Basic information Safety Supplier Related

8-OH-DPAT·hydrobromide

Basic information Safety Supplier Related

8-OH-DPAT·hydrobromide Basic information

Product Name:
8-OH-DPAT·hydrobromide
Synonyms:
  • 3-(Dipropylamino)tetralin-5-ol·hydrobrominate
  • Serotonin agonist DPAT
  • rac-8-Hydroxy-2-dipropylaMinotetralin HydrobroMide
  • (+/-)-8-Hydroxy(N,N-dipropyl-2-aMino)tetralin HydrobroMide
  • 7-(DipropylaMino)-5,6,7,8-tetrahydro-1-naphthalenol HydrobroMide
  • 8-OH-DPAT HRr
  • 7-(dipropylamino)-5,6,7,8-tetrahydronaphthalen-1-ol hydrobromide
  • 7-(dipropylamino)-5,6,7,8-tetrahydronaphthalen-1-ol hydrobromide76135-31-4
CAS:
76135-31-4
MF:
C16H25NO.BrH
MW:
328.29
Product Categories:
  • Agonist
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
Mol File:
76135-31-4.mol
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8-OH-DPAT·hydrobromide Chemical Properties

Melting point:
221.5-222.0 °C
storage temp. 
Desiccate at +4°C
solubility 
Soluble to 20 mM in water with gentle warming
form 
Powder
color 
White to off-white
EPA Substance Registry System
1-Naphthalenol, 7-(dipropylamino)-5,6,7,8-tetrahydro-, hydrobromide (1:1) (76135-31-4)
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Safety Information

HS Code 
2921199990
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8-OH-DPAT·hydrobromide Usage And Synthesis

Uses

Dopamine receptor Agonist.

Biological Activity

The standard selective 5-HT1A agonist. Also has moderate affinity for 5-HT7 receptors (pKi is 6.6 at the human 5-HT7 receptor expressed in HEK 293 cells). Reduces hippocampal 5-HT levels following systemic administration in rats in vivo.

in vivo

8-OH-DPAT (8-Hydroxy-DPAT) hydrobromide (32, 56, 80, 100 mg/kg; intramuscularly; 15 min prior to the testing session) of the highest dose significantly interferes with sustained attention and reinforcer efficacy (progressive ratio; PR) performance in the 3,4-methylenedioxymethamphetamine (MDMA)-exposed but not control animals[1].

IC 50

5-HT1A Receptor: 8.19 (pIC50)

storage

Desiccate at +4°C

8-OH-DPAT·hydrobromideSupplier

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