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Cytidine

CAS No.
65-46-3
Chemical Name:
Cytidine
Synonyms
4-aMino-1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxyMethyl)tetrahydrofuran-2-yl)pyriMidin-2(1H)-one;Cyd;Citydine;Cytosine β-D-riboside;Citidine;Cytidin;Cytidine;Cytinide;Cytidylic;Cytidine >
CBNumber:
CB7854079
Molecular Formula:
C9H13N3O5
Molecular Weight:
243.22
MDL Number:
MFCD00006545
MOL File:
65-46-3.mol
MSDS File:
SDS
Last updated:2026-02-02 18:10:39
Product description Number Pack Size Price
Cytidine certified reference material, pharmaceutical secondary standard PHR3802 100mg $616
Cytidine 99% C122106 1g $28
Cytidine 99% C122106 10g $76.3
Cytidine >98.0%(HPLC)(T) C0522 1g $27
Cytidine >98.0%(HPLC)(T) C0522 5g $49
More product size

Cytidine Properties

Melting point 210-220 °C (dec.) (lit.)
Boiling point 386.09°C (rough estimate)
alpha 31.5 º (c=0.6, H2O 25 ºC)
Density 1.3686 (rough estimate)
refractive index 34 ° (C=0.7, H2O)
storage temp. 2-8°C
solubility H2O: 50 mg/mL
form powder
pka 4.22, 12.5(at 25℃)
color White to almost white
PH 4.13
biological source synthetic
optical activity [α]20/D +33°, c = 2 in H2O
Water Solubility SOLUBLE
Sensitive Hygroscopic
λmax 280 (pH 1);229.5,271 (pH 7)
Merck 14,2786
BRN 89173
Stability Stable. Incompatible with strong oxidizing agents. Protect from moisture.
Cosmetics Ingredients Functions SKIN PROTECTING
SKIN CONDITIONING
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
InChIKey UHDGCWIWMRVCDJ-XVFCMESISA-N
SMILES NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O
LogP -1.808 (est)
CAS DataBase Reference 65-46-3(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 5CSZ8459RP
NIST Chemistry Reference Cytidine(65-46-3)
EPA Substance Registry System Cytidine (65-46-3)
UNSPSC Code 41116107
NACRES NA.75

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338
PPE Eyeshields, Gloves, type N95 (US)
Risk Statements  68
Safety Statements  24/25
WGK Germany  3
RTECS  UW7370000
10-23
TSCA  TSCA listed
HS Code  29349990
Storage Class 11 - Combustible Solids
Toxicity LD50 intraperitoneal in mouse: 2700mg/kg
NFPA 704
1
0 1

Cytidine price More Price(62)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHR3802 Cytidine certified reference material, pharmaceutical secondary standard 65-46-3 100mg $616 2025-07-31 Buy
Sigma-Aldrich C122106 Cytidine 99% 65-46-3 1g $28 2025-07-31 Buy
Sigma-Aldrich C122106 Cytidine 99% 65-46-3 10g $76.3 2025-07-31 Buy
TCI Chemical C0522 Cytidine >98.0%(HPLC)(T) 65-46-3 1g $27 2025-07-31 Buy
TCI Chemical C0522 Cytidine >98.0%(HPLC)(T) 65-46-3 5g $49 2025-07-31 Buy
Product number Packaging Price Buy
PHR3802 100mg $616 Buy
C122106 1g $28 Buy
C122106 10g $76.3 Buy
C0522 1g $27 Buy
C0522 5g $49 Buy

Cytidine Chemical Properties,Uses,Production

Structure

The crystal specimens were kindly supplied by Dr. D. O. Jordan, University of Nottingham, and were found to be orthorhombic with {110} dominating. An optical investigation shows that the sign is positive, with α∥c, β∥b and γ∥a. Cell dimensions are: a = 13·93 A., b = 14·75 A., c = 5·10 A.; density, 1·53; four molecules per unit cell; space-group, P 212121.

