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3,4,5-Trimethoxycinnamyl alcohol

CAS# 30273-62-2

3,4,5-Trimethoxycinnamyl alcohol

Catalog No. BCN5212----Order now to get a substantial discount!

Product Name & Size Price Stock
3,4,5-Trimethoxycinnamyl alcohol: 5mg $477 In Stock
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Quality Control of 3,4,5-Trimethoxycinnamyl alcohol

Number of papers citing our products

Chemical structure

3,4,5-Trimethoxycinnamyl alcohol

3D structure

Chemical Properties of 3,4,5-Trimethoxycinnamyl alcohol

Cas No. 30273-62-2 SDF Download SDF
PubChem ID 6436306 Appearance Oil
Formula C12H16O4 M.Wt 224.3
Type of Compound Phenylpropanoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (E)-3-(3,4,5-trimethoxyphenyl)prop-2-en-1-ol
SMILES COC1=CC(=CC(=C1OC)OC)C=CCO
Standard InChIKey HZDDMDAKGIRCPP-SNAWJCMRSA-N
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.

Source of 3,4,5-Trimethoxycinnamyl alcohol

The root of Acorus gramineus.

Biological Activity of 3,4,5-Trimethoxycinnamyl alcohol

Description1. 3,4,5-Trimethoxycinnamyl alcohol shows significant antimicrobial and cytotoxic activities.
TargetsAntifection

3,4,5-Trimethoxycinnamyl alcohol Dilution Calculator

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3,4,5-Trimethoxycinnamyl alcohol Molarity Calculator

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Preparing Stock Solutions of 3,4,5-Trimethoxycinnamyl alcohol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.4583 mL 22.2916 mL 44.5831 mL 89.1663 mL 111.4579 mL
5 mM 0.8917 mL 4.4583 mL 8.9166 mL 17.8333 mL 22.2916 mL
10 mM 0.4458 mL 2.2292 mL 4.4583 mL 8.9166 mL 11.1458 mL
50 mM 0.0892 mL 0.4458 mL 0.8917 mL 1.7833 mL 2.2292 mL
100 mM 0.0446 mL 0.2229 mL 0.4458 mL 0.8917 mL 1.1146 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 3,4,5-Trimethoxycinnamyl alcohol

Antimicrobial and cytotoxic constituents of Loranthus globosus.[Pubmed:12727502]

Fitoterapia. 2003 Apr;74(3):308-11.

(+)-Catechin, 3,4-dimethoxycinnamyl alcohol and 3,4,5-Trimethoxycinnamyl alcohol were isolated from the barks of Loranthus globosus. All compounds showed significant antimicrobial and cytotoxic activities.

Toxicological studies of two compounds isolated from Loranthus globosus Roxb.[Pubmed:19093449]

Pak J Biol Sci. 2007 Jun 15;10(12):2073-7.

The sub-acute toxicities of two compounds 3,4-dimethoxycinnamyl alcohol (1) and 3,4,5-Trimethoxycinnamyl alcohol (2) isolated from the plant Loranthus globosus Roxb were studied on long Evan's rats. The studies included the gross general observation such as changes in body weight, haematological profiles [total count of Red Blood Cells (RBC) and White Blood Cells (WBC), differential count of WBC, platelet count and Haemoglobin (Hb)%], biochemical parameters of blood [Serum Glutamate Oxaloacetate Transaminase (SGOT), Serum Glutamate Pyruvate Transaminase (SGPT), Serum Alkaline Phosphatase (SALP), urea and creatinine) and histopathology of the liver, kidney, heart and lung of both control and experimental groups of rats. The changes in haematological and biochemical parameters were statistically not significant after the administration of compounds 1 and 2 in a dose of 300 microg/rat/day for consecutive 14 days. No abnormality was found in the histopathology of the liver, kidney, heart and lung in the experimental groups of rats following same dose when compared with control group. This preliminary study suggests that the isolated compounds may be used safely for clinical trial.

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