| Identification | Back Directory | [Name]
5-CARBOXYCYTOSINE | [CAS]
3650-93-9 | [Synonyms]
5-CARBOXYCYTOSINE
Uracil Impurity 8
Imidacloprid Impurity 30
cytosine-5-carboxylic acid
4-AMINO-5-CARBOXY-2-HYDROXYPYRIMIDINE
5-CARBOXYCYTOSINE ISO 9001：2015 REACH
4-AMINO-5-CARBOXY-2-HYDROXYPYRIMIDINE 97%
4-Amino-2-hydroxy-5-pyrimidinecarboxylicacid
6-amino-2-oxo-1H-pyrimidine-5-carboxylic acid
4-Amino-2-hydroxypyrimidine-5-carboxylic acid
6-azanyl-2-oxo-1H-pyrimidine-5-carboxylic acid
6-amino-2-keto-1H-pyrimidine-5-carboxylic acid
4-Amino-1,2-dihydro-2-oxo-5-pyrimidinecarboxylic acid
6-amino-1,2-dihydro-2-oxo-5-Pyrimidinecarboxylic acid
4-AMINO-2-OXO-1,2-DIHYDRO-PYRIMIDINE-5-CARBOXYLIC ACID
5-Pyrimidinecarboxylic acid, 6-amino-1,2-dihydro-2-oxo-
4-amino-2-hydroxypyrimidine-5-carboxylic acid hydrobromide
4-amino-2-hydroxy-5-pyrimidinecarboxylic acid(SALTDATA: FREE) | [EINECS(EC#)]
222-890-1 | [Molecular Formula]
C5H5N3O3 | [MDL Number]
MFCD00047368 | [MOL File]
3650-93-9.mol | [Molecular Weight]
155.11 |
| Chemical Properties | Back Directory | [Melting point ]
256-257 °C | [density ]
1.88±0.1 g/cm3(Predicted) | [storage temp. ]
Refrigerator, under inert atmosphere | [solubility ]
Aqueous Base (Slightly) | [form ]
Solid | [pka]
-3.50±0.20(Predicted) | [color ]
Pale Yellow to Pale Beige | [InChI]
1S/C5H5N3O3/c6-3-2(4(9)10)1-7-5(11)8-3/h1H,(H,9,10)(H3,6,7,8,11) | [InChIKey]
BLQMCTXZEMGOJM-UHFFFAOYSA-N | [SMILES]
NC1=NC(=O)NC=C1C(O)=O |
| Safety Data | Back Directory | [WGK Germany ]
WGK 3 | [HazardClass ]
IRRITANT | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Uses]
Cytosine derivatives, such as 5-Carboxylcytosine, are involved with a wide variety of biological functions including cytosine methylation, gene expression, genome stability, and chromatin modification. In addition, 5-Carboxylcytosine interacts with the RNA polymerase II elongation complex that can influence the pluripotent states during early embryonic development. | [Definition]
ChEBI: A nucleobase analogue that is cytosine in which the hydrogen at position 5 is replaced by a carboxy group. |
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| Company Name: |
Biokitchen
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| Tel: |
021-021-021-31663258 13795219287 |
| Website: |
www.chemicalbook.com/ShowSupplierProductsList20174/0_EN.htm |
| Company Name: |
Energy Chemical
|
| Tel: |
021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
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