Atomfair 2′-Deoxyadenosine dA, 2′-dA C10H13N5O3 CAS 958-09-8

Description

2′-Deoxyadenosine (CAS: 958-09-8) is a nucleoside derivative and a fundamental building block of DNA, essential for molecular biology and biochemical research. With the molecular formula C₁₀H₁₃N₅O₃, it consists of adenine linked to a deoxyribose sugar via a β-N₉-glycosidic bond. This high-purity compound is widely utilized in nucleic acid synthesis, PCR applications, and enzymatic studies. Our product is rigorously tested for quality, ensuring optimal performance in sensitive assays. Available in anhydrous or monohydrate forms, it meets the stringent requirements of pharmaceutical, diagnostic, and academic research applications.

• CAS Number: 958-09-8
• Molecular Weight: 251.24 g/mol
• Purity: ≥99% (HPLC)
• Storage: Store at -20°C, protected from moisture

Properties

• CAS Number: 958-09-8
• Complexity: 307
• IUPAC Name: (2R,3S,5R)-5-(6-aminopurin-9-yl)-2-(hydroxymethyl)tetrahydrofuran-3-ol
• InChI: InChI=1S/C10H13N5O3/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(17)6(2-16)18-7/h3-7,16-17H,1-2H2,(H2,11,12,13)/t5-,6+,7+/m0/s1
• InChI Key: OLXZPDWKRNYJJZ-RRKCRQDMSA-N
• LogP: -0.55
• Exact Mass: 251.10183929
• Molecular Formula: C10H13N5O3
• Molecular Weight: 251.24
• SMILES: C1[C@@H]([C@H](O[C@H]1N2C=NC3=C(N=CN=C32)N)CO)O
• Topological: 119
• Monoisotopic Mass: 251.10183929
• Physical Description: White odorless crystals;
• Melting Point: 189 °C
• Synonyms: 2′-deoxyadenosine, deoxyadenosine, 958-09-8, Adenyldeoxyriboside, Adenine deoxyribose, ADENOSINE, 2′-DEOXY-, (2R,3S,5R)-5-(6-amino-9H-purin-9-yl)-2-(hydroxymethyl)tetrahydrofuran-3-ol, 2-Deoxyadenosine, Desoxyadenosine, Adenine deoxy nucleoside, CCRIS 1782, CHEBI:17256, AI3-52383, (2R,3S,5R)-5-(6-Aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-ol, 2-deoxy-adenosine, EINECS 213-488-7, NSC 83258, NSC 141848, NSC 143510, BRN 0091015, P582C98ULC, beta-D-erythro-Pentofuranoside, adenine-9 2-deoxy-, (2R,3S,5R)-5-(6-amino-9H-purin-9-yl)-2-(hydroxymethyl)oxolan-3-ol, 9H-Purin-6-amine, 9-(2-deoxy-beta-D-ribofuranosyl)-, 9-(2-Deoxy-beta-D-erythro-pentofuranosyl)adenine, 9H-Purin-6-amine, 9-(2-deoxy-beta-D-erythro-pentofuranosyl)-, beta-D-Ribofuranose, 1-(6-amino-9H-purin-9-yl)-1,2-dideoxy-, DTXSID10883624, 4-26-00-03589 (Beilstein Handbook Reference), 9-(2-deoxy-beta-D-ribofuranosyl)-9H-purin-6-amine, NSC-83258, NSC-141848, NSC-143510, 2′-DEOXYADENOSINE [USP IMPURITY], 9-(2-Deoxy-b-D-erythro-pentofuranosyl)adenine, adenine-9 2-deoxy-b-D-erythro-Pentofuranoside, Adenine-9 2-deoxy-beta-D-erythro-Pentofuranoside, 9-(2-deoxy-b-D-ribofuranosyl)-9H-Purin-6-amine, 9-(2-Deoxy-.beta.-D-erythro-pentofuranosyl)adenine, 9-(2-Deoxy-beta-delta-erythro-pentofuranosyl)adenine, adenine-9 2-deoxy-beta-delta-erythro-Pentofuranoside, 9-(2-deoxy-beta-delta-ribofuranosyl)-9H-Purin-6-amine, 1-(6-amino-9H-purin-9-yl)-1,2-dideoxy-b-D-Ribofuranose, 9-(2-deoxy-b-D-erythro-pentofuranosyl)-9H-Purin-6-amine, 1-(6-amino-9H-purin-9-yl)-1,2-dideoxy-beta-D-Ribofuranose, 9-(2-deoxy-beta-D-erythro-pentofuranosyl)-9H-Purin-6-amine, 1-(6-amino-9H-purin-9-yl)-1,2-dideoxy-beta-delta-Ribofuranose, 9-(2-deoxy-beta-delta-erythro-pentofuranosyl)-9H-Purin-6-amine, .beta.