pharmacopoeia (EP) Reference Standard 33386-08-2 2 mg $254 2026-04-30 Buy
Sigma-Aldrich Y0000131 Buspirone hydrochloride European Pharmacopoeia (EP) Reference Standard 33386-08-2 15 mg $164 2026-04-30 Buy
Sigma-Aldrich B-054 Buspirone hydrochloride solution 1.0?mg/mL in methanol (as free base), ampule of 1?mL, certified reference material, Cerilliant? 33386-08-2 1mL $84.6 2026-04-30 Buy
Sigma-Aldrich 1078802 Buspirone hydrochloride United States Pharmacopeia (USP) Reference Standard 33386-08-2 200mg $459 2026-04-30 Buy
Sigma-Aldrich Y0000131 Buspirone hydrochloride European Pharmacopoeia (EP) Reference Standard 33386-08-2 5 mg $153 2025-07-31 Buy
Product number Packaging Price Buy
Y0000471 2 mg $254 Buy
Y0000131 15 mg $164 Buy
B-054 1mL $84.6 Buy
1078802 200mg $459 Buy
Y0000131 5 mg $153 Buy

Buspirone hydrochloride Chemical Properties,Uses,Production

Description

Buspirone hydrochloride is an anxiolytic agent indicated for the management of anxiety disorders with or without accompanying depression. In contrast to the benzodiazepines, buspirone does not interact with alcohol, and lacks sedative, anticonvulsant, and muscle relaxant effects, and abuse potential.

Chemical Properties

White Solid

Originator

Mead Johnson (USA)

Uses

Non-benzodiazepine anxiolitic; 5-hydroxytryptamine (5-HT1) receptor agonist.

Uses

Non-benzodiazepine anxiolytic; 5-hydroxytryptamine (5-HT1) receptor agonist.

Uses

anxiolitic;serotonin receptor agonist

Definition

ChEBI: A hydrochloride salt resulting from the reaction of equimolar amounts of buspirone and hydrogen chloride.

Manufacturing Process

There is the 3 methods for preparing of 8-azaspiro(4.5)decane-7,9-dione, 8- (4-(4-(2-pyrimidinyl)-1-piperazinyl)butyl) monohydrochloride (U.S. Patent 3,717,634). One of them is follows: a mixture of 0.1 mole of the substituted glutaric anhydride, 0.1 mole of l-(4-aminobutyl)-4-(2-pyrimidinyl)piperazine (U.S. Pat. 3,398151), and 300 ml of pyridine was refluxed until imide formation was completed. The degree of reaction was readily followed by taking an aliquot portion of the reaction mixture, removing the solvent, and obtaining the infrared absorption spectrum of the residue. When reaction is complete, the spectrum exhibited typical infrared imide bands at 1701 and 1710 cm-1 whereas if incomplete, the infrared spectrum contains amide and carboxyl absorption bands at 1680, 1760 and 3300 cm-1.
1-(3-Cyanopropyl)-4-(2-pyrimidinyl)-piperazine. A mixture of 1-(2- pyrimidinyl)piperazine (6.0 g, 0.04 mole), 4.6 g (0.044 mole) of 3- chloropropionitrile and sodium carbonate (4.24 g, 0.04 mole) in 50 ml of nbutanol was gently refluxed for 16 hours. The reaction mixture was concentrated in vacuo and the residual oil dissolved in about 100 ml of cyclohexane. On standing a white crystalline material separated which was crystallized from cyclohexane to provide 6.5 g (yield 70%) of the cyano intermediate, m.p. 56.6-58°C. A solution of 11.5 g (0.05 mole) of 1-(3- cyanopropyl)-4-(2-pyrimidinyl)piperazine in 150 ml of absolute ethanol was saturated with ammonia. W-6 Raney nickel catalyst was added and the mixture hydrogenated under 1200 p.s.i. When the hydrogenation was completed the mixture was filtered and the residual oil distilled under reduced pressure to provide 8.2 g (70% ) of 1-(4-aminobutyl)-4-(2- pyrimidinyl)piperazine, b.p. 143-146°C at 0.1 mm. (nD 26 = 1.5582).
The azospiroalkenedione 8-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]-8- azaspiro[4.5]decane-7,9-dione was purified as free base by stripping off the pyridine solvent and crystallizing the residue from a suitable solvent or by vacuum distillation thereof hydrochloric salt of it was prepared by treating of an ethanol solution of free base with equimolar amount of HCl.

brand name

Buspar (Bristol-Myers Squibb);BESPAR.

