Trifluoperazine Dihydrochloride - ≥98%(HPLC)(T) , Serotonin 2c (5-HT2c) receptor antagonist, CAS No.440-17-5, Serotonin 2c (5-HT2c) receptor antagonist

CAS: 440-17-5 Cat. No.: T162449 Molecular Weight: 480.42 Beilstein Registry Number: 3820020 EC Number: 207-123-0 PubChem CID: 66064
AVAILABLE TO ORDER
GRADE & PURITY ≥98%(HPLC)(T)
Synonyms
D00799 | EU-0101232 | AI3-50137 | Jatroneural | MFCD00012656 | NSC17474 | Triphthasine | EN300-122645 | FT-0600798 | TRIFLUOPERAZINE HYDROCHLORIDE [WHO-DD] | NCGC00094474-01 | NCGC00094474-02 | HY-B0532A | SKF-5019 | TRIFLUOPERAZINE HYDROCHLORIDE (EP MONO
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
T162449-1g
3
$24.90
5g
T162449-5g
1
$92.90
25g
T162449-25g
1
$280.90
100g
T162449-100g
1
$1,008.90
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98%(HPLC)(T) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Trifluoperazine dihydrochloride has been used as a calmodulin kinase antagonist in cultured Aplysia californica neurons. Trifluoperazine dihydrochloride has also been used as a PMCA inhibitor in mouse duodenal tissues to block the transcellular active calcium flux。

Specifications

Synonyms
D00799 | EU-0101232 | AI3-50137 | Jatroneural | MFCD00012656 | NSC17474 | Triphthasine | EN300-122645 | FT-0600798 | TRIFLUOPERAZINE HYDROCHLORIDE [WHO-DD] | NCGC00094474-01 | NCGC00094474-02 | HY-B0532A | SKF-5019 | TRIFLUOPERAZINE HYDROCHLORIDE (EP MONO
Specifications & Purity
≥98%(HPLC)(T)
Biochemical and Physiological Mechanisms
Phenothiazine antipsychotic; D2 dopamine receptor antagonist; inhibits calmodulin-dependent stimulation of 3′:5′-cyclic nucleotide phosphodiesterase; inhibits cAMP-gated cation channels.Cell-permeable calmodulin antagonist. Dopamine receptor antagonist. S
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
ANTAGONIST
Mechanism of action
Serotonin 2c (5-HT2c) receptor antagonist
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Purity
≥98%(HPLC)(T)
Names and Identifiers
Pubchem Sid504754031
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504754031
Canonical SmilesCN1CCN(CC1)CCCN2C3=CC=CC=C3SC4=C2C=C(C=C4)C(F)(F)F.Cl.Cl
IUPAC Name10-[3-(4-methylpiperazin-1-yl)propyl]-2-(trifluoromethyl)phenothiazine;dihydrochloride
InChIKeyBXDAOUXDMHXPDI-UHFFFAOYSA-N
INCHI1S/C21H24F3N3S.2ClH/c1-25-11-13-26(14-12-25)9-4-10-27-17-5-2-3-6-19(17)28-20-8-7-16(15-18(20)27)21(22,23)24;;/h2-3,5-8,15H,4,9-14H2,1H3;2*1H
Isomeric SMILES CN1CCN(CC1)CCCN2C3=CC=CC=C3SC4=C2C=C(C=C4)C(F)(F)F.Cl.Cl
WGK Germany 3
RTECS SP1750000
PubChem CID 66064
Molecular Weight 480.42
Beilstein 3820020
Reaxy-Rn 3820024

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassBenzothiazines
SubclassPhenothiazines
Intermediate Tree Nodes Not available
Direct ParentPhenothiazines
Alternative Parents Alkyldiarylamines  Diarylthioethers  N-methylpiperazines  Benzenoids  1,4-thiazines  Trialkylamines  Azacyclic compounds  Organopnictogen compounds  Organofluorides  Hydrochlorides  Hydrocarbon derivatives  Alkyl fluorides  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Phenothiazine - Alkyldiarylamine - Diarylthioether - Aryl thioether - Tertiary aliphatic/aromatic amine - N-alkylpiperazine - N-methylpiperazine - Para-thiazine - 1,4-diazinane - Piperazine - Benzenoid - Tertiary aliphatic amine - Tertiary amine - Azacycle - Thioether - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organofluoride - Organohalogen compound - Organopnictogen compound - Amine - Alkyl halide - Hydrochloride - Alkyl fluoride - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as phenothiazines. These are polycyclic aromatic compounds containing a phenothiazine moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a para-thiazine ring.
External Descriptors hydrochloride
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CYP1A2 Tchem Cytochrome P450 1A2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CYP2D6 Tclin Cytochrome P450 2D6 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
EBPL Tchem Emopamil-binding protein-like (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
EBP Tchem 3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SIGMAR1 Tclin Sigma non-opioid intracellular receptor 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CALM1 Tclin Calmodulin-1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
KCNH2 Tclin Potassium voltage-gated channel subfamily H member 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DHCR24 Tchem Delta(24)-sterol reductase (295 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SC5D Tbio Lathosterol oxidase (2 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot NumberCertificate TypeDateItem
C2204030Certificate of AnalysisDec 12, 2025 T162449
D2422068Certificate of AnalysisApr 24, 2024 T162449
C1921075Certificate of AnalysisJan 11, 2023 T162449
L2212323Certificate of AnalysisDec 14, 2022 T162449
Chemical and Physical Properties
SolubilitySolubility in water: Completely soluble; Insoluble in Benzene,Ether
SensitivityHeat Sensitive
Melt Point(°C)243°C
Molecular Weight480.400 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count7
Rotatable Bond Count4
Exact Mass479.118 Da
Monoisotopic Mass479.118 Da
Topological Polar Surface Area35.000 Ų
Heavy Atom Count30
Formal Charge0
Complexity510.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
Documents & Articles
Citations of This Product
References
1. Yunfeng Ma, Longxia Li, Liufang Mo, Xiaochen Wang, Chenyue Liu, Yijun Wu, Chaoqun Liu.  (2023)  Preparation and anti-tumor effects of mesoporous silica nanoparticles loaded with trifluoperazine.  Journal of Materials Chemistry B,  11  (43): (10395-10403).  [PMID:37876312] [10.1039/D3TB01472J]
2. Qiang Hou, Yali Wang, Jian Hu, Jianxiong Zhang, Caihua Zhang, Wang Song, Xuesong Wang, Baiqin Zheng, Xin Zhou.  (2024)  Simultaneous determination of phenothiazine drugs and their metabolites residues in animal derived foods by high performance liquid chromatography tandem mass spectrometry.  FOOD CONTROL,      [PMID:] [10.1016/j.foodcont.2024.110799]
Solution Calculators
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