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Eucalyptolic acid
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Product Name Eucalyptolic acid
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CAS No.: 189272-68-2
Catalog No.: CFN92275
Molecular Formula: C40H56O7
Molecular Weight: 648.9 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Source: The branches of Eucalyptus globulus
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF
Similar structural: Comparison (Web)  (SDF)
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: Eucalyptolic acid is a natural product from Eucalyptus globulus.
Eucalyptolic acid Description
Source: The branches of Eucalyptus globulus
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: 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

After receiving: 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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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.5411 mL 7.7053 mL 15.4107 mL 30.8214 mL 38.5267 mL
5 mM 0.3082 mL 1.5411 mL 3.0821 mL 6.1643 mL 7.7053 mL
10 mM 0.1541 mL 0.7705 mL 1.5411 mL 3.0821 mL 3.8527 mL
50 mM 0.0308 mL 0.1541 mL 0.3082 mL 0.6164 mL 0.7705 mL
100 mM 0.0154 mL 0.0771 mL 0.1541 mL 0.3082 mL 0.3853 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Structure Identification:
Planta Medica, 1997 , 63 (01) :47-50.
Isolation and Structural Elucidation of Acylated Pentacyclic Triterpenoids from the Leaves of Eucalyptus camaldulensis var. obtusa[Reference: WebLink]

METHODS AND RESULTS:
Ten pentacyclic triterpenoids including two new constituents, eucalyptic acid and Eucalyptolic acid, and eight known compounds (ursolic acid lactone, betulinic acid, oleanolic acid, ursolic acid, 3 beta-O-cis-p-coumaroylalphitolic acid, alphitolic acid, 3 beta-O-trans-p-coumaroylalphitolic add, and 3 beta-O-trans-p-coumaroylmaslinic acid) have been isolated from the fresh and uncrushed leaves of Eucalyptus camaldulensis var. obtuse. Their structures were elucidated through detailed 1D and 2D NMR studies. The new natural products were characterized as 2 alpha-hydroxy-3 beta-E-feruloyloxy-lup-20(29)-en-28-oic acid and 2 alpha-hydroxy-3 beta-E-feruloyloxy-olean-12-en-28-oic acid, respectively.
CONCLUSIONS:
Except for oleanolic acid, all the known compounds are hitherto unreported from this plant. This is the first report of the isolation of 2-oxygenated 3-O-acylated triterpenoids from Eucalyptus genus.
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Kurarinone

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