Therapeutic Function

Anxiolytic

General Description

Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards

Biological Activity

Classic 5-HT 1A partial agonist with relatively high affinity (K i = 9.3 - 29.5 nM). A clinically effective anxiolytic.

Biochem/physiol Actions

5-HT1A serotonin receptor agonist; anxiolytic.

Clinical Use

Anxiolytic

Veterinary Drugs and Treatments

Buspirone may be effective in treating certain behavior disorders in dogs and cats, principally those that are fear/phobia related and especially those associated with social interactions. Buspirone may also be useful for urine spraying or treatment of motion sickness in cats.

Drug interactions

Potentially hazardous interactions with other drugs
Antibacterials: concentration increased by erythromycin - reduce dose; concentration reduced by rifampicin.
Antidepressants: avoid with tranylcypromine; risk of severe hypertension with MAOIs - avoid.
Antifungals: concentration increased by itraconazole - reduce dose.
Antipsychotics: enhanced sedative effects; haloperidol concentration increased.
Antivirals: concentration increased by ritonavir, increased risk of toxicity.
Calcium-channel blockers: concentration increased by diltiazem and verapamil - reduce dose.
Grapefruit juice: concentration increased by grapefruit juice - reduce dose.
Methylthioninium: possible risk of CNS toxicity - avoid if possible.

Metabolism

Systemic bioavailability of buspirone is low because of extensive first-pass metabolism. Metabolism in the liver is extensive via the cytochrome P450 isoenzyme CYP3A4; hydroxylation yields several inactive metabolites and oxidative dealkylation produces 1-(2-pyrimidinyl)- piperazine, which is reported to be about 25% as potent as the parent drug in one model of anxiolytic activity. Buspirone is excreted mainly as metabolites in the urine, and also the faeces.

storage

+4°C (desiccate)

Global( 335)Suppliers
Supplier Tel Email Country ProdList Advantage
Shandong Risen-Sun Pharmaceutical Co. LTD
+86-13958575904 risensun@jewim.com.cn China 86 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21533 55
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29766 58
CONIER CHEM AND PHARMA LIMITED
sales@conier.com China 49906 58
TargetMol Chemicals Inc.
+1-781-999-5354; +1-00000000000 marketing@targetmol.com United States 32431 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +86-189 4982 3763 sales@tnjchem.com China 34526 58
Dideu Industries Group Limited
+8617392712697 1022@dideu.com China 29094 58
AFINE CHEMICALS LIMITED
+86-571-85134551 +86-18958018566 info@afinechem.com China 15050 58
Wuhan Fortuna Chemical Co., Ltd
+86-27-59207850 info@fortunachem.com China 5986 58
BOC Sciences
16314854226; +8616314854226 inquiry@bocsci.com United States 19852 58

View Lastest Price from Buspirone hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Buspirone hydrochloride pictures 2026-08-29 Buspirone hydrochloride
33386-08-2
1KG 98.5%min 100KGS WUHAN FORTUNA CHEMICAL CO., LTD
Buspirone hydrochloride pictures 2026-08-25 Buspirone hydrochloride
33386-08-2
$80.00-800.00 10kg 0.99 20tons Zibo Hangyu Biotechnology Development Co., Ltd
Buspirone hydrochloride pictures 2026-08-21 Buspirone hydrochloride
33386-08-2
$50.00 99.96% 10g TargetMol Chemicals Inc.

