Skip to Content
Merck
CN

79229

N-Boc-1,6-hexanediamine

≥98.0% (NT)

Synonym(s):

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

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C11H24N2O2
CAS Number:
51857-17-1
Molecular Weight:
216.32
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
57652779
MDL number:
MFCD00671489
Beilstein/REAXYS Number:
2219107
Assay:
≥98.0% (NT)
Form:
liquid

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

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)

SMILES string

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

InChI key

RVZPDKXEHIRFPM-UHFFFAOYSA-N

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

Quality Level

200

Related Categories

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
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

257.0 °F - closed cup

flash_point_c

125 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCK7692
BCCC4552
BCBR1438V
BCBL6617V
BCBF8199V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis, penetrability and intracellular targeting of fluorescein-tagged peptoids and peptide?peptoid hybrids
Unciti-Broceta A, et al.
Bioorganic & Medicinal Chemistry, 17(3), 959-966 (2009)
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)
Preparation of mixed self-assembled monolayers (SAMs) that resist adsorption of proteins using the reaction of amines with a SAM that presents interchain carboxylic anhydride groups.
Chapman R G, et al.
Langmuir, 16(17), 6927-6936 (2000)
Yan Wang et al.
Journal of controlled release : official journal of the Controlled Release Society, 328, 970-984 (2020-09-15)
To avoid poly(ethylene glycol)-related issues of nanomedicines such as accelerated blood clearance, fully N-2-hydroxypropyl methacrylamide (HPMAm)-based polymeric micelles decorated with biotin for drug delivery were designed. To this end, a biotin-functionalized chain transfer agent (CTA), 4-cyano-4-[(dodecylsulfanylthiocarbonyl)-sulfanyl]pentanoic acid (biotin-CDTPA), was synthesized
Construction of a well-defined multifunctional dendrimer for theranostics.
Ornelas C, et al.
Organic Letters, 13(5), 976-979 (2011)
View All Related Papers

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

Contact Technical Service