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437018

Sigma-Aldrich

N-Boc-1,6-hexanediamine hydrochloride

97%

Synonym(s):

N-Boc-1,6-diamino-hexane hydrochloride, tert-Butyl N-(6-aminohexyl)carbamate hydrochloride

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About This Item

Linear Formula:
(CH3)3COCONH(CH2)6NH2 · HCl
CAS Number:
65915-94-8
Molecular Weight:
252.78
Beilstein/REAXYS Number:
3631740
EC Number:
265-976-4
MDL number:
MFCD00039072
UNSPSC Code:
12352116
PubChem Substance ID:
24867340
NACRES:
NA.22

Quality Level

200

assay

97%

form

solid

reaction suitability

reagent type: cross-linking reagent

mp

162-164 °C (lit.)

functional group

Boc
amine

SMILES string

NCCCCCCNC(OC(C)(C)C)=O.[H]Cl

InChI

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

InChI key

JSBWQIZQJOQPFN-UHFFFAOYSA-N

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Related Categories

Application

N-Boc-1,6-hexanediamine hydrochloride is a general reagent to introduce a C6-spacer. It can be used in:
  • Synthesis of poly(L-glutamic acid) gadolinium chelates as biodegradable MRI contrast agents.
  • Synthesis of cholesteryl-functionalized hyaluronic acid-based anionic nanogel for protein delivery.
  • Preparation of amphiphilic prodrug, containing anticancer drug chlorambucil, which would self-assemble to form micelles in aqueous solution.

Reagent for the introduction of a C6-spacer.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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 and characterization of poly (L-glutamic acid) gadolinium chelate: a new biodegradable MRI contrast agent.
Wen X, et al.
Bioconjugate Chemistry, 15(6), 1408-1415 (2004)
Injectable hydrogel for sustained protein release by salt?induced association of hyaluronic acid nanogel.
Nakai T, et al.
Macromolecular Bioscience, 12(4), 475-483 (2012)
Rational Design of an Amphiphilic Chlorambucil Prodrug Realizing Self-Assembled Micelles for Efficient Anticancer Therapy.
Hu X, et al.
ACS biomaterials science & engineering, 4(3), 973-980 (2018)

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