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6-Aminouracil

CAS# 873-83-6

6-Aminouracil

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6-Aminouracil: 5mg $17 In Stock
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Chemical structure

6-Aminouracil

3D structure

Chemical Properties of 6-Aminouracil

Cas No. 873-83-6 SDF Download SDF
PubChem ID 70120 Appearance Powder
Formula C4H5N3O2 M.Wt 127
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 6-amino-1H-pyrimidine-2,4-dione
SMILES C1=C(NC(=O)NC1=O)N
Standard InChIKey LNDZXOWGUAIUBG-UHFFFAOYSA-N
Standard InChI InChI=1S/C4H5N3O2/c5-2-1-3(8)7-4(9)6-2/h1H,(H4,5,6,7,8,9)
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.

6-Aminouracil Dilution Calculator

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6-Aminouracil Molarity Calculator

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Preparing Stock Solutions of 6-Aminouracil

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 7.874 mL 39.3701 mL 78.7402 mL 157.4803 mL 196.8504 mL
5 mM 1.5748 mL 7.874 mL 15.748 mL 31.4961 mL 39.3701 mL
10 mM 0.7874 mL 3.937 mL 7.874 mL 15.748 mL 19.685 mL
50 mM 0.1575 mL 0.7874 mL 1.5748 mL 3.1496 mL 3.937 mL
100 mM 0.0787 mL 0.3937 mL 0.7874 mL 1.5748 mL 1.9685 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 6-Aminouracil

Chromophoric Nucleoside Analogues: Synthesis and Characterization of 6-Aminouracil-Based Nucleodyes.[Pubmed:27128151]

J Org Chem. 2016 Jun 3;81(11):4530-9.

Nucleodyes, visibly colored chromophoric nucleoside analogues, are reported. Design criteria are outlined and the syntheses of cytidine and uridine azo dye analogues derived from 6-Aminouracil are described. Structural analysis shows that the nucleodyes are sound structural analogues of their native nucleoside counterparts, and photophysical studies demonstrate that the nucleodyes are sensitive to microenvironmental changes. Quantum chemical calculations are presented as a valuable complementary tool for the design of strongly absorbing nucleodyes, which overlap with the emission of known fluorophores. Forster critical distance (R0) calculations determine that the nucleodyes make good FRET pairs with both 2-aminopurine (2AP) and pyrrolocytosine (PyC). Additionally, unique tautomerization features exhibited by 5-(4-nitrophenylazo)-6-oxocytidine (8) are visualized by an extraordinary crystal structure.

Three new pseudopolymorphs of 6-aminouracil.[Pubmed:24192197]

Acta Crystallogr C. 2013 Nov;69(Pt 11):1402-7.

Since 6-Aminouracil derivatives show diversified use in various fields of application, we crystallized 6-Aminouracil to examine its preferred hydrogen-bonding frameworks. 6-Aminouracil shows two rigid hydrogen-bonding sites, viz. one acceptor-donor-acceptor (ADA) site and one donor-donor-acceptor (DDA) site. During various crystallization attempts, we obtained three structures, namely two dimethylacetamide monosolvates, C4H5N3O2.C4H9NO, and a 1-methylpyrrolidin-2-one monosolvate, C4H5N3O2.C5H9NO. In all three structures, R2(1)(6) N-H...O hydrogen-bonding patterns link the molecules to their respective solvent molecules. The formation of R2(2)(8) N-H...O hydrogen-bond motifs between 6-Aminouracil molecules can only be found in two-dimensional frameworks, whereas R3(3)(14) N-H...O patterns are present when zigzag chzins of 6-Aminouracil molecules are formed.

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