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Quetiapine fumarate

CAS No.
111974-72-2
Chemical Name:
Quetiapine fumarate
Synonyms
SEROQUEL;QUETIAPINE HEMIFUMARATE;Quetiapine heMifuMarate salt;ICI-204636;Quetine fumarate;QuetiapineFamarate;QUETIAPINE FUMARATE;Quitiapine Fumarate;Quetinapine Fumarate;Quintiapine fumarate
CBNumber:
CB9270451
Molecular Formula:
C25H29N3O6S
Molecular Weight:
499.58
MDL Number:
MFCD03423782
MOL File:
111974-72-2.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-16 07:06:08

Quetiapine fumarate Properties

Melting point 174-176°C
Flash point 9℃
storage temp. 2-8°C
solubility DMSO: >10mg/mL
form powder
color white to off-white
Merck 14,8039
BCS Class 2
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
InChIKey VRHJBWUIWQOFLF-WLHGVMLRSA-N
SMILES C(/C(=O)O)=C\C(=O)O.C(N1CCN(C2=NC3C=CC=CC=3SC3=CC=CC=C23)CC1)COCCO
CAS DataBase Reference 111974-72-2(CAS DataBase Reference)
FDA UNII 2S3PL1B6UJ
UNSPSC Code 41116107
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Environment (GHS09)
GHS07,GHS09
Signal word  Warning
Hazard statements  H302-H400
Precautionary statements  P273-P301+P312+P330
Hazard Codes  Xn,N,T,F
Risk Statements  22-50/53-52/53-39/23/24/25-23/24/25-11
Safety Statements  60-61-45-36/37-16
RIDADR  UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany  3
RTECS  KK3605000
HS Code  29349990
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Aquatic Acute 1
NFPA 704
0
3 0

Quetiapine fumarate price More Price(83)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0001657 Quetiapine fumarate European Pharmacopoeia (EP) Reference Standard 111974-72-2 50 mg $167 2026-04-30 Buy
Sigma-Aldrich Y0001419 Quetiapine for system suitability European Pharmacopoeia (EP) Reference Standard 111974-72-2 2 mg $167 2026-04-30 Buy
Sigma-Aldrich Q-001 Quetiapine fumarate solution 1.0?mg/mL in methanol (as free base), ampule of 1?mL, certified reference material, Cerilliant? 111974-72-2 1mL $118 2026-04-30 Buy
Sigma-Aldrich PHR1856 Quetiapine fumarate Pharmaceutical Secondary Standard; Certified Reference Material 111974-72-2 1g $248 2026-04-30 Buy
TCI Chemical Q0092 Quetiapine Hemifumarate >98.0%(HPLC)(T) 111974-72-2 5g $196 2026-04-30 Buy
Product number Packaging Price Buy
Y0001657 50 mg $167 Buy
Y0001419 2 mg $167 Buy
Q-001 1mL $118 Buy
PHR1856 1g $248 Buy
Q0092 5g $196 Buy

Quetiapine fumarate Chemical Properties, Uses, Production

Antipsychotics

Quetiapine fumarate is an antipsychotic, successfully developed by the AstraZeneca United States, it interacts with a variety of neurotransmitter receptors, in the brain, it displays high degree affinity for serotonin (5-HT2) receptor, and it is greater than dopamine D1 and D2 dopamine receptor affinity in the brain. Quetiapine also has high affinity for histamine H1 receptor and adrenergic α1 receptors, and low affinity for α2 receptors, but it basically displays no affinity for cholinergic muscarinic receptors or benzodiazepine receptors . It shows positive results in antipsychotic activity assays such as conditioned avoidance reflex . In clinical, it is mainly used in treatment for adults with severe depression, acute manic episodes of bipolar disorder and schizophrenia of different types . It is not only effective for the positive symptoms of schizophrenia, but also having a certain effect for negative symptoms . It can also alleviate affective symptoms associated with schizophrenia, such as depression, anxiety symptoms and cognitive deficits.
The above information is edited by the chemicalbook of Tian Ye.

Chemical properties

White crystalline powder.

Uses

A non-classical antipsychotics.

Description

Quetiapine hemifumarate (111974-72-2) is an atypical antipsychotic agent. Antagonist at serotonin (5-HT2) and dopamine (D2) receptors, IC50s=148 and 329 nM respectively.2 Reverses depressive-like behavior and reduces DNA methyltransferase activity induced by maternal deprivation in a rat model.3 Efficacious as a monotherapy in the treatment of posttraumatic stress disorder.4

Chemical Properties

White Crystalline Solid

Uses

Used as an antipsychotic. Benzothiazepine with mixed serotonin and dopamine receptor antagonistic properties

Uses

antihypertensive adrenergic receptor blocking agent with selective alpha1- and nonselective beta-adrenergic receptor blocking actions in a single substance.

