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15406

Sigma-Aldrich

N-Boc-cadaverine

≥97.0% (NT)

Synonym(s):
N-Boc-1,5-diaminopentane, tert-Butyl N-(5-aminopentyl)carbamate
Linear Formula:
(CH)3COCONH(CH2)5NH2
CAS Number:
Molecular Weight:
202.29
Beilstein:
3603658
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥97.0% (NT)

reaction suitability

reagent type: cross-linking reagent
reagent type: spacer

refractive index

n20/D 1.460

density

0.972 g/mL at 20 °C (lit.)

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

Related Categories

Application

Some of the reported applications of N-Boc-cadaverine include:
  • 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).

Packaging

1, 5 mL in glass bottle

Other Notes

Building block for preparing polyamines and polyamides

Pictograms

Corrosion

Signal Word

Danger

Hazard 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

dust mask type N95 (US), Eyeshields, Gloves

Certificate of Analysis

Enter Lot Number to search for Certificate of Analysis (COA).

Certificate of Origin

Enter Lot Number to search for Certificate of Origin (COO).

More Documents

Quotes and Ordering

Articles

MRT - Mono-Boc-Protection of Diamines

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.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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