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Cat. No.: HY-187152

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Urushiol (15:2)

Urushiol (15:2) is a 3-substituted catechol with a 15-carbon side chain containing 2 double bonds, and it exists in the sap, bark and lacquer fluid of Rhus vernicifera and Toxicodendron vernicifluum. Urushiol (15:2) is used for research on cancer, fungal infections, bacterial infections and allergic contact dermatitis.

Nos produits utilisent uniquement pour la recherche. Nous ne vendons pas aux patients.

CAS No.: 83258-37-1
Formule: C₂₁H₃₂O₂
Masse moléculaire:316.49

Stockage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (267 KB)

Urushiol (15:2) Chemical Structure

CAS No.: 83258-37-1

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Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Activité biologique
- Description
- In Vitro
Chemical Information
Pureté et documentation
Références
Calculators
Help & FAQs
Classifications
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Activité biologique

Description

In Vitro

Urushiol (15:2) (compound 6) is detectable and quantifiable via reverse-phase HPLC with defined retention times, a response factor of 1.23 × 10^-3, an LOD of 0.57 μg/mL, and an LOQ of 1.90 μg/mL^[4].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Related Protocols :

Chemical Information

CAS No. 83258-37-1
Masse moléculaire 316.49
Formule C₂₁H₃₂O₂
SMILES

C(CCCCCC/C=C\C/C=C\CCC)C1=C(O)C(O)=CC=C1
Livraison

Room temperature in continental US; may vary elsewhere.
Stockage

Please store the product under the recommended conditions in the Certificate of Analysis.

Pureté et documentation

Select Batch:

Pureté: 99.98%

Assay: 99.98%

ee.: 99.98%

Fiche technique (267 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Instruction de manipulation (2659 KB)

Références

[1]. Kamiya Y, et al. Synthesis of urushiol components and analysis of urushi sap from Rhus vernicifera. J Oleo Sci. 2001;50(11):865–874.

[2]. Lee Y, et al. Quantitative Detection of Thitsiol and Urushiol as Markers from the Gluta usitata Lacquer Tree Using HPLC. Molecules. 2023 Dec 26;29(1):149. [Content Brief]

[3]. Chen H, et al. Vortex-blending matrix solid-phase dispersion and UPLC-Q-TOF/MS were proposed to extract and examine the urushiols from Toxicodendron vernicifluum bark. Journal of pharmaceutical and biomedical analysis. 2024 May 15;242:116066. [Content Brief]

[4]. Yu HH, et al. HPLC and ToF‒SIMS Analyses of Toxicodendron vernicifluum Tree Sap Mixed with Other Natural Lacquers. Molecules. 2021 Jan 15;26(2):434. [Content Brief]

Calculators

Calculateur de molarité

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

Calculateur de dilution

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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MOQ

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100 mg

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