C55H77N7O14
1060.2 g/mol
Research ReagentDanger
(2S)-2-((2-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethylamino)-2-oxoethoxy)acetyl)amino)-N-(4-(hydroxymethyl)phenyl)-6-(((4-methoxyphenyl)-diphenylmethyl)amino)hexanamide
CAS1224601-12-0EC893-799-8
Category
Research Reagent
Compound Class
Amide
Primary Use
Research Compound
This compound is a PEGylated bifunctional linker reagent used in bioconjugation research. It features an azide group and a protected amino acid moiety, enabling site-specific modification of biomolecules.
Bioconjugation and labeling of biomoleculesPEGylation reagent for improving solubility and stability
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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Related Compounds
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Safety Reference
Danger
H225Highly flammable liquid and vapour
H304May be fatal if swallowed and enters airways
H315Causes skin irritation
H336May cause drowsiness or dizziness
H373May cause damage to organs through prolonged or repeated exposure
H412Harmful to aquatic life with long lasting effects
Customs Tariff Classification
The international HS code for (2S)-2-((2-(2-(2-(2-(2-(2-(2-(2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethoxy)ethylamino)-2-oxoethoxy)acetyl)amino)-N-(4-(hydroxymethyl)phenyl)-6-(((4-methoxyphenyl)-diphenylmethyl)amino)hexanamide (CAS 1224601-12-0) is 2929.90.
HS code (international, 6-digit)
2929.90
EU CN code (8-digit)
2929 90 90
Classification per the EU customs inventory ECICS (2026-07 snapshot, HS 2022). National tariff lines and product form can affect the final classification.
Identifiers
IUPAC Name
(2S)-2-[[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethylamino]-2-oxoethoxy]acetyl]amino]-N-[4-(hydroxymethyl)phenyl]-6-[[(4-methoxyphenyl)-diphenylmethyl]amino]hexanamide
InChIKey
PKUIBTBLKQVEJS-XHIZWQFQSA-N
SMILES
COC1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)NCCCC[C@@H](C(=O)NC4=CC=C(C=C4)CO)NC(=O)COCC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-]
Synonyms (5)
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