| Cas No.: | 1234369-95-9 |
| Chemical Name: | m-PEG8-aldehyde |
| Synonyms: | m-PEG8-aldehyde;m-PEG7-CH2CH2CHO;M-PEG8-CHO;m-dPEG(R)8-Propionaldehyde;alpha-Methoxy-omega-propanal octa(ethylene glycol);3-[2-[2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanal |
| SMILES: | O(C([H])([H])C([H])([H])OC([H])([H])C([H])([H])OC([H])([H])C([H])([H])OC([H])([H])C([H])([H])C([H])=O)C([H])([H])C([H])([H])OC([H])([H])C([H])([H])OC([H])([H])C([H])([H])OC([H])([H])C([H])([H])OC([H])([H])[H] |
| Formula: | C18O9H36 |
| M.Wt: | 396.4731 |
| Purity: | >98% |
| Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
| Description: | m-PEG7-CH2CH2CHO is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). |
| Target: | Non-cleavable |
| In Vitro: | ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker. |
| References: | [1]. Erwin R. Boghaert, et al. Anti-egfr antibody drug conjugates. WO2017214282A1. |

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