An inactive metabolite of baclofen
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Parent Compound(s)
18600(±)-Baclofen
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3-(4-Chlorophenyl)-4-hydroxybutyric Acid (sodium salt)

Item No. 21483

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
4-chloro-β-(hydroxymethyl)-benzenepropanoic acid, monosodium salt
CAS Number
1346603-21-1
Synonyms
  • γ-Hydroxybaclofen
Molecular Formula
C10H11ClO3 • Na
Formula Weight
237.6
Purity
≥98%
Formulation (Request formulation change)
A solid
Solubility(Learn about Variance in Solubility)
Methanol: solubleWater: soluble
SMILES
ClC1=CC=C(C(CC(O)=O)CO)C=C1.[Na]
InChi Code
InChI=1S/C10H11ClO3.Na/c11-9-3-1-7(2-4-9)8(6-12)5-10(13)14;/h1-4,8,12H,5-6H2,(H,13,14);
InChi Key
PKWMRTYJSOAALK-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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Certificates of Analysis & Batch Specific Data

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    2.5 mg

    $341

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    Product Description

    3-(4-Chlorophenyl)-4-hydroxybutyric acid is an inactive metabolite of the GABAB receptor agonist baclofen (Item No. 18600).1,2,3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Wuis, E.W., van Beijsterveldt, L.E., Dirks, R.J., et al. Rapid simultaneous determination of baclofen and its γ-hydroxy metabolite in urine by high-performance liquid chromatography with ultraviolet detection. J. Chromatogr. 420(1), 212-216 (1987).

    2. Chéramy, A., Nieoullon, A., and Glowinski, J. Effects of the unilateral nigral application of baclofen on dopamine release in the two caudate nuclei of the cat. Eur. J. Pharmacol. 58(2), 133-140 (1979).

    3. Ault, B., and Evans, R.H. The depressant action of baclofen on the isolated spinal cord of the neonatal rat. Eur. J. Pharmacol. 71(4), 357-364 (1981).