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dNTP (11) Nucleic acid related (20) PCR related (41)

Basic Description

Synonyms	Deoxythymidine 5'-triphosphate \| DTTP
Specifications & Purity	BioReagent, DNase, RNase free, PCR Reagent, endotoxin tested, UltraBio™, Suitable for molecular biology, sterile, for DNA and RNA applications, ≥99%, 100mM
Stability And Storage	Store at -20℃ long term (24 months). Upon delivery aliquot. Avoid freeze/thaw cycle.
Storage Temp	Store at -20°C,Avoid repeated freezing and thawing
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Grade	BioReagent, DNase, RNase free, endotoxin tested, for DNA and RNA applications, for molecular biology, PCR Reagent, sterile, UltraBio™
Product Description	Physical appearance:Liquid Storage buffer:Ultrapure water Description of products: dTTP (100mM, UltraPure) is a single-component of ultrapure dTTP, which is suitable for use in PCR, real-time PCR, RT-PCR, cDNA or DNA synthesis, primer extension reaction, DNA sequencing, DNA labeling, and other routine molecular biology reactions that require high-purity dNTP. The pH is titrated to 7.0-7.5 with NaOH solution. dNTP (Deoxy-ribonucleoside triphosphate) includes dATP (deoxyadenosine triphosphate), dCTP (deoxycytidine triphosphate), dGTP (deoxyguanosine triphosphate), dTTP (deoxythymidine triphosphate), and dUTP (deoxyuridine triphosphate). Among them, dATP, dCTP, dGTP and dTTP are indispensable in the PCR reaction as raw materials. DNA polymerase synthesizes a new DNA strand complementary to the DNA template strand by adding dNTPs that are complementary to the template in 5′ to 3′ direction, and thus the quality and concentration of dNTP are closely related to the amplification efficiency. Precautions: This product can be thawed at room temperature. Keep it on ice for use and store at -20℃ immediately after use. This product is for research use only, not for drug, clinical diagnosis, food, or other uses. For your safety and health, please wear a lab coat and disposable gloves during the operation.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
  - Class Pyrimidine nucleotides
    - Subclass Pyrimidine deoxyribonucleotides
      - Level5 Pyrimidine deoxyribonucleoside triphosphates
        Level6 Pyrimidine 2'-deoxyribonucleoside triphosphates

Kingdom	Organic compounds
Superclass	Nucleosides, nucleotides, and analogues
Class	Pyrimidine nucleotides
Subclass	Pyrimidine deoxyribonucleotides
Intermediate Tree Nodes	Pyrimidine deoxyribonucleoside triphosphates
Direct Parent	Pyrimidine 2'-deoxyribonucleoside triphosphates
Alternative Parents	Pyrimidones Alkyl phosphates Hydropyrimidines Vinylogous amides Heteroaromatic compounds Oxolanes Lactams Ureas Secondary alcohols Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic sodium salts Organic oxides Hydrocarbon derivatives Organic cations
Molecular Framework	Aromatic heteromonocyclic compounds
Substituents	Pyrimidine 2'-deoxyribonucleoside triphosphate - Pyrimidone - Hydropyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Oxolane - Heteroaromatic compound - Vinylogous amide - Lactam - Urea - Secondary alcohol - Organoheterocyclic compound - Azacycle - Organic alkali metal salt - Oxacycle - Organic nitrogen compound - Organic salt - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Alcohol - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic sodium salt - Organic cation - Aromatic heteromonocyclic compound
Description	This compound belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleoside triphosphates. These are pyrimidine nucleotides with a triphosphate group linked to the ribose moiety lacking a hydroxyl group at position 2.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

PH	7.0-7.5
IUPAC Name	trisodium;[[[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-oxidophosphoryl]oxy-oxidophosphoryl] hydrogen phosphate
INCHI	InChI=1S/C10H17N2O14P3.3Na/c1-5-3-12(10(15)11-9(5)14)8-2-6(13)7(24-8)4-23-28(19,20)26-29(21,22)25-27(16,17)18;;;/h3,6-8,13H,2,4H2,1H3,(H,19,20)(H,21,22)(H,11,14,15)(H2,16,17,18);;;/q;3*+1/p-3/t6-,7+,8+;;;/m0.../s1
InChIKey	KNVJTOALWGZWAI-SPSULGLQSA-K
Smiles	CC1=CN(C(=O)NC1=O)C2CC(C(O2)COP(=O)([O-])OP(=O)([O-])OP(=O)(O)[O-])O.[Na+].[Na+].[Na+]
Isomeric SMILES	CC1=CN(C(=O)NC1=O)[C@H]2C[C@@H]([C@H](O2)COP(=O)([O-])OP(=O)([O-])OP(=O)(O)[O-])O.[Na+].[Na+].[Na+]
Molecular Weight	548.11

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UltraPure dTTP (100mM) - BioReagent, DNase, RNase free, PCR Reagent, endotoxin tested, UltraBio™, Suitable for molecular biology, sterile, for DNA and RNA applications, ≥99%, 100mM, high purity , CAS No.18423-43-3