Structure
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Cytidine

Structure
Product Name
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;Cytosine β-D-riboside;Citidine;Cytidin;Cytidine;Cytinide;Cytidylic
CBNumber
CB7854079
Molecular Formula
C9H13N3O5
Formula Weight
243.22
MOL File
65-46-3.mol
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Cytidine Property

Melting point:
210-220 °C (dec.) (lit.)
alpha 
31.5 º (c=0.6, H2O 25 ºC)
Boiling point:
386.09°C (rough estimate)
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
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.
LogP
-1.808 (est)
CAS DataBase Reference
65-46-3(CAS DataBase Reference)
NIST Chemistry Reference
Cytidine(65-46-3)
EPA Substance Registry System
Cytidine (65-46-3)
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Safety

Risk Statements 
68
Safety Statements 
24/25
WGK Germany 
3
RTECS 
UW7370000
10-23
TSCA 
Yes
HS Code 
29349990
Toxicity
LD50 intraperitoneal in mouse: 2700mg/kg
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
C122106
Product name
Cytidine
Purity
99%
Packaging
1g
Price
$27.2
Updated
2024/03/01
Sigma-Aldrich
Product number
C122106
Product name
Cytidine
Purity
99%
Packaging
10g
Price
$74
Updated
2024/03/01
TCI Chemical
Product number
C0522
Product name
Cytidine
Purity
>98.0%(HPLC)(T)
Packaging
1g
Price
$27
Updated
2024/03/01
TCI Chemical
Product number
C0522
Product name
Cytidine
Purity
>98.0%(HPLC)(T)
Packaging
5g
Price
$49
Updated
2024/03/01
Alfa Aesar
Product number
A10261
Product name
Cytidine, 99%
Packaging
10g
Price
$59.65
Updated
2024/03/01
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Cytidine Chemical Properties,Usage,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.

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.

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.

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.]

Cytidine Preparation Products And Raw materials

Raw materials

Preparation Products

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Cytidine Suppliers

INTATRADE GmbH
Tel
+49 3493/605464
Fax
+49 3493/605470
Email
sales@intatrade.de
Country
Germany
ProdList
3572
Advantage
66
Pharma Waldhof Gmbh
Tel
--
Fax
--
Email
info@pharmawaldhof.de
Country
Germany
ProdList
67
Advantage
58
Burmester Pharmatrade Gmbh
Tel
--
Fax
--
Email
info@burmester-pharma.de
Country
Germany
ProdList
1347
Advantage
58
Alfa Aesar, Thermo Fisher Scientific
Tel
--
Fax
--
Email
es@alfa.com
Country
Germany
ProdList
5123
Advantage
58
CHEMOS GmbH & Co. KG
Tel
--
Fax
--
Email
chemos@chemos.de
Country
Germany
ProdList
6727
Advantage
58
ABCR GmbH & CO. KG
Tel
--
Fax
--
Email
info@abcr.de
Country
Germany
ProdList
6831
Advantage
75
PARAGOS
Tel
--
Fax
--
Email
info@paragos.com
Country
Germany
ProdList
6371
Advantage
39
chemcube
Tel
--
Fax
--
Email
sales@chemcube.eu
Country
Germany
ProdList
4083
Advantage
34
Service Chemical Inc.
Tel
--
Fax
--
Email
sales@chemos-group.com
Country
Germany
ProdList
6350
Advantage
71
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View Lastest Price from Cytidine manufacturers

HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
Product
Cytidine 65-46-3
Price
US $999.00-800.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
5000
Release date
2024-08-21
WUHAN FORTUNA CHEMICAL CO., LTD
Product
Cytidine 65-46-3
Price
US $0.00/Kg/Drum
Min. Order
1KG
Purity
99%min HPLC
Supply Ability
1000KGS
Release date
2021-08-06
Hebei Zhuanglai Chemical Trading Co Ltd
Product
Cytidine 65-46-3
Price
US $55.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20 tons
Release date
2024-11-21

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