Chemical Name: 6-Chloro-2,3,4,5-tetrahydro-1-phenyl-3-(2-propen-1-yl)-1H-3-benzazepine-7,8-diol hydrobromide
Purity: ≥98% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
D1 agonist. Increases renal blood flow in animal models and promotes contralateral rotation in rats with unilateral lesions of the substantia nigra. Also augments GABAB inhibitory post-synaptic potentials (ipsp) in ventral tegmental area in brain slices.
Technical Data
M. Wt
410.73
Formula
C19H20ClNO2.HBr
Storage
Store at RT
Purity
≥98% (HPLC)
CAS Number
74115-01-8
PubChem ID
9909521
InChI Key
WLXGFAVTAAQOFH-UHFFFAOYSA-N
Smiles
OC1=CC(C(C2=CC=CC=C2)CN(CC=C)CC3)=C3C(Cl)=C1O.Br
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
DMSO
41.07
100
water
2.05
5mM with gentle warming
Preparing Stock Solutions
The following data is based on the product molecular weight 410.73. 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
2.43 mL
12.17 mL
24.35 mL
5 mM
0.49 mL
2.43 mL
4.87 mL
10 mM
0.24 mL
1.22 mL
2.43 mL
50 mM
0.05 mL
0.24 mL
0.49 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
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References
References are publications that support the products' biological activity.
Pfeifferet al (1982) Dopaminergic activity of substituted 6-chloro-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepines. J.Med.Chem. 25 352 PMID: 7069713
Cameron and Williams
(1993) Dopamine D1 receptors facilitate transmitter release. Nature 366 344 PMID: 8247128