16-Hydroxy-8(17),13-labdadien-15,16-olid-19-oic acid

16-Hydroxy-8(17),13-labdadien-15,16-olid-19-oic acid
Product Name 16-Hydroxy-8(17),13-labdadien-15,16-olid-19-oic acid
CAS No.: 691009-85-5
Catalog No.: CFN97177
Molecular Formula: C20H28O5
Molecular Weight: 348.4 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Powder
Source: The branches of Platycladus orientalis.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
16-Hydroxy-8(17),13-labdadien-15,16-olid-19-oic acid may show a strong algicidal activity against Raphidocelis subcapitata.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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  • 16-Hydroxy-8(17),13-labdadien-15,16-olid-19-oic acid

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    Phytochemistry (Amsterdam), 2003, 64(7):1309-1317.
    ent-Labdane diterpenes from the aquatic plant Potamogeton pectinatus.[Reference: WebLink]

    METHODS AND RESULTS:
    Four new ent-labdane diterpenes were isolated from the freshwater aquatic plant Potamogeton pectinatus, together with two known furano-ent-labdanes. The new compounds were assigned the structures methyl-15,16-epoxy-12(R)-acetoxy- 8(17),13(16),14-ent-labdatrien-19-oate, 15,16-epoxy-12(R)-acetoxy-8(17),13(16),14-ent-labdatrien-19-oic acid, 8(17),13-ent-labdadien-15 → 16-lactone-19-oic acid and 16-hydroxy-8(17),13-ent-labdadien-15,16-olid-19-oic acid(16-Hydroxy-8(17),13-labdadien-15,16-olid-19-oic acid) by spectroscopic means.
    CONCLUSIONS:
    Some of these labdanes showed a strong algicidal activity against Raphidocelis subcapitata.
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