Description

Cytidine is a pyrimidine nucleoside that is composed of the pyrimidine base cytosine attached to the sugar ribose. As a constituent of RNA, cytidine pairs with guanine, and it is a precursor of uridine. Cytidine can incur several modifications in mRNA, including methylation and acetylation, that function to regulate translation. Cytidine can also be formylated to 5-formylcytidine in mitochondrial methionine transfer RNA (tRNAMet).

Chemical Properties

Cytidine is a component of RNA. It is a white water-soluble solid. which is only slightly soluble in ethanol.There are a variety of cytidine analogs with potentially useful pharmacology.

Uses

Cytidine is a nucleoside molecule that is formed when cytosine is attached to a ribose ring, cytidine is a component of RNA. It was isolated from yeast nucleic acid. It can increases cell membrane phospholipids. Cytidine is used to synthesize enzyme inhibitors, antiviral agents, and anticancer agents. And also used as constituent of nucleic acids.

Application

Cytidine has been used as a non-essential aminoacid component of minimal essential medium (MEM) to analyse interspecies somatic cell nucleus transfer (iSCNT)-derived blastocysts. It has also been used as a supplement in the culture medium of HeLa cells, to study the effects of cytidine addition on rods and rings (RR) induced by glutamine deprivation.
Cytidine has been used as a component to prepare ribonucleoside stock solution to assess its effects on the anaerobic growth of several Bacillus mojavensis strains.

Definition

ChEBI: cytidine is a pyrimidine nucleoside in which cytosine is attached to ribofuranose via a beta-N(1)-glycosidic bond. It has a role as a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. It derives from a cytosine.The derivednucleotides, cytidine mono-, di-, andtriphosphate (CMP, CDP, and CTP respectively)participate in various biochemicalreactions, notably inphospholipid synthesis.

General Description

White crystalline powder.

Air & Water Reactions

Cytidine is hygroscopic. Water soluble.

Reactivity Profile

Cytidine is incompatible with strong oxidizing agents. . Will react as a weak base.

Fire Hazard

Flash point data for Cytidine are not available; however, Cytidine is probably combustible.

Purification Methods

Cytidine crystallises from 90% aqueous EtOH. It has also been converted to sulfate by dissolving (~200mg) in a solution of EtOH (10mL) containing H2SO4 (50mg), whereby the salt crystallises out. It is collected, washed with EtOH and dried for 5hours at 120o/0.1mm. The sulfate has m 225o. The free base is obtained by shaking the salt solution with a weak ion-exchange resin, filtering, evaporating and recrystallising the residue from EtOH as before. [Fox & Goodman J Am Chem Soc 73 3256 1956, Fox & Shugar Biochim Biophys Acta 9 369 1952; see Prytsas & Sorm in Synthetic Procedures in Nucleic Acid Chemistry (Zorbach & Tipson Eds) Vol 1 404 1973.] [Beilstein 25 III/IV 3667.]

References

[1] Nucleotide Biosynthesis Process[J]. Definitions, 2020, 30 1. DOI: 10.32388/28chil
[2] EMMANUEL MARTIN. CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferation[J]. Nature, 2014, 510 7504: 288-292. DOI: 10.1038/nature13386

36468-53-8
71-30-7
65-46-3
Synthesis of Cytidine from beta-D-Ribofuranose (9CI) and Cytosine
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View Lastest Price from Cytidine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Cytidine pictures 2026-02-24 Cytidine
65-46-3
0.99 RongNa Biotechnology Co.,Ltd
Cytidine pictures 2026-02-24 Cytidine
65-46-3
US $0.00-0.00 / kg 1kg ≥99% 20 tons Hangzhou Meiya Pharmaceutical Co Ltd
Cytidine pictures 2026-02-24 Cytidine
65-46-3
US $999.00-800.00 / kg 1kg 99% 5000 HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
  • Cytidine pictures
  • Cytidine
    65-46-3
  • 0.99
  • RongNa Biotechnology Co.,Ltd
  • Cytidine pictures
  • Cytidine
    65-46-3
  • US $0.00-0.00 / kg
  • ≥99%
  • Hangzhou Meiya Pharmaceutical Co Ltd
  • Cytidine pictures
  • Cytidine
    65-46-3
  • US $999.00-800.00 / kg
  • 99%
  • HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
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