Glucovanillin

CAS No. 494-08-6

Glucovanillin( Vanillin 4-O-β-D-Glucoside )

Catalog No. M21276 CAS No. 494-08-6

Glucovanillin belongs to the class of organic compounds known as phenolic glycosides.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 28 In Stock
10MG 29 In Stock
25MG 61 In Stock
50MG 99 In Stock
100MG 157 In Stock
200MG 235 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Glucovanillin
  • Note
    Research use only, not for human use.
  • Brief Description
    Glucovanillin belongs to the class of organic compounds known as phenolic glycosides.
  • Description
    Glucovanillin belongs to the class of organic compounds known as phenolic glycosides.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Vanillin 4-O-β-D-Glucoside
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    494-08-6
  • Formula Weight
    314.29
  • Molecular Formula
    C14H18O8
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (318.18 mM)
  • SMILES
    COc(cc(C=O)cc1)c1O[C@@H]([C@@H]([C@H]1O)O)O[C@H](CO)[C@H]1O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Chen Y Gu F Li J et al. Involvement of Colonizing Bacillus Isolates in Glucovanillin Hydrolysis during the Curing of Vanilla planifolia Andrews[J]. Applied & Environmental Microbiology 2015 81(15):4947-4954.
molnova catalog
related products
  • Bilirubin

    Extracted from bezoar;Store the product in sealed, cool and dry condition.

  • Usaramine

    Usaramine demonstrates phytotoxicity against Lactuca sativa var. Carrascoy (lettuce) assessed as inhibition of seed germination at 50 ug/cm2 after 24 hr.

  • Azido-PEG9-azide

    Azido-PEG9-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.