Alternative Names: 2,5-Dimethoxy-4-bromoamphetamine hydrochloride
Chemical Name: 4-Bromo-2,5-dimethoxy-α-methylbenzeneethanamine hydrochloride
Purity: ≥99% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Selective 5-HT2 receptor agonist (Ki values are 0.44, 59, 69, 831 and 3700 nM for 5-HT2H, 5-HT2L, 5-HT2C, 5-HT1B and 5-HT1A receptors respectively). Hallucinogenic.
Technical Data
M. Wt
310.62
Formula
C11H16BrNO2.HCl
Storage
Store at RT
Purity
≥99% (HPLC)
CAS Number
29705-96-2
PubChem ID
12626562
InChI Key
SPBBKPOIDQIWDZ-UHFFFAOYSA-N
Smiles
BrC1=C(OC)C=C(CC(C)N)C(OC)=C1.Cl
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent
Max Conc. mg/mL
Max Conc. mM
Solubility
water
31.06
100
Preparing Stock Solutions
The following data is based on the product molecular weight 310.62. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
3.22 mL
16.1 mL
32.19 mL
5 mM
0.64 mL
3.22 mL
6.44 mL
10 mM
0.32 mL
1.61 mL
3.22 mL
50 mM
0.06 mL
0.32 mL
0.64 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Titileret al (1987) Selectivity of serotonergic drugs for multiple brain serotonin receptors. Biochem.Pharmacol. 36 3265 PMID: 3663239
Arvanovet al (1999) A pre- and postsynaptic modulatory action of 5-HT and the 5-HT2A,2C receptor agonist DOB on NMDA-evoked responses in the rat medial prefrontal cortex. Eur.J.Neurosci. 11 2917 PMID: 10457188
McKennaet al (1989) Differentiation of 5-hydroxytryptamine2 receptor subtypes using 125I-R-(-)2,5-dimethoxy-4-iodo-phenylisopropylamine and 3H-ketanserin. J.Neurosci. 10 3482 PMID: