Cararosinol A

CAS# 651733-57-2

Cararosinol A

Catalog No. BCX1674----Order now to get a substantial discount!

Product Name & Size Price Stock
Cararosinol A: 5mg $740 In Stock
Cararosinol A: 10mg Please Inquire In Stock
Cararosinol A: 20mg Please Inquire Please Inquire
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Quality Control of Cararosinol A

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Chemical structure

Cararosinol A

Chemical Properties of Cararosinol A

Cas No. 651733-57-2 SDF Download SDF
PubChem ID N/A Appearance Powder
Formula C56H42O13 M.Wt 922.92
Type of Compound Other Phenolic Compounds Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Cararosinol A Dilution Calculator

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Cararosinol A Molarity Calculator

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Preparing Stock Solutions of Cararosinol A

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.0835 mL 5.4176 mL 10.8352 mL 21.6704 mL 27.0879 mL
5 mM 0.2167 mL 1.0835 mL 2.167 mL 4.3341 mL 5.4176 mL
10 mM 0.1084 mL 0.5418 mL 1.0835 mL 2.167 mL 2.7088 mL
50 mM 0.0217 mL 0.1084 mL 0.2167 mL 0.4334 mL 0.5418 mL
100 mM 0.0108 mL 0.0542 mL 0.1084 mL 0.2167 mL 0.2709 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on Cararosinol A

[Studies on chemical constituents from roots of Caragana sinica].[Pubmed:18536372]

Zhongguo Zhong Yao Za Zhi. 2008 Mar;33(5):517-21.

OBJECTIVE: To study the chemical constituents in roots of Caragana sinica. METHOD: The constituents were isolated by silica gel column chromatography, and their structures were identified by spectroscopic methods. RESULT: Seven compounds were identified as (+) - stenophyllol B (1), 4-hydroxybenzoic acid (2), odoratin (3), resveratrol (4), Cararosinol A (5), leachinol C (6), carasinaurone (7) respectively. CONCLUSION: Compound 1 was a new compound which was the enantiomer of stenophyllol B. Compounds 2-6 were obtained from the plant for the first time.

[Anti-HIV chemical constituents of aerial parts of Caragana rosea].[Pubmed:17518047]

Yao Xue Xue Bao. 2007 Feb;42(2):179-82.

This study was intended to look for anti-HIV chemical constituents of aerial parts of Caragana rosea Turcz. Column chromatographic technique was used for the isolation and purification of constituents of Caragana rosea under the guide of anti-HIV assay. The structures were established on the basis of physical and chemical properties and spectroscopic data. Five compounds were obtained from the EtOAc fraction of aerial parts of Caragana rosea and identified as myricetin (1), mearnsetin (2), p-hydroxy cinnamic acid (3), Cararosinol A (4) and cararosinol B (5). At the same time, one possible transformation route between cararosinol B and kobophenol A, another resveratrol tetramer isolated from this plant previously, was proposed. Compounds 4, 5 are new resveratrol tetramers, compounds 1 -3 were isolated from this plant for the first time. All compounds showed no activities in an in vitro assay against HIV-1.

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