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Fmoc-N-amido-PEG9-acid

CAS No. CAS No.: 1191064-81-9
Cat No. Cat No.: BPG-2492
Purity Purity: ≥95%
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Fmoc-N-amido-PEG9-acid is a high-performance ADC linker featuring a PEG9 spacer that enhances solubility and flexibility. It facilitates efficient and stable drug-antibody conjugation, making it ideal for targeted cancer therapy development.

Category Fmoc-N-amido-PEGn-acid
Molecular Formula C36H53NO13
Molecular Weight 707.80
Appearance Pale Yellow or Colorless Oily Liquid
Shipping Room temperature
Storage Store at 2-8°C
Fmoc-N-amido-PEG9-acid

Structure of 1191064-81-9

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  • Specification
  • Key Product Attributes
  • Reaction & Conjugation Properties
Synonyms Fmoc-NH-PEG9-CH2CH2COOH; 1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13,16,19,22,25,28,31-decaoxa-4-azatetratriacontan-34-oic acid; Fmoc-NH-PEG9-acid; Fmoc-PEG9-propionic acid; 1-(Fmoc-amino)-3,6,9,12,15,18,21,24,27-nonaoxa-30-triacontanoic Acid; 5,8,11,14,17,20,23,26,29-Nonaoxa-2-azadotriacontanedioic acid 1-(9H-fluoren-9-ylmethyl) ester; 2,7,10,13,16,19,22,25,28,31-Decaoxa-4-azatetratriacontan-34-oic acid, 1-(9H-fluoren-9-yl)-3-oxo-
IUPACName 3-[2-[2-[2-[2-[2-[2-[2-[2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoic acid
CanonicalSMILES C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCC(=O)O
InChI InChI=1S/C36H53NO13/c38-35(39)9-11-41-13-15-43-17-19-45-21-23-47-25-27-49-28-26-48-24-22-46-20-18-44-16-14-42-12-10-37-36(40)50-29-34-32-7-3-1-5-30(32)31-6-2-4-8-33(31)34/h1-8,34H,9-29H2,(H,37,40)(H,38,39)
InChIKey NEESTRVILHNOJT-UHFFFAOYSA-N
BoilingPoint 803.9±65.0 °C at 760 mmHg
FlashPoint 440.0±34.3 °C
Purity ≥95%
Density 1.186±0.06 g/cm3 at 20°C, 760 Torr
Solubility Soluble in DCM, DMF, DMSO
RelatedCAS 850312-72-0 (polymer)
ShelfLife 0-4°C for short term (days to weeks), or -20°C for long term (months).
VaporPressure 0.0±3.0 mmHg at 25°C
LogP 0.51
PEGType Discrete PEG Linker
PEGArchitecture Linear
Functionality Monofunctional (Reactive)
ProtectingGroup Fmoc
ReactiveToward Primary Amines (after activation)
ReactionChemistry Carbodiimide-Mediated Amide Coupling (EDC/NHS)
BiomoleculeCompatibility Proteins / Antibodies; Peptides; Amine-Modified Oligonucleotides
ResearchUse Carboxyl-to-Amine Coupling after Activation; Amide Bond Formation

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