15406
N-Boc-cadaverine
≥97.0% (NT)
Synonym(s):
N-Boc-1,5-diaminopentane, tert-Butyl N-(5-aminopentyl)carbamate
About This Item
Recommended Products
Quality Level
Assay
≥97.0% (NT)
reaction suitability
reagent type: cross-linking reagent
refractive index
n20/D 1.460
density
0.972 g/mL at 20 °C (lit.)
functional group
Boc
amine
SMILES string
NCCCCCNC(OC(C)(C)C)=O
InChI
1S/C10H22N2O2/c1-10(2,3)14-9(13)12-8-6-4-5-7-11/h4-8,11H2,1-3H3,(H,12,13)
InChI key
DPLOGSUBQDREOU-UHFFFAOYSA-N
Application
- Synthesis of of a supermacrocycle that self-assemble to form organic nanotubes.
- Preparation of water-soluble unsymmetrical sulforhodamine fluorophores from monobrominated sulfoxanthene dye.
- Synthesis of functionalized porphyrins as biocompatible carrier system for photodynamic therapy (PDT).
Other Notes
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
228.2 °F - closed cup
Flash Point(C)
109.0 °C - closed cup
Personal Protective Equipment
Certificates of Analysis (COA)
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Articles
Mono-Boc-protected diamines are versatile building blocks for chemical synthesis. Their production is a lot more challenging than the simple reaction scheme might imply, because the Boc-anhydride reagent cannot differentiate between the two identical amino moieties in the substrate.
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