GSK334429 hydrochloride
GSK334429 hydrochloride (CAS: 799558-94-4) is a white to beige powder with a molecular weight of 398.47 (free base basis). This compound is primarily utilised as an antagonist in cell biology and neuroscience research. Its chemical structure is 1-(1-Methylethyl)-4-((1-(6-(trifluoromethyl)-3-pyridinyl)-4-piperidinyl)carbonyl)hexahydro-1H-1,4-diazepine hydrochloride. It exhibits solubility in water at 5 mg/mL.
- IUPAC
- 1-(1-Methylethyl)-4-((1-(6-(trifluoromethyl)-3-pyridinyl)-4-piperidinyl)carbonyl)hexahydro-1H-1,4-diazepine hydrochloride

Neuroscience Research
GSK334429 hydrochloride serves as a valuable tool in neuroscience research, particularly for investigating neurotransmission and cell signaling pathways. Its antagonistic properties aid in understanding receptor function and neuronal communication.
Cell Biology Studies
This compound is employed in cell biology to study cellular responses and signaling mechanisms. As an antagonist, it helps researchers elucidate the roles of specific molecular targets within cellular processes.
Pharmacological Investigation
GSK334429 hydrochloride is utilised for its antagonistic activity in pharmacological studies. It enables the examination of drug interactions and the development of new therapeutic strategies by targeting specific biological pathways.
| Molecular weight | 398.47 (free base basis) |
|---|---|
| Empirical formula | C20H29F3N4O · xHCl |
| Assay | ≥98% (HPLC) |
| Form | powder |
| Colour | white to beige |
| Solubility | H2O: soluble5 mg/mL (clear solution) |
| Storage temperature | 2-8°C |
| Storage Condition | desiccated |
|---|
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is GSK334429 hydrochloride used for?
+
GSK334429 hydrochloride is used as an antagonist in neuroscience and cell biology research, particularly for studying cell signaling and neurotransmission.
What is the CAS number and formula for GSK334429 hydrochloride?
+
The CAS number is 799558-94-4. The empirical formula is C20H29F3N4O · xHCl.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies GSK334429 hydrochloride with a purity of ≥98% by HPLC. This compound is supplied for research purposes and is not represented as USP, BP, EP, or any other pharmacopoeia grade.
What are the safety and handling precautions for GSK334429 hydrochloride?
+
GSK334429 hydrochloride is classified under WGK Germany 3, indicating it is hazardous to water. Handle with appropriate personal protective equipment in a well-ventilated area. Avoid release into the environment.
How is GSK334429 hydrochloride shipped and exported?
+
Tech Serve Solutions is a specialist global supplier and exporter of fine chemicals, ensuring appropriate packaging and documentation for international shipment of GSK334429 hydrochloride.
How can I request a sample or quote for GSK334429 hydrochloride?
+
To request a sample or obtain a quote for GSK334429 hydrochloride, please contact our sales team through the provided channels on the Tech Serve Solutions website.
▶ Related products

(−)-Curcumol
C15H24O2
Cell Biology
(±) Clopidogrel hydrogensulfate
Cell Biology

(±)-L-Alliin
C6H11NO3S
Cell Biology
(±)-2-Amino-4-phosphonobutyric acid
C4H10NO5P
Cell Biology
(±)-2-Methylarachidonoyl-2′-fluoroethylamide
C23H38NOF
Cell Biology
(±)-3,4-Methylenedioxy-N-ethylamphetamine hydrochloride
Cell Biology

(±)-3,4-Methylenedioxyamphetamine hydrochloride
Cell Biology

(±)-3,4-Methylenedioxymethamphetamine hydrochloride
Cell Biology
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis