7-OH-DPAT Hydrobromide
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Hodoodo CAT#: H527758

CAS#: 76135-30-3

Description: 7-OH-DPAT Hydrobromide is a potent and selective Dopamine D3 receptor agonist.


Chemical Structure

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7-OH-DPAT Hydrobromide
CAS# 76135-30-3

Theoretical Analysis

Hodoodo Cat#: H527758
Name: 7-OH-DPAT Hydrobromide
CAS#: 76135-30-3
Chemical Formula: C16H26BrNO
Exact Mass: 327.12
Molecular Weight: 328.294
Elemental Analysis: C, 58.54; H, 7.98; Br, 24.34; N, 4.27; O, 4.87

Price and Availability

Size Price Availability Quantity
5mg USD 220 2 Weeks
10mg USD 360 2 Weeks
25mg USD 620 2 Weeks
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Synonym: 7-OH-DPAT Hydrobromide

IUPAC/Chemical Name: 7-Hydroxy-N,N-dipropyl-2-aminotetralin hydrobromide

InChi Key: ODNDMTWHRYECKX-UHFFFAOYSA-N

InChi Code: InChI=1S/C16H25NO.BrH/c1-3-9-17(10-4-2)15-7-5-13-6-8-16(18)12-14(13)11-15;/h6,8,12,15,18H,3-5,7,9-11H2,1-2H3;1H

SMILES Code: CCCN(CCC)C1CC2=C(C=CC(O)=C2)CC1.[H]Br

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: Soluble in DMSO

Shelf Life: >2 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

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:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 328.29 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
Formulation protocol:
In vitro protocol:
In vivo protocol:

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