Succinates
N6-Bz-DMTr-2'-OMe-A-3'-succinate, TEA salt
Quick view. A protected N6-benzoyl 2'-O-methyladenosine 3'-succinate triethylamine salt for research-use oligonucleotide-synthesis workflows. CAS 2940857-85-0. Catalog target purity: ≥98%. Availability: Inquiry only — contact BX Lab to confirm current availability.
Identifier context
These notes preserve the current catalog identifiers while making their review boundary explicit.
The listed InChIKey and structure image represent the reviewed parent/free-acid moiety. The triethylammonium counterion is not depicted; confirm the exact supplied salt form with BX Lab.
Product profile
N6-Bz-DMTr-2'-OMe-A-3'-succinate, TEA salt is classified as succinates.
N6-Bz-DMTr-2'-OMe-A-3'-succinate, TEA salt — Protected 2'-O-methyl adenosine succinate intermediate for research-use oligonucleotide-synthesis workflows.
For N6-Bz-DMTr-2'-OMe-A-3'-succinate, TEA salt, excessive or poorly positioned substitution can reduce desired enzyme interactions or activity in some assay formats.
Names and search terms
Confirmed or normalized name variants
- 2'-OMe-A(Bz) 3'-succinate, Triethylammonium salt
- DMT-2'-O-Me-A(Bz)-3'-succinate, TEA salt
- N6-benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-methyladenosine-3'-O-succinate, triethylamine salt
- BRP-01226
Useful catalog search terms
- N6-Bz-DMTr-2'-OMe-A-3'-succinate TEA salt
- 2940857-85-0
- PubChem CID 168446487
- DMT-2'-O-Me-A(Bz)-3'-succinate
Physicochemical data
| CAS context | Parent/free-acid identity |
|---|---|
| Parent molecular formula | C43H41N5O10 |
| Parent molecular weight | 787.80 |
| TEA salt molecular formula | C49H56N6O10 |
| TEA salt molecular weight | 889.02 |
| PubChem CID | 168446487 |
| InChIKey | JGEUBEGMIVEEBB-FXTDJBBPSA-N |
| Nucleoside | N6-benzoyl 2'-O-methyladenosine |
| 3'-O group | Succinate |
| 5'-O group | DMTr |
| Salt form | Triethylamine salt |
| InChI | InChI=1S/C43H41N5O10/c1-53-31-18-14-29(15-19-31)43(28-12-8-5-9-13-28,30-16-20-32(54-2)21-17-30)56-24-33-37(58-35(51)23-22-34(49)50)38(55-3)42(57-33)48-26-46-36-39(44-25-45-40(36)48)47-41(52)27-10-6-4-7-11-27/h4-21,25-26,33,37-38,42H,22-24H2,1-3H3,(H,49,50)(H,44,45,47,52)/t33-,37-,38-,42-/m1/s1 |
| SMILES | CO[C@@H]1[C@@H]([C@H](O[C@H]1N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4)COC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC)OC(=O)CCC(=O)O |
| Canonical SMILES | CO[C@@H]1[C@@H]([C@H](O[C@H]1N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4)COC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC)OC(=O)CCC(=O)O |
| Structure representation | Parent/free-acid protected nucleoside-succinate moiety; triethylammonium counterion is not depicted |
| InChIKey review status | The listed InChIKey and structure image represent the reviewed parent/free-acid moiety. The triethylammonium counterion is not depicted; confirm the exact supplied salt form with BX Lab. |
Release documentation
The current specification defines the analytical method and acceptance criteria; the released lot result is reported on the CoA.
Additional HPLC, MS or NMR documentation can be agreed during technical review where available.
Product-specific evaluation notes
Potential advantages
- 2′-O-methyl groups are widely used to increase nuclease resistance and modulate hybridization behavior.
Method limitations
- Excessive or poorly positioned substitution can reduce desired enzyme interactions or activity in some assay formats.
These points describe N6-Bz-DMTr-2'-OMe-A-3'-succinate, TEA salt or its named chemical feature. Broader product-family guidance is maintained on the category page.
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Frequently asked questions
Can the package size for N6-Bz-DMTr-2'-OMe-A-3'-succinate, TEA salt be customized?
Yes. Share the initial quantity, expected future scale, delivery timeline and packaging preference for review.
What information should be included in a quote request?
Quote catalog number BX-SUCC-0009 and CAS 2940857-85-0, the intended research workflow, required quantity and any additional HPLC, MS or NMR documentation needed.
Product-family literature
These publications provide peer-reviewed context for the Succinates product family and its named chemistry. They are background reading only, not evidence for the exact product, supplied form, lot specification, availability or performance.
Technology platforms
Catalog-derived platform membership for navigating related chemistry and verifiable product sets.