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Key Documents

96087

Sigma-Aldrich

N-Z-1,6-hexanediamine hydrochloride

≥97% (AT)

Synonym(s):

Benzyl N-(6-aminohexyl)carbamate hydrochloride, N-Z-1,6-diaminohexane hydrochloride

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About This Item

Linear Formula:
C6H5CH2OCONH(CH2)6NH2 · HCl
CAS Number:
Molecular Weight:
286.80
Beilstein/REAXYS Number:
4727129
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.22

assay

≥97% (AT)

form

crystals

reaction suitability

reagent type: cross-linking reagent

mp

175-180 °C

SMILES string

Cl[H].NCCCCCCNC(=O)OCc1ccccc1

InChI

1S/C14H22N2O2.ClH/c15-10-6-1-2-7-11-16-14(17)18-12-13-8-4-3-5-9-13;/h3-5,8-9H,1-2,6-7,10-12,15H2,(H,16,17);1H

InChI key

GMSZGOGHNFZOMF-UHFFFAOYSA-N

Other Notes

Introduction of a hexamethylenediamine linker[1]

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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M M Ponpipom et al.
Carbohydrate research, 113(1), 45-56 (1983-02-16)
Spacer arms 2.1-3.7 nm (21-37 A) long were prepared, and coupled with the methyl beta-glycoside of N-acetylmuramyl-L-alanyl-D-isoglutamine benzyl ester, to give blocked 6-acylates. Deprotection was effected with palladium chloride and triethyl-silane. Chemical conjugates of MDP-meningococcal group C polysaccharide were then

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