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2′-Deoxyguanosine 5′-triphosphate trisodium salt - 98%, high purity , CAS No.93919-41-6

    Grade & Purity:
  • ≥98%
In stock
Item Number
D112856
Grouped product items
SKU Size
Availability
Price Qty
D112856-50mg
50mg
3
$98.90
D112856-250mg
250mg
3
$445.90
D112856-1g
1g
2
$1,603.90

Purine nucleoside triphosphate.

Basic Description

Synonyms dGTP-Na3 | sodium ((2R,3S,5R)-5-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)-3-hydroxytetrahydrofuran-2-yl)methyl hydrogen triphosphate | 2'-Deoxyguanosine 5'-triphosphate trisodium salt Solution | trisodium;[[[(2R,3S,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3-hy
Specifications & Purity ≥98%
Biochemical and Physiological Mechanisms It is used in vivo synthesis for the synthesis of DNA via DNA polymerases.Purine nucleoside triphosphate used in many molecular biology applications such as DNA sequencing, PCR and other DNA polymerase based DNA synthesis and repair techniques. Used in vi
Storage Temp Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Note Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

2′-Deoxyguanosine 5′-triphosphate trisodium salt is utilized for methods such as DNA sequencing, PCR and other DNA polymerase based DNA synthesis and repair techniques.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Nucleosides, nucleotides, and analogues
Class Purine nucleotides
Subclass Purine deoxyribonucleotides
Intermediate Tree Nodes Purine deoxyribonucleoside triphosphates
Direct Parent Purine 2'-deoxyribonucleoside triphosphates
Alternative Parents Hypoxanthines  6-oxopurines  Pyrimidones  Aminopyrimidines and derivatives  N-substituted imidazoles  Alkyl phosphates  Vinylogous amides  Tetrahydrofurans  Heteroaromatic compounds  Secondary alcohols  Lactams  Oxacyclic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Organic zwitterions  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents Purine 2'-deoxyribonucleoside triphosphate - Hypoxanthine - 6-oxopurine - Purine - Imidazopyrimidine - Pyrimidone - Aminopyrimidine - Alkyl phosphate - Pyrimidine - Phosphoric acid ester - Organic phosphoric acid derivative - N-substituted imidazole - Heteroaromatic compound - Vinylogous amide - Tetrahydrofuran - Imidazole - Azole - Secondary alcohol - Lactam - Oxacycle - Azacycle - Organic alkali metal salt - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organic zwitterion - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleoside triphosphates. These are purine nucleotides with triphosphate group linked to the ribose moiety lacking a hydroxyl group at position 2.
External Descriptors Not available

Names and Identifiers

Pubchem Sid 504773415
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504773415
IUPAC Name trisodium;[[[(2R,3S,5R)-5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl] hydrogen phosphate
INCHI InChI=1S/C10H16N5O13P3.3Na/c11-10-13-8-7(9(17)14-10)12-3-15(8)6-1-4(16)5(26-6)2-25-30(21,22)28-31(23,24)27-29(18,19)20;;;/h3-6,16H,1-2H2,(H,21,22)(H,23,24)(H2,18,19,20)(H3,11,13,14,17);;;/q;3*+1/p-3/t4-,5+,6+;;;/m0.../s1
InChIKey IWGGLKOTEOCWQP-BIHLCPNHSA-K
Smiles C1C(C(OC1N2C=NC3=C2N=C(NC3=O)N)COP(=O)([O-])OP(=O)([O-])OP(=O)(O)[O-])O.[Na+].[Na+].[Na+]
Isomeric SMILES C1[C@@H]([C@H](O[C@H]1N2C=NC3=C2N=C(NC3=O)N)COP(=O)([O-])OP(=O)([O-])OP(=O)(O)[O-])O.[Na+].[Na+].[Na+]
WGK Germany 3
Molecular Weight 573.13

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot Number Certificate Type Date Item
E2211191 Certificate of Analysis Feb 22, 2024 D112856
E2211197 Certificate of Analysis Feb 22, 2024 D112856
E2211205 Certificate of Analysis Feb 22, 2024 D112856
J1716081 Certificate of Analysis Apr 13, 2023 D112856

Chemical and Physical Properties

Molecular Weight 573.130 g/mol
XLogP3
Hydrogen Bond Donor Count 4
Hydrogen Bond Acceptor Count 15
Rotatable Bond Count 8
Exact Mass 572.942 Da
Monoisotopic Mass 572.942 Da
Topological Polar Surface Area 283.000 Ų
Heavy Atom Count 34
Formal Charge 0
Complexity 876.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 3
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 4

Solution Calculators

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