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Key Documents

T8948

Sigma-Aldrich

1-(α,α,α-Trifluoro-m-tolyl)piperazine hydrochloride

99%

Synonym(s):

N-[3-(Trifluoromethyl)phenyl]piperazine hydrochloride, TFMPP hydrochloride

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About This Item

Empirical Formula (Hill Notation):
C11H13F3N2 · HCl
CAS Number:
Molecular Weight:
266.69
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77

assay

99%

drug control

regulated under CDSA - not available from Sigma-Aldrich Canada

availability

not available in Japan

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

239-241 °C (lit.)

solubility

methanol:glacial acetic acid (1:1): soluble 25 mg/mL

application(s)

forensics and toxicology
veterinary

SMILES string

Cl.FC(F)(F)c1cccc(c1)N2CCNCC2

InChI

1S/C11H13F3N2.ClH/c12-11(13,14)9-2-1-3-10(8-9)16-6-4-15-5-7-16;/h1-3,8,15H,4-7H2;1H

InChI key

DGNLGWJZZZOYPT-UHFFFAOYSA-N

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Preparation Note

1-(α,α,α-Trifluoro-m-tolyl)piperazine hydrochloride is soluble in methanol:glacial acetic acid (1:1) at 25 mg/ml.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

STOT SE 3

target_organs

Central nervous system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Anne Zwartsen et al.
Neurotoxicology, 66, 87-97 (2018-03-25)
While the prevalence and the use of new psychoactive substances (NPS) is steadily increasing, data on pharmacological, toxicological and clinical effects is limited. Considering the large number of NPS available, there is a clear need for efficient in vitro screening
Ushtana Antia et al.
Journal of forensic sciences, 55(5), 1311-1318 (2010-06-11)
An LC-MS method was developed for benzylpiperazine (BZP) and trifluoromethylphenylpiperazine (TFMPP), constituents of "party pills" or "legal herbal highs," and their metabolites in human blood plasma. Compounds were resolved using a mixture of ammonium formate (pH 4.5, 0.01 M) and

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