4-Amino-N-methylphthalimideCAS# 2307-00-8 |
2D Structure
Quality Control & MSDS
3D structure
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Number of papers citing our products
Cas No. | 2307-00-8 | SDF | Download SDF |
PubChem ID | 726931 | Appearance | Powder |
Formula | C9H8N2O2 | M.Wt | 176 |
Type of Compound | N/A | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | 5-amino-2-methylisoindole-1,3-dione | ||
SMILES | CN1C(=O)C2=C(C1=O)C=C(C=C2)N | ||
Standard InChIKey | KMEBUNSLFRQSEM-UHFFFAOYSA-N | ||
Standard InChI | InChI=1S/C9H8N2O2/c1-11-8(12)6-3-2-5(10)4-7(6)9(11)13/h2-4H,10H2,1H3 | ||
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. |
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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. |
4-Amino-N-methylphthalimide Dilution Calculator
4-Amino-N-methylphthalimide Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 5.6818 mL | 28.4091 mL | 56.8182 mL | 113.6364 mL | 142.0455 mL |
5 mM | 1.1364 mL | 5.6818 mL | 11.3636 mL | 22.7273 mL | 28.4091 mL |
10 mM | 0.5682 mL | 2.8409 mL | 5.6818 mL | 11.3636 mL | 14.2045 mL |
50 mM | 0.1136 mL | 0.5682 mL | 1.1364 mL | 2.2727 mL | 2.8409 mL |
100 mM | 0.0568 mL | 0.2841 mL | 0.5682 mL | 1.1364 mL | 1.4205 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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Response characterization of a fiber optic sensor array with dye-coated planar waveguide for detection of volatile organic compounds.[Pubmed:24988381]
Sensors (Basel). 2014 Jul 1;14(7):11659-71.
We have developed a multi-array side-polished optical-fiber gas sensor for the detection of volatile organic compound (VOC) gases. The side-polished optical-fiber coupled with a polymer planar waveguide (PWG) provides high sensitivity to alterations in refractive index. The PWG was fabricated by coating a solvatochromic dye with poly(vinylpyrrolidone). To confirm the effectiveness of the sensor, five different sensing membranes were fabricated by coating the side-polished optical-fiber using the solvatochromic dyes Reinhardt's dye, Nile red, 4-aminophthalimide, 4-Amino-N-methylphthalimide, and 4-(dimethylamino)cinnamaldehyde, which have different polarities that cause changes in the effective refractive index of the sensing membrane owing to evanescent field coupling. The fabricated gas detection system was tested with five types of VOC gases, namely acetic acid, benzene, dimethylamine, ethanol, and toluene at concentrations of 1, 2,...,10 ppb. Second-regression and principal component analyses showed that the response properties of the proposed VOC gas sensor were linearly shifted bathochromically, and each gas showed different response characteristics.
Ultrashort-lived excited states of aminophthalimides in fluid solution.[Pubmed:12803081]
Photochem Photobiol Sci. 2003 May;2(5):576-84.
The Sn-->S0 ultraviolet fluorescence spectra (270-380 nm) of 4-aminophthalimide (4AP) and its N-methyl derivative 4-Amino-N-methylphthalimide (4ANMP) are reported, following the absorption of two laser pulses. In polar but non-hydrogen-bonding solvents, both molecules exhibit a principal emission maximum near 290 nm, whereas solutions in hydrogen-bonding solvents display two prominent emission bands, near 300 and 350 nm. The relative intensities of these bands depend on solvent type and, in a pump-probe experiment, on the wavelengths and temporal spacing of two ultrashort pulses. Experiments covering the range approximately 0.1-100 ps showed evidence for at least two distinct ultrashort relaxation processes, the rates of which depend on solvent. Fluorescence upconversion experiments at < 0.2 ps resolution have shown that the longer-duration process correlates with the fluorescence Stokes shift, and provide evidence that the solvent-dependent shift of the S1-->S0 fluorescence spectrum is reflected in the fluorescence quantum efficiency of a nearby electronic state.