Uses

Quetiapine hemifumarate salt has been used as an antagonist for β-arrestin 2 mutant T205M recruitment.

brand name

Seroquel (AstraZeneca).

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

Hazard

Human systemic effects.

Biochem/physiol Actions

Quetiapine hemifumarate is an atypical antipsychotic, a combined serotonin (5HT2) and dopamine (D2) receptor antagonist.

Synthesis

11-(1-PIPERAZINYL)-DIBENZO[B,F][1,4]THIAZEPIN HYDROCHLORIDE

753475-15-9

2-(2-Chloroethoxy)ethanol

628-89-7

Quetiapine fumarate

111974-72-2

General procedure for the synthesis of 2-(2-(4-(dibenzo[b,f][1,4]thiazepin-11-yl)piperazin-1-yl)ethoxy)ethan-1-ol hemifumarate from 11-(piperazin-1-yl)dibenzo[b,f][1,4]thiazepin-1-yl)ethoxy)ethan-1-ol: Reagents: 16.5 g (44 mmol) of 11-(piperazin-1-yl)dibenzo[b,f][1,4]thiazepine hydrochloride, 7.2 g (58 mmol) of 2-(2-chloroethoxy)ethanol, 28.5 g (270 mmol) of Na2CO3, 270 mg (0.18 mmol) of NaI, 3 g of TBAB, 82.5 mL of toluene. Steps: 1. add the above reagents to a round-bottomed flask equipped with a magnetic stirrer and a condenser with a calcium chloride drying tube. 2. Place the flask in an oil bath at 105°C and heat under mild reflux conditions. 3. after 24 hours, a Dean-Stark water separator is connected and the azeotropic mixture of water and toluene is distilled. 4. The residue in the flask was filtered and the precipitate (inorganic salt) was washed with a small amount of toluene on a Brinell funnel. 5. Combine the washings with the filtrate and discard the precipitate. 6. 2.6 g (22 mmol) of fumaric acid is added to the filtrate and the mixture is heated to boiling in a heating bath. 7. Remove the flask from the heating bath and continue stirring to precipitate quetiapine hemifumarate crystals. 8. The flask was cooled in an ice bath and the crystalline product was collected by filtration. 9. The resulting solid was recrystallized from 150 ml of ethanol. Yield: 14.0 g, 72% yield.

in vitro

quetiapine has shown affinity for various neurotransmitter receptorsincluding dopamine, serotonin, histamine, and adrenergicreceptors, quetiapine exihibited binding characteristics at the dopamine-2receptorsimilar to those of clozapine [1].

in vivo

in animal models, quetiapine exihibited a preclinical profile suggestive of antipsychotic activity with a reduced tendency to cause extrapyramidal symptoms (eps) and sustained prolactin elevation. quetiapine altered neurotensin neurotransmission and c-fos expression in limbic but not motor brain regions.in humans, quetiapine exhibited linear pharmacokinetics with a mean terminal half-life of 7 hours.the optimal dosing range for quetiapine was 150 to 750 mg/day, and recent results suggested that once-daily dosing might be suitable for some patients [1].quetiapine prevented schizophrenia and depression in hippocampal cell proliferation and bdnf expression caused by chronic restraint stress (crs) in rats in a dose-dependent manner. quetiapine (5 mg/kg) in combination with venlafaxine (2.5 mg/kg) increaseed hippocampal cell proliferation and prevented bdnf decrease in stressed rats, while each of the drugs exerted mild or no effects [2].in rats subjected to chronic-restraint stress, chronic administration of quetiapine attenuated the decrease in levels of brain-derived neurotrophic factor (bdnf) in the hippocampi. the stress-induced suppression of hippocampal neurogenesis was reversed after post-stress administration of quetiapine (10 mg/kg) for 7 or 21 days, evidenced in the numbers of pcreb-positive and brdu-labeled cells that were comparable to those in non-stressed rats but higher than those in the vehicle-treated rats [3].

target

Androgen Receptor | Estrogen receptor | Progestogen receptor

storage

+4°C

References

[1] BART A ELLENBROEK PH.D  Alexander R C Ph D  Luuk J Lubbers. Activity of “Seroquel” (ICI 204,636) in Animal Models for Atypical Properties of Antipsychotics: A Comparison with Clozapine[J]. Neuropsychopharmacology, 1996, 15 4: 406-416. DOI:10.1016/0893-133x(96)00001-2
[2] C F SALLER  A I S. Seroquel: biochemical profile of a potential atypical antipsychotic.[J]. Psychopharmacology, 1993, 112 2-3: 285-292. DOI:10.1007/bf02244923
[3] ZULEIDE M. IGNÁCIO . Quetiapine treatment reverses depressive-like behavior and reduces DNA methyltransferase activity induced by maternal deprivation[J]. Behavioural Brain Research, 2017, 320: Pages 225-232. DOI:10.1016/j.bbr.2016.11.044
[4] GERARDO VILLARREAL. Efficacy of Quetiapine Monotherapy in Posttraumatic Stress Disorder: A Randomized, Placebo-Controlled Trial.[J]. American Journal of Psychiatry, 2016, 173 12: 1205-1212. DOI:10.1176/appi.ajp.2016.15070967