-D-Ribofuranose, 1-(6-amino-9H-purin-9-yl)-1,2-dideoxy-, 2′-DEOXYADENOSINE (USP IMPURITY), 5-(6-AMINO-PURIN-9-YL)-2-HYDROXYMETHYL-TETRAHYDRO-FURAN-3-OL, 9H-Purin-6-amine, 9-(2-deoxy-.beta.-D-erythro-pentofuranosyl)-, NSC83258, Adenosine, 2’deoxy, 2′-DEOXYADENOSINE [INCI], DTXCID701023135, 9HPurin6amine, 9(2deoxybetaDribofuranosyl), betaDerythroPentofuranoside, adenine9 2deoxy, 9HPurin6amine, 9(2deoxybetaDerythropentofuranosyl), betaDRibofuranose, 1(6amino9Hpurin9yl)1,2dideoxy, 213-488-7, 683-408-7, Adenine deoxyribonucleoside, Adenosine, 2′-deoxy,, MFCD00005754, Adenine deoxyriboside, 2′-dA, desoxyadenosin, 2′-Deoxyformycin A, 9-(2-Deoxy-|A-D-threo-pentofuranosyl)-9H-purin-6-amine, (2R,3S,5R)-5-(6-aminopurin-9-yl)-2-(hydroxymethyl)tetrahydrofuran-3-ol, (2r,3s,5r)-5-(6-Amino-9h-Purin-9-Yl)-Tetrahydro-2-(Hydroxymethyl)furan-3-Ol, 3D1, 2′-deoxy-d-adenosine, 9-(2-Deoxy-beta-D-ribofuranosyl)adenine, UNII-P582C98ULC, (3S,2R,5R)-5-(6-aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-ol, DNA nucleoside A, 2””-Deoxyadenosine, 2′-Deoxyadenosine Anhydrous, 2-Deoxyadenosine monohydrate, SCHEMBL19877, 2′-Deoxyadenosine (Standard), CHEMBL449329, GTPL5109, SCHEMBL3691593, ACon0_001347, BCP11997, HY-W040329R, BDBM50453912, MSK157318, SBB003141, AKOS015896793, 9-(2-Deoxy-b-D-ribofuranosyl)adenine, CS-W021069, HY-W040329, (R)-1-C-(7-Amino-1H-pyrazolo(4,3-d)pyrimidin-3-yl)-1,4-anhydro-2-deoxy-D-erythro-pentitol, 2′-Deoxyadenosine – isolated from DNA, 2′-Deoxyadenosine monohydrate, >=99%, NCGC00161970-01, 40627-14-3, AS-14314, FD158139, ST057079, 2 inverted exclamation marka-Deoxyadenosine, HY-154058, CS-0674964, D0046, NS00014680, Adenosine, 2′-deoxy- (6CI,7CI,8CI,9CI), C00559, EN300-108104, Q422457, 9-(2′-Deoxy-.beta.-D-erythro-pentofuranosyl)adenine, Z1416201984, D2DF2A54-B4A8-4727-A05C-3D1123687898, 2′-Deoxyadenosine monohydrate, powder, BioReagent, suitable for cell culture, 663188-78-1, D-erythro-Pentitol, 1-C-(7-amino-1H-pyrazolo(4,3-d)pyrimidin-3-yl)-1,4-anhydro-2-deoxy-, (R)-

2′-Deoxyadenosine is critical for DNA synthesis and repair studies, serving as a substrate for DNA polymerases. It is used in PCR amplification, sequencing, and oligonucleotide synthesis. Researchers also employ it to investigate nucleotide metabolism and enzyme kinetics. In pharmaceuticals, it aids in antiviral and anticancer drug development.

Safety and Hazards

GHS Hazard Statements

• H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]

Precautionary Statements

• P264, P270, P301+P316, P321, P330, P405, and P501

Hazard Classes and Categories

• Skin Irrit. 2 (75%)
• Eye Irrit. 2 (75%)
• STOT SE 3 (75%)

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