Buspirone hydrochloride Spectrum

8-[4-[4-(2-pyrimidinyl)-1-piperazin-1-iumyl]butyl]-8-azaspiro[4.5]decane-7,9-dione 8-[4-[4-(2-PYRIMIDINYL)-1-PIPERAZINYL]BUTYL]-8-AZASPIRO[4,5]DECANE-7,9-DIONE HYDROCHLORIDE 1-cyclopentanediacetimide,n-(4-(4-(2-pyrimidinyl)-1-piperazinyl)butyl)-h 8-(4-(4-(2-pyrimidinyl)-1-piperazinyl)butyl)-8-azaspiro(4.5)decane-9-dione axoren bespar buspinol buspironechloridate BUSPIRONE HYDROCHLORIDE N-[4-(4-[2-PYRIMIDINYL]-1-PIPERAZINYL)BUTYL]-8-AZASPIRO[4,5]DECANE-7,9-DIONE HYDROCHLORIDE censpar lucelan mj9022-1 travin 8-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]-8-azaspiro[4.5]decane-7,9-dione monohydrochloride 8-(4-(4-(2-Pyrimidinyl)-1-piperizinyl)butyl)-8-azaspiro(4,5)decane-7,9-dione hydrochloride 3-[4-[4-(2-Pyrimidinyl)piperazino]butyl]-3-azaspiro[5.4]decane-2,4-dione·hydrochloride Ansial Ansiced Narol 8-Azaspiro4.5decane-7,9-dione, 8-4-4-(2-pyrimidinyl)-1-piperazinylbutyl-, monohydrochloride BUSPIRONEHYDROCHLORIDE,USP 5,6-DICHLORO-2-(ISOPROPYLAMINO)-1-(BETA-L-RIBOFURANOSYL)-LH-BENZIMIDAZOLE Buspirone Hydrochlorid N-[4-[4-(2-Pyrimidinyl)-1-piperazinyl]butyl]-1,1-cyclopentanediacetimide hydrochloride 1-Cyclopentanediacetimide,N-(4-(4-( 8-[4-[4-(2-Pyrimidinyl)-1-pipirazinyl]butyl]-8-azaspiro[4,5]decane-7,9-dionehydrochloride Buspirone hydrochloride,N-[4-[4-(2-Pyrimidinyl)-1-piperazinyl]butyl]-8-azaspiro[4.5]decane-7,9-dione hydrochloride Buspirone Hydrochloride (200 mg) 8-(4-(4-(Pyrimidin-2-yl)piperazin-1-yl)butyl)-8-azaspiro[4.5]decane-7,9-dione hydrochloride 8-Azaspiro[4.5]decane-7,9-dione,8-[4-[4-(2-pyriMidinyl)-1-piperazinyl]butyl]-, hydrochloride (1:1) Buspirone hydrochloride solution Buspirone hydrochloride CRS Buspirone hydrochloride USP/EP/BP Birone hydrochloride Buspirone HCl (MJ90221) Buspirone for system suitability(Secondary Standards traceble to EP) Buspirone HydrochlorideQ: What is Buspirone Hydrochloride Q: What is the CAS Number of Buspirone Hydrochloride Q: What is the storage condition of Buspirone Hydrochloride Q: What are the applications of Buspirone Hydrochloride Buspirone Hydrochloride (1078802) Buspirone HCl (MJ90221) HCl 8-(4-(4-(pyrimidin-2-yl)piperazin-1-yl)butyl)-8-azaspiro[4.5]decane-7,9-dione, hydrochloride (1:1) Buspirone Hydrochloride 8-[4-[4-(Pyrimidin-2-yl)piperazin-1-yl]butyl]-8-azaspiro[4.5]- decane-7,9-dione hydrochloride Buspirone hydrochloride in Methanol Buspirone hydrochloride, 5-HT1A agonist Buspirone hydrochloride, 10 mM in DMSO Buspirone HCl - Bio-X ? Buspirone (hydrochloride) (CRM) Buspirone.HCl, 1mg/ml in Methanol (as free base) Buspirone Hydrochloride 1.0 mg/ml in Methanol (as free base) N-[4-[4-(2-Pyrimidinyl)-1-piperazinyl]butyl]-8-azaspiro[4.5]decan-7,9-dione hydrochloride BUSPIRONE HCL 33386-08-2 C21H32ClN5O2 C21H31N5O2HCl C21H32N5O2 C21H31N5O2xHCl 42196 Inhibitors