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Merck

94200

Sigma-Aldrich

Undecylamine

≥98.0% (GC)

Sinónimos:

1-Amino-undecane

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About This Item

Fórmula lineal:
CH3(CH2)10NH2
Número de CAS:
Peso molecular:
171.32
Beilstein/REAXYS Number:
1736378
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

≥98.0% (GC)

form

liquid

refractive index

n20/D 1.439 (lit.)
n20/D 1.439

bp

106-107 °C/8 mmHg (lit.)
240 °C (lit.)

mp

15-17 °C (lit.)

density

0.796 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

CCCCCCCCCCCN

InChI

1S/C11H25N/c1-2-3-4-5-6-7-8-9-10-11-12/h2-12H2,1H3

InChI key

QFKMMXYLAPZKIB-UHFFFAOYSA-N

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signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

197.6 °F - closed cup

flash_point_c

92 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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X-type ligands, for example, the pair of oleylamine (OAm) and oleic acid (OA), have been widely used to prepare CsPbX3 nanocrystals (NCs). However, the proton exchange between coordinated OAm and OA may induce the detachment of ligands, resulting in poor
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The present work explores the possibility of chemically modifying carboxymethyl cellulose (CMC), a widely diffused commercial cellulose ether, by grafting of hydrophobic moieties. Amidation of CMC, at high temperature and in heterogeneous conditions, was selected as synthetic tool for grafting
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Using a combined synthesis approach comprising reversible addition-fragmentation transfer polymerization and ring opening reaction, a series of poly glycidyl methacrylate (polyGMA) polymers were designed and synthesized for gene delivery. These polymers characterized by low cationic charge respective to established gene

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