Cytidine 5′-triphosphate disodium salt - 10mM in Water , CAS No.36051-68-0

CAS: 36051-68-0 Cat. No.: C423622 Molecular Weight: 527.12 EC Number: 252-849-3 PubChem CID: 16219084
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GRADE & PURITY 10mM in Water
Synonyms
36051-68-0|Cytidine-5'-triphosphate disodium salt|Cytidine 5'-triphosphate disodium salt|Cytidine-5'-triphosphoric acid disodium salt|disodium;[[[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl]oxy-hydroxypho
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Status
Price
Qty
1ml
C423622-1ml
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Why this grade

10mM in Water for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 29 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Cytidine 5′-triphosphate is a nucleoside triphosphate with a pyrimidine ring. It is present in RNA

Cytidine 5′-triphosphate disodium salt has been used:

• for the conversion of adenosine monophosphate (AMP) to adenosine diphosphate (ADP) in luminometry analysis

• in the preparation of ribonucleotide 5′-triphosphate precursors stocks for large-scale RNA synthesis

• to perform in vitro transcription

Specifications

Synonyms
36051-68-0 | Cytidine-5'-triphosphate disodium salt | Cytidine 5'-triphosphate disodium salt | Cytidine-5'-triphosphoric acid disodium salt | disodium;[[[(2R, 3S, 4R, 5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3, 4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl]oxy-hydroxypho
Specifications & Purity
10mM in Water
Biochemical and Physiological Mechanisms
Pyrimidine nucleoside triphosphate involved in a variety of biochemical reactions. Used in the synthesis of RNA by RNA polymerases. Used as a substrate for CMP-neuNAc synthetase(s) which produce CMP-neuNAc used in sialylation reactions.
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers
Canonical SmilesC1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OP(=O)(O)[O-])O)O.[Na+].[Na+]
IUPAC Namedisodium;[[[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-oxidophosphoryl]oxy-hydroxyphosphoryl] hydrogen phosphate
InChIKeyNFQMDTRPCFJJND-WFIJOQBCSA-L
INCHI1S/C9H16N3O14P3.2Na/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(24-8)3-23-28(19,20)26-29(21,22)25-27(16,17)18;;/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H,21,22)(H2,10,11,15)(H2,16,17,18);;/q;2*+1/p-2/t4-,6-,7-,8-;;/m1../s1
Isomeric SMILES C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)([O-])OP(=O)(O)OP(=O)(O)[O-])O)O.[Na+].[Na+]
WGK Germany 3
Alternate CAS 123334-07-6
PubChem CID 16219084
Molecular Weight 527.12

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassNucleosides, nucleotides, and analogues
ClassPyrimidine nucleotides
SubclassPyrimidine ribonucleotides
Intermediate Tree Nodes Not available
Direct ParentPyrimidine ribonucleoside triphosphates
Alternative Parents Pentose phosphates  Glycosylamines  Monosaccharide phosphates  Aminopyrimidines and derivatives  Pyrimidones  Monoalkyl phosphates  Hydropyrimidines  Imidolactams  Heteroaromatic compounds  Oxolanes  Secondary alcohols  1,2-diols  Oxacyclic compounds  Azacyclic compounds  Organic zwitterions  Hydrocarbon derivatives  Primary amines  Organic sodium salts  Organic oxides  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Pyrimidine ribonucleoside triphosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Pentose monosaccharide - Aminopyrimidine - Pyrimidone - Monoalkyl phosphate - Hydropyrimidine - Monosaccharide - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Imidolactam - Oxolane - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Organic alkali metal salt - Oxacycle - Azacycle - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organic salt - Organic sodium salt - Organic oxygen compound - Primary amine - Organic nitrogen compound - Organic zwitterion - Organic oxide - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as pyrimidine ribonucleoside triphosphates. These are pyrimidine ribobucleotides with triphosphate group linked to the ribose moiety.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
Flash Point(°F)235.4 °F
Flash Point(°C)113 °C
Citations of This Product
References
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