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BX LAB PRODUCT CATEGORY

Ara Nucleosides

Quick view. Arabinonucleosides and protected intermediates for antiviral, oncology and modified-oligonucleotide chemistry. This category currently includes 28 products. Ara Nucleosides products serve as starting materials, protected intermediates and analytical comparators in nucleoside, nucleotide and oligonucleotide chemistry.

Products28
Use scopeResearch use only
Pack sizeCustomized to requirements
SupportSelection and custom synthesis review

Category guide

Typical use

Ara Nucleosides products serve as starting materials, protected intermediates and analytical comparators in nucleoside, nucleotide and oligonucleotide chemistry.

How to select

Confirm anomeric and sugar stereochemistry, base identity, substitution position, protecting-group pattern and required downstream transformation.

How to qualify

Use orthogonal identity data such as NMR and MS together with chromatographic purity, water or residual-solvent review and route-specific impurity controls.

Product-family considerations

Common advantages
  • Nucleoside catalogs provide flexible entry points for protecting-group, phosphorylation and glycosylation-route development.
  • Availability of related analogs helps researchers compare base, sugar and substitution effects systematically.
Common limitations
  • Downstream use often requires additional protection, activation or purification before incorporation into oligonucleotide workflows.
  • Isomeric purity, water content and residual solvents should be matched to the planned chemistry.

Category literature

These publications provide background for the Ara Nucleosides product family. Individual product pages only show additional product- or feature-relevant references.

Selection checklist

Exact identityMatch the canonical name with a CAS number, structure, SMILES or drawing; confirm stereochemistry, protecting groups and salt form where applicable.
SpecificationDefine target purity, analytical method, water or residual-solvent concerns and any application-specific acceptance limits.
Workflow fitShare the reaction, enzyme, sequence, solvent system, support or analytical method used to evaluate compatibility.
Supply needProvide initial quantity, expected future scale, packaging preference, timeline and documentation requirements.

28 products

Chemical structure of N4-MethylarabinocytidineN4-Methylarabinocytidine

≥98% · CAS: 13491-42-4

BX-ARN-0004
Chemical structure of 2'-Amino-2'-deoxy-beta-D-arabino-5-methyluridine2'-Amino-2'-deoxy-beta-D-arabino-5-methyluridine

≥98% · CAS: 135304-48-2

BX-ARN-0023
Chemical structure of 4-Chloro-7-(3',5'-di-O-benzoyl-2'-deoxy-2'-fluoro-beta-D-arabinofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine4-Chloro-7-(3',5'-di-O-benzoyl-2'-deoxy-2'-fluoro-beta-D-arabinofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine

≥98% · CAS: 169516-55-6

BX-ARN-0024
Chemical structure of 4-Chloro-7-(2'-deoxy-2'-fluoro-beta-D-arabinofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine4-Chloro-7-(2'-deoxy-2'-fluoro-beta-D-arabinofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine

≥98% · CAS: 169516-60-3

BX-ARN-0025
Chemical structure of 4-Amino-7-(2'-deoxy-2'-fluoro-beta-D-arabinofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine4-Amino-7-(2'-deoxy-2'-fluoro-beta-D-arabinofuranosyl)-7H-pyrrolo[2,3-d]pyrimidine

≥98% · CAS: 169516-61-4

BX-ARN-0026
Chemical structure of N4-AcetylarabinocytidineN4-Acetylarabinocytidine

≥98% · CAS: 13491-47-9

BX-ARN-0005
Chemical structure of 5,6-Dihydro-ara-uridine5,6-Dihydro-ara-uridine

≥98% · CAS: 30100-83-5

BX-ARN-0015
Chemical structure of 5-Bromoarabinouridine5-Bromoarabinouridine

≥98% · CAS: 3370-69-2

BX-ARN-0031
Chemical structure of N4,N4-DimethylarabinocytidineN4,N4-Dimethylarabinocytidine

≥98% · CAS: 82855-64-9

BX-ARN-0019
Chemical structure of 3,5-Dimethyl-beta-D-arabinouridine3,5-Dimethyl-beta-D-arabinouridine