110-17-8
111974-69-7
111974-72-2
Synthesis of Quetiapine fumarate from Fumaric acid and Quetiapine
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Quetiapine fumarate pictures 2026-09-17 Quetiapine fumarate
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Quetiapine fumarate Spectrum

QUETIAPINE HEMIFUMERATE Quetiapine fuMarate USP Quetiapine Fumarate Tablets Quetiapine (hemifumarate) (CRM) 2-[2-(4-Dibenzo [b,f] [1,4]thiazepin-11-yl-1-piperazinyl)ethoxy]-ethanol fumarate (2:1) (salt) Quetiapine hemifumarate salt, 98%, an inhibitor of D2DR and SR-2A 2-[2-(4-dibenzo[b,f][1,4]thiazepin-11-yl-1-piperazinyl)ethoxy]-ethanol,(2E)-2-butenedioate (2:1) Quetiapine fumarate solution Quetiapine for system suitability QuetiapineFamarate bis(2-[2-(4-{2-thia-9-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3,5,7,9,11,13-heptaen-10-yl}piperazin-1-yl)ethoxy]ethan-1-ol) bis(2-[2-(4-{2-thia-9-azatricyclo[9.4.0.0,3,8]pentadeca-1(15),3,5,7,9,11,13-heptaen-10-yl}piperazin-1-yl)ethoxy]ethan-1-ol), but-2-enedioic acid Ethanol, 2-[2-(4-dibenzo[b,f][1,4]thiazepin-11-yl-1-piperazinyl)ethoxy]-, (2E)-2-butenedioate (2:1) 2-[2-(4-dibenzo[b,f][1,4]thiazepin-11-yl-1-piperazinyl)ethoxy]ethanol hemifumarate QUETIAPINE FUMARATE DIBENZOTHIAZEPINOHONEP ICI-204636 QUETIAPINE FUMARATE, 99+% Quetiapine Fumarate main intermediates Seroquel, ICI-204636, Dibenzothiazepinohonep QUETIAPINE HEMIGUMARTE Quetiapine·0.5fumaric acid 2-[2-(4-{2-thia-9-azatricyclo[9.4.0.0^{3,8}]pentadeca-1(15),3,5,7,9,11,13-heptaen-10-yl}piperazin-1-yl)ethoxy]ethan-1-ol Quetiapine fuMarate(Seroquel) 2-[2-(4-Dibenzo[b,f][1,4]thiazepin-11-yl-1-piperazinyl)ethoxy]ethanol Bis[(2E)-2-Butenedioate] Quetiapine FuMarate API Quetiapine hemifumarate saL Quetiapine Fumarate RS Quetiapine for system suitability CRS Quetiapine Fumarate (200 mg) QuetiapineHemifumarate> Quetiapine fumarate CRS Quitiapine Fumarate Quetiapine fumarate USP/EP/BP Quetiapine fumarate salt Quetine fumarate Quetiapine Fumarate (ICI 204636)) Quetiapine D4 HemifumarateQ: What is Quetiapine D4 Hemifumarate Q: What is the CAS Number of Quetiapine D4 Hemifumarate Q: What is the storage condition of Quetiapine D4 Hemifumarate Q: What are the applications of Quetiapine D4 Hemifumarate Quetiapine for system suitability (Y0001419) Quetiapine fumarate (Y0001657) Quetiapine fumarateQ: What is Quetiapine fumarate Q: What is the CAS Number of Quetiapine fumarate Q: What is the storage condition of Quetiapine fumarate Quetiapine Fumarate (1592704) Quetinapine Fumarate Quintiapine fumarate Quetiapine Fumarate IP/BP/EP/USP Quetiapine Fumarate 2-[2-(4-dibenzo[b,f][1,4]thiazepin-11-yl-1- piperazinyl)ethoxy]ethanol hemifumarate QuetiapineFumarate(BP) Quetiapine Fumarate Quetiapine Hemifumarate Quetiapine Fumerate- IHS/IP Quetiapine hemifumarate in methanol Quetiapine hemifumarate, D2 and 5-HT2 antagonis Quetiapine hemifumarate, 10 mM in DMSO QUETIAPINE HEMIFUMARATE (NON-STERILE BULK DRUG SUBSTANCE) Quetiapine (ICI-204636) fumarate Q3638 Quetiapine hemifumarate salt【Q3638】 Quetiapine.hemifumarate, 1mg/ml in Methanol (as free base) Quetiapine Fumarate 1.0 mg/ml in Methanol (as free base) Quetiapine hemifumarate: 2-2-(4-Dibenzo[b,f ][1,4] thiazepin-11-ylpiperazin-1-yl) ethoxyethanol hemifumarate