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R(+)-Baclofen hydrochloride

SIGMA/G013 - solid

Synonym: Arbaclofen hydrochloride; R(+)-β-(Aminomethyl)-4-chlorobenzenepropanoic acid hydrochloride; STX209

CAS Number: 63701-55-3
Empirical Formula (Hill Notation): C10H12ClNO2 · HCl
Molecular Weight: 250.12
MDL Number: MFCD00078579
Linear Formula: C10H12ClNO2 · HCl
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-G013-25MG 25 mg
$242.00
1/EA
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45-G013-100MG 100 mg
$757.00
1/EA
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45-G013-500MG 500 mg
$2820.00
1/EA
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color white
form solid
InChI 1S/C10H12ClNO2.ClH/c11-9-3-1-7(2-4-9)8(6-12)5-10(13)14;/h1-4,8H,5-6,12H2,(H,13,14);1H/t8-;/m0./s1
InChI key WMNUVYYLMCMHLU-QRPNPIFTSA-N
optical activity [α]28/D +3.8°, c = 0.9 in methanol(lit.)
Quality Level 100 
SMILES string Cl[H].NC[C@H](CC(O)=O)c1ccc(Cl)cc1
solubility DMSO: >20 mg/mL
  H2O: 26 mg/mL (Solutions may be stored for several weeks at 4 °C.)
storage condition desiccated
Application: R(+)-Baclofen hydrochloride has been used as a GABAB receptor agonist to study its effects on M43068-induced antinociception in rat models. It has also been used as a GABAB receptor agonist to study its effects on amphetamine-induced behavior and neurochemical responses in rat striatum.
Biochem/physiol Actions: Baclofen is a derivative of γ-aminobutyric acid (GABA) and acts as a 4-aminobutanoic acid receptor (GABAB) agonist. It interacts stereospecifically with the GABA receptor and exhibits antispastic effects.Baclofen shows therapeutic effects against paroxysmal pain of trigeminal neuralgia and spinal spasticity. R(+)-Baclofen is a more active enantiomer.
Other Notes: Same enantiomer as R(−)-baclofen free base.
Packaging: 25, 100, 500 mg in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
UNSPSC 12352200

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