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About This Item
Empirical Formula (Hill Notation):
C9H13N3O5
CAS Number:
Molecular Weight:
243.22
UNSPSC Code:
41106305
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-610-9
Beilstein/REAXYS Number:
89173
MDL number:
Assay:
99%
Form:
powder
Storage temp.:
2-8°C
Quality Level
assay
99%
form
powder
optical activity
[α]20/D +33°, c = 2 in H2O
mp
210-220 °C (dec.) (lit.)
storage temp.
2-8°C
SMILES string
NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O
InChI
1S/C9H13N3O5/c10-5-1-2-12(9(16)11-5)8-7(15)6(14)4(3-13)17-8/h1-2,4,6-8,13-15H,3H2,(H2,10,11,16)/t4-,6-,7-,8-/m1/s1
InChI key
UHDGCWIWMRVCDJ-XVFCMESISA-N
Gene Information
mouse ... Uck1(22245)
General description
Cytidine also known as cytosine β-D-riboside, is a nucleoside, commonly used in organic synthesis.
Application
Cytidine can be used as a building block to synthesize 5‘-hydroxy-5‘-phosphonate derivatives of cytidine. Additionally, it is used to regulate the phosphatidate phosphatase activity by nucleotides.
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Regulation of phosphatidate phosphatase activity from the yeast Saccharomyces cerevisiae by nucleotides.
The Journal of Biological Chemistry, 269, 29495-29501 (1994)
Stereoselective synthesis of the 5 `-hydroxy-5 `-phosphonate derivatives of cytidine and cytosine arabinoside
X Chen
The Journal of Organic Chemistry, 67, 9331-9339 (2002)
G P Gerrits et al.
Clinical chemistry, 34(7), 1439-1442 (1988-07-01)
Disturbances in the metabolism of purines and pyrimidines in neurologically affected patients can be reflected by aberrant concentrations of nucleosides and nucleobases in cerebrospinal fluid (CSF). However, normal values, especially for children at different ages, are lacking. We collected 1000