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· · COA & SDS available for every product · Same-day shipping on in-stock items 5'-O-TBDMS-dA - ≥98% , CAS No.51549-30-5
Synonyms
AKOS030589348 | Adenosine, 2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]- | DTXSID10438072 | MS-25844 | (2R,3S,5R)-5-(6-Amino-9H-purin-9-yl)-2-(((tert-butyldimethylsilyl)oxy)methyl)tetrahydrofuran-3-ol | 5'-O-TBDMS-dA | HY-138599 | PD157771 | SCHEMBL17
Storage
Protected from light,Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Protected from light,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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview 5'-O-TBDMS-dA is a modified nucleoside and can be used to synthesize DNA or RNA.
Form:Solid
Specifications Synonyms
AKOS030589348 | Adenosine, 2'-deoxy-5'-O-[(1,1-dimethylethyl)dimethylsilyl]- | DTXSID10438072 | MS-25844 | (2R,3S,5R)-5-(6-Amino-9H-purin-9-yl)-2-(((tert-butyldimethylsilyl)oxy)methyl)tetrahydrofuran-3-ol | 5'-O-TBDMS-dA | HY-138599 | PD157771 | SCHEMBL17
Specifications & Purity
≥98%
Biochemical and Physiological Mechanisms
5'-O-TBDMS-dA is a modified nucleoside and can be used to synthesize DNA or RNA.
Storage
Protected from light,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 Smiles
CC(C)(C)[Si](C)(C)OCC1C(CC(O1)N2C=NC3=C(N=CN=C32)N)O
IUPAC Name
(2R,3S,5R)-5-(6-aminopurin-9-yl)-2-[[tert-butyl(dimethyl)silyl]oxymethyl]oxolan-3-ol
InChIKey
HGLRBQHXIBHZTD-QJPTWQEYSA-N
INCHI
1S/C16H27N5O3Si/c1-16(2,3)25(4,5)23-7-11-10(22)6-12(24-11)21-9-20-13-14(17)18-8-19-15(13)21/h8-12,22H,6-7H2,1-5H3,(H2,17,18,19)/t10-,11+,12+/m0/s1
Isomeric SMILES
CC(C)(C)[Si](C)(C)OC[C@@H]1[C@H](C[C@@H](O1)N2C=NC3=C(N=CN=C32)N)O
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Nucleosides, nucleotides, and analogues Class Purine nucleosides Subclass Purine 2'-deoxyribonucleosides Intermediate Tree Nodes Not available Direct Parent Purine 2'-deoxyribonucleosides Alternative Parents 6-aminopurines Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Trialkylheterosilanes Oxolanes Heteroaromatic compounds Silyl ethers Secondary alcohols Oxacyclic compounds Organic metalloid salts Azacyclic compounds Primary amines Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Purine 2'-deoxyribonucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - N-substituted imidazole - Imidolactam - Pyrimidine - Trialkylheterosilane - Heteroaromatic compound - Azole - Imidazole - Oxolane - Silyl ether - Secondary alcohol - Organoheterocyclic compound - Organic metalloid salt - Azacycle - Oxacycle - Organoheterosilane - Alcohol - Organic oxygen compound - Primary amine - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic metalloid moeity - Organic nitrogen compound - Amine - Organosilicon compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2. External Descriptors Not available Data sources 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.
3D Structure Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility DMSO : 100 mg/mL (273.60 mM; Need ultrasonic) Molecular Weight 365.500 g/mol XLogP3 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 5 Exact Mass 365.188 Da Monoisotopic Mass 365.188 Da Topological Polar Surface Area 108.000 Ų Heavy Atom Count 25 Formal Charge 0 Complexity 475.000 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 1
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