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79229

Sigma-Aldrich

N-Boc-1,6-hexanediamine

≥98.0% (NT)

Synonym(s):

N-Boc-1,6-diaminohexane, tert-Butyl-N-(6-aminohexyl)carbamate

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About This Item

Empirical Formula (Hill Notation):
C11H24N2O2
CAS Number:
Molecular Weight:
216.32
Beilstein:
2219107
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22

Assay

≥98.0% (NT)

form

liquid

reaction suitability

reagent type: cross-linking reagent

refractive index

n20/D 1.462

density

0.965 g/mL at 20 °C (lit.)

functional group

Boc
amine

SMILES string

NCCCCCCNC(OC(C)(C)C)=O

InChI

1S/C11H24N2O2/c1-11(2,3)15-10(14)13-9-7-5-4-6-8-12/h4-9,12H2,1-3H3,(H,13,14)

InChI key

RVZPDKXEHIRFPM-UHFFFAOYSA-N

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Application

N-Boc-1,6-hexanediamine can be used as a linear hexyl spacer (C6-spacer) to synthesize:
  • Biodegradable poly(disulfide amine)s for gene delivery.
  • A multifunctional dendrimer for theranostics.
  • Polyamide platinum anti-cancer complexes designed to target cancer specific DNA sequences.
  • Self-assembled monolayers (SAMs) that resist adsorption of proteins.
  • [N-(6-(4-Hydroxy-6-isopropylamino-1,3,5-triazin-2-ylamino)hexyl)-5-hydroxy-1,4-naphthoquinone-3-propionamide] (JUG-HATZ), which can be used in designing electrochemical immunosensors.
Reagent for the introduction of a C6-spacer.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

257.0 °F - closed cup

Flash Point(C)

125 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis, penetrability and intracellular targeting of fluorescein-tagged peptoids and peptide?peptoid hybrids
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Design and synthesis of substrates for newborn screening of Maroteaux?Lamy and Morquio A syndromes.
Duffey TA, et al.
Bioorganic & Medicinal Chemistry, 20(20), 5994-5996 (2010)
Polyamide platinum anticancer complexes designed to target specific DNA sequences.
Jaramillo, et al.
Inorganic Chemistry, 45(15), 6004-6013 (2006)
Haonan Xing et al.
Colloids and surfaces. B, Biointerfaces, 182, 110355-110355 (2019-07-16)
Inspired by the excellent membrane affinity of antimicrobial polymers, we synthesized a novel biodegradable poly(amino amine) polymer with pendent side chains that mimic the widely used biocide polyhexamethylene biguanide (PHMB) for gene delivery. Michael addition polymerization was utilized to form
A label-free electrochemical immunosensor for direct, signal-on and sensitive pesticide detection.
Tran HV, et al.
Biosensors And Bioelectronics, 31(1), 62-68 (2012)

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