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Merck
CN

M5634

5-Mercuricytidine carbonate 5′-triphosphate triethylammonium salt

~90%

Synonym(s):

Hg-CTP

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About This Item

Linear Formula:
C9H15HgN3O14P3 · HCO3
CAS Number:
100940-62-3
Molecular Weight:
1148.52
NACRES:
NA.51
PubChem Substance ID:
329818019
UNSPSC Code:
41106305
MDL number:
MFCD00058366
Assay:
~90%
Form:
solid
Storage temp.:
−20°C

Key Documents

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InChI

1S/C9H15N3O14P3.C6H15N.Hg/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;1-4-7(5-2)6-3;/h2,4,6-8,13-14H,3H2,(H,19,20)(H,21,22)(H2,10,11,15)(H2,16,17,18);4-6H2,1-3H3;/t4-,6-,7-,8-;;/m1../s1

SMILES string

CCN(CC)CC.NC1=NC(=O)N(C=C1[Hg])[C@@H]2O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]2O

InChI key

CKMVNPSLWQKVPG-WFIJOQBCSA-N

assay

~90%

form

solid

storage temp.

−20°C

Application

5-Mercuricytidine carbonate 5;-triphosphate (Hg-CTP) may be used as a substrate to generate mercurated DNA that may be suitable for image based DNA sequencing strategies.

Disclaimer

For U.S. Customers: Contains mercury; Do not place in trash - dispose according to local, state, or federal laws.

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Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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A J Bridgman et al.
DNA sequence : the journal of DNA sequencing and mapping, 6(4), 199-209 (1996-01-01)
The development of high-resolution scanning-probe microscopes has reawakened interest in the possibility of sequencing large nucleic acid molecules by direct imaging. Such an approach would be facilitated by the availability of effective methods for increasing contrast by labelling specific nucleotides
G Banfalvi et al.
Analytical biochemistry, 146(1), 64-70 (1985-04-01)
A method for isolating picomole quantities of nascent mercurated DNA from a mixture of cellular nucleic acids using affinity chromatography on thiol-agarose is described. Analysis of mercurated DNA (HgDNA) isolated in the presence of in vivo-labeled cellular RNA or in
Study of deoxyribonucleic acid replication in permeable cells of Bacillus subtilis using mercurated nucleotide substrates.
S Bhattacharya et al.
Biochemistry, 20(11), 3029-3034 (1981-05-26)
Structural analyses on the mercury(II)-mediated T-T base pair.
Tanaka Y, Oda S, et al.
Nucleic Acids Symposium Series, 50, 47-48 (2006)
R M Dale et al.
Proceedings of the National Academy of Sciences of the United States of America, 70(8), 2238-2242 (1973-08-01)
A simple acetoxymercuration reaction for introducing covalently bound mercury atoms into nucleotides is described. The 5-mercuriacetate derivatives of UTP, CTP, dUTP, and dCTP, as well as the 7-mercuriacetate derivative of 7-deazaATP, have been prepared by this procedure and tested as
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