99.98% · CAS: 887113-66-8

BX-ARN-0021
Structure of vidarabine (adenine arabinoside)Vidarabine

≥98% · CAS: 5536-17-4

BX-NDO-0016
Structure of 9-beta-D-arabinofuranosylguanine9-beta-D-Arabinofuranosylguanine

≥98% · CAS: 38819-10-2

BX-NDO-0017
Chemical structure of arauridineArauridine

≥98% · CAS: 3083-77-0

BX-NDO-0022
Structure of BX-ARN-0028Fludarabine

≥98% · CAS: 21679-14-1

BX-ARN-0028
Chemical structure of 5-Iodoarabinouridine5-Iodoarabinouridine

≥98% · CAS: 3052-06-0

BX-ARN-0030
Chemical structure of 2'-Amino-2'-deoxy-beta-D-arabinouridine2'-Amino-2'-deoxy-beta-D-arabinouridine

≥98% · CAS: 68115-81-1

BX-ARN-0032
Chemical structure of 5-Hydroxy-beta-D-arabinouridine5-Hydroxy-beta-D-arabinouridine

≥98% · CAS: 69321-95-5

BX-ARN-0017
Chemical structure of 8-Chloro-arabinoadenosine8-Chloro-arabinoadenosine

≥98% · CAS: 769872-68-6

BX-ARN-0033
Chemical structure of N6-Benzoyl-arabinoadenosineN6-Benzoyl-arabinoadenosine

≥98% · CAS: 79896-97-2

BX-ARN-0018
Chemical structure of 5'-O-DMT-2',N4-diacetyl-beta-D-arabinofuranosyl-cytosine5'-O-DMT-2',N4-diacetyl-beta-D-arabinofuranosyl-cytosine

≥98% · CAS: 120401-14-1

BX-ARN-0003
Chemical structure of 5'-O-DMT-2'-O-acetyl-beta-D-arabinofuranosyl-uracil5'-O-DMT-2'-O-acetyl-beta-D-arabinofuranosyl-uracil

≥98% · CAS: 173099-62-2

BX-ARN-0006
Chemical structure of 3-methyl-1-beta-D-arabinofuranosyluracil3-Methyl-1-beta-D-arabinofuranosyluracil

≥98% · CAS: 17676-62-9

BX-ARN-0007
Chemical structure of N2-isobutyryl-beta-D-arabinofuranosylguanosineN2-Isobutyryl-beta-D-arabinofuranosylguanosine

≥98% · CAS: 199601-35-9

BX-ARN-0008
Structure of BX-ARN-00101,N6-Etheno-ara-adenosine

≥98% · CAS: 2095417-09-5

BX-ARN-0010
Structure of 2'-Amino-2'-deoxy-5-fluoro-arabinouridine BX-ARN-00292'-Amino-2'-deoxy-5-fluoro-arabinouridine

≥98% · CAS: 2305415-81-8

BX-ARN-0029
Structure of 2',3',5'-Tri-O-benzyl-4'-thio-arabinouridine BX-ARN-00112',3',5'-Tri-O-benzyl-4'-thio-arabinouridine

≥98% · CAS: 267665-69-0

BX-ARN-0011
Chemical structure of 5'-O-DMT-2'-acetyl-N6-benzoyl-β-D-arabinofuranosyl-adenine5'-O-DMT-2'-acetyl-N6-benzoyl-β-D-arabinofuranosyl-adenine

≥98% · CAS: 2756253-84-4

BX-ARN-0012
Chemical structure of 5-Hydroxymethyl-arabino-uridine5-Hydroxymethyl-arabino-uridine

≥98% · CAS: 28608-82-4

BX-ARN-0013

Frequently asked questions

What are typical uses for Ara Nucleosides?

Ara Nucleosides products serve as starting materials, protected intermediates and analytical comparators in nucleoside, nucleotide and oligonucleotide chemistry.

What should be confirmed before ordering Ara Nucleosides?

Confirm anomeric and sugar stereochemistry, base identity, substitution position, protecting-group pattern and required downstream transformation.

Are custom quantities or related analogs available?

BX Lab reviews custom package sizes, catalog-adjacent analogs and research-use custom synthesis requests against the target structure, purity, scale and timeline.

Need help selecting a product?

Tell our scientists about your target chemistry, workflow, required purity and scale. We can help identify a catalog product, related analog or custom route.

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