MedKoo Cat#: 414950 | Name: Piflutixol HCl

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Piflutixol HCl is an Antipsychotic Agent

Chemical Structure

Piflutixol HCl
Piflutixol HCl
CAS#60197-32-2 (HCl)

Theoretical Analysis

MedKoo Cat#: 414950

Name: Piflutixol HCl

CAS#: 60197-32-2 (HCl)

Chemical Formula: C24H26ClF4NOS

Exact Mass:

Molecular Weight: 487.98

Elemental Analysis: C, 59.07; H, 5.37; Cl, 7.26; F, 15.57; N, 2.87; O, 3.28; S, 6.57

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
Bulk Inquiry
Related CAS #
60197-32-2 (HCl); 54341-02-5 (free base)
Synonym
Piflutixol hydrochloride; Piflutixol HCl; NSC 312907; NSC312907; NSC-312907
IUPAC/Chemical Name
4-Piperidineethanol, 1-(3-(6-fluoro-2-trifluoromethyl-9-thioxanthenilidene)propyl)-, hydrochloride
InChi Key
NAPIVRWXCRDUBI-YNZNYVPVSA-N
InChi Code
InChI=1S/C24H25F4NOS.ClH/c25-18-4-5-20-19(2-1-10-29-11-7-16(8-12-29)9-13-30)21-14-17(24(26,27)28)3-6-22(21)31-23(20)15-18;/h2-6,14-16,30H,1,7-13H2;1H/b19-2-;
SMILES Code
OCCC1CCN(CC/C=C2C3=C(SC4=C\2C=CC(F)=C4)C=CC(C(F)(F)F)=C3)CC1.[H]Cl
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 487.98 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Fleminger S. The relationship between the occupation of the D-1 dopamine receptor by [3H]piflutixol and the activity of dopamine-sensitive adenylate cyclase in rat striatal membranes. Biochem Pharmacol. 1991 Jul 5;42(2):229-37. doi: 10.1016/0006-2952(91)90708-d. PMID: 1650205. 2: Nielsen IM, Boeck V, Christensen AV, Danneskiold-Samsoe P, Hyttel J, Langeland J, Pedersen V, Svendsen O. The pharmacology of a new potent, long acting neuroleptic, piflutixol. Acta Pharmacol Toxicol (Copenh). 1977 Oct;41(4):369-83. doi: 10.1111/j.1600-0773.1977.tb02675.x. PMID: 579063. 3: Hyttel J. Similarities between the binding of 3H-piflutixol and 3H-flupentixol to rat striatal dopamine receptors in vitro. Life Sci. 1981 Feb 2;28(5):563-9. doi: 10.1016/0024-3205(81)90150-8. PMID: 6111013. 4: Kilpatrick GJ, Jenner P, Marsden CD. Specific [3H]piflutixol binding to CHAPS-solubilised rat striatal preparations involves dopamine D-2 but not D-1 binding sites. J Neurochem. 1986 Feb;46(2):413-21. doi: 10.1111/j.1471-4159.1986.tb12984.x. PMID: 3941314. 5: Hyttel J. Effect of piflutixol on turnover of catecholamines in mouse brain and rat corpus striatum. Acta Pharmacol Toxicol (Copenh). 1977 Nov;41(5):449-57. doi: 10.1111/j.1600-0773.1977.tb02155.x. PMID: 579556. 6: Jenner P, Boyce S, Marsden CD. Receptor changes during chronic dopaminergic stimulation. J Neural Transm Suppl. 1988;27:161-75. doi: 10.1007/978-3-7091-8954-2_14. PMID: 2900291. 7: O'Boyle KM, Waddington JL. Loss of rat striatal dopamine receptors with ageing is selective for D-2 but not D-1 sites: association with increased non- specific binding of the D-1 ligand [3H]piflutixol. Eur J Pharmacol. 1984 Oct 1;105(1-2):171-4. doi: 10.1016/0014-2999(84)90663-0. PMID: 6149143. 8: Cross A, Rossor M. Dopamine D-1 and D-2 receptors in Huntington's disease. Eur J Pharmacol. 1983 Mar 25;88(2-3):223-9. doi: 10.1016/0014-2999(83)90009-2. PMID: 6221936. 9: O'Boyle KM, Waddington JL. Selective and stereospecific interactions of R-SK & F 38393 with [3H]piflutixol but not [3H]spiperone binding to striatal D1 and D2 dopamine receptors: comparisons with SCH 23390. Eur J Pharmacol. 1984 Mar 2;98(3-4):433-6. doi: 10.1016/0014-2999(84)90294-2. PMID: 6144559. 10: Klimek V, Nielsen M, Maj J. Repeated treatment with imipramine decreased the number of [3H]piflutixol binding sites in the rat striatum. Eur J Pharmacol. 1985 Feb 12;109(1):131-2. doi: 10.1016/0014-2999(85)90551-5. PMID: 2859994.