8-HydroxythymolCAS# 4478-33-5 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
Cas No. | 4478-33-5 | SDF | Download SDF |
PubChem ID | N/A | Appearance | Oil |
Formula | C10H14O2 | M.Wt | 166.2 |
Type of Compound | Other Terpenoid | 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. |
8-Hydroxythymol Dilution Calculator
8-Hydroxythymol Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 6.0168 mL | 30.0842 mL | 60.1685 mL | 120.3369 mL | 150.4212 mL |
5 mM | 1.2034 mL | 6.0168 mL | 12.0337 mL | 24.0674 mL | 30.0842 mL |
10 mM | 0.6017 mL | 3.0084 mL | 6.0168 mL | 12.0337 mL | 15.0421 mL |
50 mM | 0.1203 mL | 0.6017 mL | 1.2034 mL | 2.4067 mL | 3.0084 mL |
100 mM | 0.0602 mL | 0.3008 mL | 0.6017 mL | 1.2034 mL | 1.5042 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. |
Calcutta University
University of Minnesota
University of Maryland School of Medicine
University of Illinois at Chicago
The Ohio State University
University of Zurich
Harvard University
Colorado State University
Auburn University
Yale University
Worcester Polytechnic Institute
Washington State University
Stanford University
University of Leipzig
Universidade da Beira Interior
The Institute of Cancer Research
Heidelberg University
University of Amsterdam
University of Auckland
TsingHua University
The University of Michigan
Miami University
DRURY University
Jilin University
Fudan University
Wuhan University
Sun Yat-sen University
Universite de Paris
Deemed University
Auckland University
The University of Tokyo
Korea University
- 2α,3α,24-Trihydroxyursa-12,20(30)-dien-28-oic acid
Catalog No.:BCN9347
CAS No.:341503-22-8
- Phochinenin I
Catalog No.:BCN9346
CAS No.:1070883-77-0
- Murrayafoline A
Catalog No.:BCN9345
CAS No.:4532-33-6
- Thymyl 2-methylbutyrate
Catalog No.:BCN9344
CAS No.:69844-32-2
- Methyl ganoderenate D
Catalog No.:BCN9343
CAS No.:748136-03-0
- Methyl lucidenate N
Catalog No.:BCN9342
CAS No.:1276655-49-2
- Cadambine
Catalog No.:BCN9341
CAS No.:54422-49-0
- 8,9-Dehydro-7,9-diisobutyryloxythymol
Catalog No.:BCN9340
CAS No.:22518-03-2
- Hancolupenone
Catalog No.:BCN9339
CAS No.:132746-04-4
- Phochinenin G
Catalog No.:BCN9338
CAS No.:1070883-75-8
- Jasnervoside C
Catalog No.:BCN9337
CAS No.:1622337-36-3
- 1-Methyleffusol
Catalog No.:BCN9336
CAS No.:144106-78-5
- Visartiside E
Catalog No.:BCN9349
CAS No.:1212005-08-7
- Girinimbine
Catalog No.:BCN9350
CAS No.:23095-44-5
- Benzyl [5-O-benzoyl-β-D-apiofuranosyl(1→2)]-β-D-glucopyranoside
Catalog No.:BCN9351
CAS No.:1097040-08-8
- Pomegralignan
Catalog No.:BCN9352
CAS No.:1562492-32-3
- Methyl lucidenate D
Catalog No.:BCN9353
CAS No.:98665-09-9
- 1-[2-Hydroxy-4-(hydroxymethyl)phenyl]ethanone
Catalog No.:BCN9354
CAS No.:22518-00-9
- Methyl lucidenate A
Catalog No.:BCN9355
CAS No.:105742-79-8
- 3-Hydroxyperillaldehyde
Catalog No.:BCN9356
CAS No.:1932348-11-2
- Convallagenin B
Catalog No.:BCN9357
CAS No.:17934-59-7
- Juncusol 2-O-glucoside
Catalog No.:BCN9358
CAS No.:175094-14-1
- Betulinic acid palmitate
Catalog No.:BCN9359
CAS No.:19833-15-9
- 6,6'-Di-O-sinapoylsucrose
Catalog No.:BCN9360
CAS No.:1068661-35-7
New thymol derivatives and cytotoxic constituents from the root of Eupatorium cannabinum ssp. asiaticum.[Pubmed:25238078]
Chem Biodivers. 2014 Sep;11(9):1374-80.
Two new thymol (=5-methyl-2-(1-methylethyl)phenol) derivatives, 8,10-didehydro-9-(3-methylbutanoyl)thymol 3-O-tiglate (1) and 9-O-angeloyl-8-methoxythymol 3-O-isobutyrate (2), were isolated from the root of Eupatorium cannabinum ssp. asiaticum, together with six known compounds, 3-8. The structures of 1 and 2 were determined through extensive 1D/2D-NMR and MS analyses. Among the isolates, 9-acetoxy-8,10-epoxythymol 3-O-tiglate (3) was the most cytotoxic, with IC50 values of 0.02+/-0.01, 1.02+/-0.07, and 1.36+/-0.12 mug/ml, respectively, against DLD-1, CCRF-CEM, and HL-60 cell lines. In addition, 10-acetoxy-9-O-angeloyl-8-Hydroxythymol (4) and eupatobenzofuran (6) exhibited cytotoxicities, with IC50 values of 1.14+/-0.16 and 2.63+/-0.22, and 7.63+/-0.94 and 2.31+/-0.14 mug/ml, respectively, against DLD-1 and CCRF-CEM cell lines.
New 2,2-diphenylpropane and ethoxylated aromatic monoterpenes from Lavandula gibsoni (Lamiaceae).[Pubmed:23126635]
Nat Prod Res. 2013 Aug;27(15):1323-9.
A new substituted 2,2-diphenylpropane (1) and two new ethoxylated aromatic monoterpene alcohols (2 and 4) have been isolated from the acetone extract of the aerial parts of Lavandula gibsoni, along with the known compounds 8-hydroxycarvacrol (3), 8-Hydroxythymol (5), coumarin (6), 4-methylresorcinol (7), 7,4'-dimethylapigenin (8), salvigenin (9), beta-sitosteryl-3-O-beta-D-glucopyranosyl-6'-O-palmitate (10) and euscaphic acid D (11). The structures of the isolated compounds were assigned on the basis of their (1)H- and (13)C-NMR spectra and two-dimensional NMR techniques, which included COSY, HSQC, HMBC and NOESY experiments and comparison with the reported literature.