Dibenzylpiperazine

Source: Wikipedia, the free encyclopedia.
Dibenzylpiperazine
Names
Preferred IUPAC name
1,4-Dibenzylpiperazine
Other names
DBZP
Identifiers
3D model (
JSmol
)
ChemSpider
ECHA InfoCard
100.153.085 Edit this at Wikidata
UNII
  • InChI=1S/C18H22N2/c1-3-7-17(8-4-1)15-19-11-13-20(14-12-19)16-18-9-5-2-6-10-18/h1-10H,11-16H2 ☒N
    Key: YPUGLZQRXQQCSX-UHFFFAOYSA-N ☒N
  • InChI=1/C18H22N2/c1-3-7-17(8-4-1)15-19-11-13-20(14-12-19)16-18-9-5-2-6-10-18/h1-10H,11-16H2
    Key: YPUGLZQRXQQCSX-UHFFFAOYAP
  • C1CN(CCN1CC2=CC=CC=C2)CC3=CC=CC=C3
  • c1ccc(cc1)CN2CCN(CC2)Cc3ccccc3
Properties
C18H22N2
Molar mass 266.388 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Dibenzylpiperazine (DBZP) is a

byproduct during BZP synthesis, either because the reaction has been run at too high a temperature, or because an excess of benzyl chloride
has been used.

Pharmacology and effects

It is not known to have any stimulant effects in its own right, although this has not been tested.

Toxicity

The toxicity of DBZP is unknown.

Legal status

China

As of October 2015 DBZP is a controlled substance in China.[2]

United States

DBZP is not scheduled as a

Federal Analog Act
.

Florida

DBZP is a

Schedule I controlled substance in the state of Florida making it illegal to buy, sell, or possess in Florida.[4]

See also

References

  1. PMID 20413562
    .
  2. ^ "关于印发《非药用类麻醉药品和精神药品列管办法》的通知" (in Chinese). China Food and Drug Administration. 27 September 2015. Archived from the original on 1 October 2015. Retrieved 1 October 2015.
  3. ^ "21 CFR — Schedules of Controlled Substances §1308.11 Schedule I." Archived from the original on 2009-08-27. Retrieved 2014-12-17.
  4. ^ "Florida Statutes - Chapter 893 - Drug Abuse Prevention and Control".