CAS No. 69308-37-8

Batch: Purity:99.72
(R)-baclofen Chemical Structure
Chemical Structure
Check the (R)-baclofen product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name (3R)-4-amino-3-(4-chlorophenyl)butanoic acid
CAS Number 69308-37-8
Molecular Formula

C10H12ClNO2

Molecular Weight (MW) 213.66
SMILES C1=CC(=CC=C1C(CC(=O)O)CN)Cl
InChIKey KPYSYYIEGFHWSV-QMMMGPOBSA-N

Ordering Information

Biological Activity

(R)-baclofen is a selective agonist of the metabotropic GABAB receptor that functions as the active enantiomer of baclofen. Activation of GABAB receptor complexes inhibits adenylyl cyclase activity and downregulates voltage-gated calcium channels while activating inwardly rectifying potassium channels. These signaling cascades depress presynaptic neurotransmitter release and hyperpolarize postsynaptic neuronal membranes, leading to suppressed excitatory synaptic transmission and attenuated muscle spasticity. [1]

How to Prepare Stock Solution?

Concentration Volume Mass
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Solubility

Batch:
All in vitro solubility values are batch-tested experimental data (non-literature values).
Solvent Solubility & Note
Water 8 mg/mL
DMSO Insoluble
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)
Ethanol Insoluble
FAQ
Q: Why does a DMSO stock precipitate in media/saline?
A: It is caused by unheated aqueous media (supersaturation), local solvent shock, or incorrect mixing sequence.
How to fix it?
  • Preheat media/saline to 37°C.
  • Mix rapidly (pipette/vortex) upon addition.
  • For complex mixes, always add the aqueous phase last.
  • Re-dissolve minor precipitates with a 37°C water bath and sonication (≤30 min).

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Note: Technical data last updated: Sep 1, 2026.