ResorcinolCAS# 108-46-3 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 108-46-3 | SDF | Download SDF |
| PubChem ID | 5054 | Appearance | White powder |
| Formula | C6H6O2 | M.Wt | 110.1 |
| Type of Compound | Phenols | Storage | Desiccate at -20°C |
| Synonyms | Resorcin; 1,3-Benzenediol | ||
| Solubility | Freely soluble in ethanol and water; sparingly soluble in chloroform | ||
| Chemical Name | benzene-1,3-diol | ||
| SMILES | C1=CC(=CC(=C1)O)O | ||
| Standard InChIKey | GHMLBKRAJCXXBS-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C6H6O2/c7-5-2-1-3-6(8)4-5/h1-4,7-8H | ||
| 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. |
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| 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. |
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| 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. | ||
| Description | Resorcinol is an antiseptic and a disinfectant, and a chemical intermediate for the production of many other pharmaceuticals，is used to treat acne, seborrheic dermatitis, eczema, psoriasis, and other skin disorders. |
| In vivo | Resorcinol peels as a possible self-treatment of painful nodules in hidradenitis suppurativa.[Pubmed: 19549239 ]Clin Exp Dermatol. 2010 Jan;35(1):36-40.
Hidradenitis suppurativa (HS) is a chronic, inflammatory skin disease characterized by abscess formation localized to apocrine sweat gland-bearing skin. The most important factor in patients' overall assessment of disease severity is pain. The duration of abscesses takes days to weeks and are always painful. AIM: To assess the efficacy of self-treatment with topical 15% Resorcinol in an open study.
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| Structure Identification | Phys Chem Chem Phys. 2015 Feb 4;17(7):5236-47.Structural investigation of resorcinol based symmetrical banana mesogens by XRD, NMR and polarization measurements.[Pubmed: 25603887]Synthesis and structural characterization of two novel symmetrical banana mesogens built from Resorcinol with seven phenyl rings linked by ester and imine with a terminal dodecyl/dodecyloxy chain has been carried out. Density functional theory (DFT) has been employed for obtaining the geometry optimized structures, the dipole moments and (13)C NMR chemical shifts. The HOPM and DSC studies revealed enantiotropic B2 and B7 phases for the dodecyl and dodecyloxy homologs respectively. The powder X-ray studies of both the mesogens indicate the presence of layer ordering. The polarization measurements reveal an anti-ferroelectric switching for the B2 phase of the dodecyl homolog whose structure has been identified as SmCSPA. The B7 phase of the dodecyloxy homolog was found to be non-switchable. High resolution (13)C NMR study of the dodecyl homolog in its mesophase has been carried out. (13)C-(1)H dipolar couplings obtained from the 2-dimensional separated local field spectroscopy experiment were used to obtain the orientational order parameters of the different segments of the mesogen. Very large (13)C-(1)H dipolar couplings observed for the carbons of the central phenyl ring (9.7-12.3 kHz) in comparison to the dipolar couplings of those of the side arm phenyl rings (less than 3 kHz) are a direct consequence of the ordering in the banana phase and the shape of the molecule. From the ratio of the local order parameter values, the bent-angle of the mesogen could be determined in a straight forward manner to be 120.5°. |
Resorcinol Dilution Calculator
Resorcinol Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 9.0827 mL | 45.4133 mL | 90.8265 mL | 181.653 mL | 227.0663 mL |
| 5 mM | 1.8165 mL | 9.0827 mL | 18.1653 mL | 36.3306 mL | 45.4133 mL |
| 10 mM | 0.9083 mL | 4.5413 mL | 9.0827 mL | 18.1653 mL | 22.7066 mL |
| 50 mM | 0.1817 mL | 0.9083 mL | 1.8165 mL | 3.6331 mL | 4.5413 mL |
| 100 mM | 0.0908 mL | 0.4541 mL | 0.9083 mL | 1.8165 mL | 2.2707 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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Resorcinol is an antiseptic and a disinfectant, and a chemical intermediate for the production of many other pharmaceuticals，is used to treat acne, seborrheic dermatitis, eczema, psoriasis, and other skin disorders.
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Structural investigation of resorcinol based symmetrical banana mesogens by XRD, NMR and polarization measurements.[Pubmed:25603887]
Phys Chem Chem Phys. 2015 Feb 21;17(7):5236-47.
Synthesis and structural characterization of two novel symmetrical banana mesogens built from Resorcinol with seven phenyl rings linked by ester and imine with a terminal dodecyl/dodecyloxy chain has been carried out. Density functional theory (DFT) has been employed for obtaining the geometry optimized structures, the dipole moments and (13)C NMR chemical shifts. The HOPM and DSC studies revealed enantiotropic B2 and B7 phases for the dodecyl and dodecyloxy homologs respectively. The powder X-ray studies of both the mesogens indicate the presence of layer ordering. The polarization measurements reveal an anti-ferroelectric switching for the B2 phase of the dodecyl homolog whose structure has been identified as SmCSPA. The B7 phase of the dodecyloxy homolog was found to be non-switchable. High resolution (13)C NMR study of the dodecyl homolog in its mesophase has been carried out. (13)C-(1)H dipolar couplings obtained from the 2-dimensional separated local field spectroscopy experiment were used to obtain the orientational order parameters of the different segments of the mesogen. Very large (13)C-(1)H dipolar couplings observed for the carbons of the central phenyl ring (9.7-12.3 kHz) in comparison to the dipolar couplings of those of the side arm phenyl rings (less than 3 kHz) are a direct consequence of the ordering in the banana phase and the shape of the molecule. From the ratio of the local order parameter values, the bent-angle of the mesogen could be determined in a straight forward manner to be 120.5 degrees .
