3-(2-Hydroxyphenyl)propionic acid

CAS No. 495-78-3

3-(2-Hydroxyphenyl)propionic acid ( —— )

Catalog No. M19688 CAS No. 495-78-3

3-(2-Hydroxyphenyl)propanoic acid also known as melilotic acid or melilotate. Within the cell 3-(2-hydroxyphenyl)propanoic acid is primarily located in the cytoplasm. 3-(2-Hydroxyphenyl)propanoic acid can be biosynthesized from propionic acid.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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500MG 26 In Stock
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Biological Information

  • Product Name
    3-(2-Hydroxyphenyl)propionic acid
  • Note
    Research use only not for human use.
  • Brief Description
    3-(2-Hydroxyphenyl)propanoic acid also known as melilotic acid or melilotate. Within the cell 3-(2-hydroxyphenyl)propanoic acid is primarily located in the cytoplasm. 3-(2-Hydroxyphenyl)propanoic acid can be biosynthesized from propionic acid.
  • Description
    3-(2-Hydroxyphenyl)propanoic acid also known as melilotic acid or melilotate. Within the cell 3-(2-hydroxyphenyl)propanoic acid is primarily located in the cytoplasm. 3-(2-Hydroxyphenyl)propanoic acid can be biosynthesized from propionic acid. Outside of the human body 3-(2-hydroxyphenyl)propanoic acid can be found in a number of food items such as herbs and spices red beetroot chinese cinnamon and bilberry. This makes 3-(2-hydroxyphenyl)propanoic acid a potential biomarker for the consumption of these food products.
  • Synonyms
    ——
  • Pathway
    Proteasome/Ubiquitin
  • Target
    Endogenous Metabolite
  • Recptor
    Human Endogenous Metabolite
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    495-78-3
  • Formula Weight
    166.17
  • Molecular Formula
    C9H10O3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:10 mM
  • SMILES
    OC(=O)CCc1ccccc1O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Sinha R Ahn J Sampson J N et al. Fecal Microbiota Fecal Metabolome and Colorectal Cancer Interrelations[J]. PLOS ONE 2016 11(3):e0152126.
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