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Alizarin 1-methyl ether

CAS#  6170-06-5

Alizarin 1-methyl ether

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Chemical structure

Alizarin 1-methyl ether

3D structure

Chemical Properties of Alizarin 1-methyl ether

Cas No.  6170-06-5 SDF Download SDF
PubChem ID 80309 Appearance Powder
Formula C15H10O4 M.Wt 254.24
Type of Compound Quinones Storage Desiccate at -20°C
Synonyms 2-hydroxy-1-methoxy-anthraquinone
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 2-hydroxy-1-methoxyanthracene-9,10-dione
SMILES COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3C2=O)O
Standard InChIKey VRGZEPNGEFBVIZ-UHFFFAOYSA-N
Standard InChI InChI=1S/C15H10O4/c1-19-15-11(16)7-6-10-12(15)14(18)9-5-3-2-4-8(9)13(10)17/h2-7,16H,1H3
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.

Alizarin 1-methyl ether Dilution Calculator

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Alizarin 1-methyl ether Molarity Calculator

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Preparing Stock Solutions of Alizarin 1-methyl ether

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.9333 mL 19.6665 mL 39.3329 mL 78.6658 mL 98.3323 mL
5 mM 0.7867 mL 3.9333 mL 7.8666 mL 15.7332 mL 19.6665 mL
10 mM 0.3933 mL 1.9666 mL 3.9333 mL 7.8666 mL 9.8332 mL
50 mM 0.0787 mL 0.3933 mL 0.7867 mL 1.5733 mL 1.9666 mL
100 mM 0.0393 mL 0.1967 mL 0.3933 mL 0.7867 mL 0.9833 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 Alizarin 1-methyl ether

Anthraquinones from Hedyotis capitellata.[Pubmed:15924918]

Phytochemistry. 2005 May;66(10):1141-7.

Four new furanoanthraquinones, 2-hydroxymethyl-3,4-[2'-(1-hydroxy-1-methylethyl)-dihydrofurano]-8-hydroxyanthraq uinone, 2-hydroxymethyl-3,4-[1'-hydroxy-2'-(1-hydroxy-1-methylethyl)-dihydrofurano]-8-hyd roxyanthraquinone, 2-hydroxymethyl-3,4-[2'-1-hydroxy-1-methylethyl)-dihydrofurano]anthraquinone and 2-methyl-3,4-[2'-(1-hydroxy-1-methylethyl)-dihydrofurano] anthraquinone or capitellataquinone A-D and four known anthraquinones, rubiadin, anthragallol 2-methyl ether, Alizarin 1-methyl ether and digiferruginol, together with scopoletin were isolated from the stems of Hedyotis capitellata Wall (Rubiaceae). Lucidin-3-O-beta-glucoside was isolated from the roots of the plant. Characterization of the new compounds was carried out by extensive NMR studies using FGCOSY, FGHMQC, FGHMBC and DEPT-135 in addition to other spectroscopic methods.

Anthraquinones from the polar fractions of Galium sinaicum.[Pubmed:8688189]

Phytochemistry. 1996 Jul;42(4):1149-55.

The new anthraquinones, 6,7-dimethoxy xanthopurpurin, 6-hydroxy-7-methoxy rubiadin, 5-hydroxy-6-hydroxymethyl anthragallol 1, 3-dimethyl ether, 7-carboxy anthragallol 1,3-dimethyl ether, anthragallol 1-methyl ether 3-O-beta-D-glucopyranoside, anthragallol 1-methyl ether 3-O-rutinoside, anthragallol 3-O-rutinoside and Alizarin 1-methyl ether 2-O-primeveroside were isolated from the CH2Cl2 and n-BuOH extracts of Galium sinaicum roots and their structures were established by various spectroscopic techniques. In addition, two known anthraquinones were also isolated and fully characterized.

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