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Merck
CN

94200

Undecylamine

≥98.0% (GC)

Synonym(s):

1-Amino-undecane

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About This Item

Linear Formula:
CH3(CH2)10NH2
CAS Number:
7307-55-3
Molecular Weight:
171.32
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24889778
EC Number:
230-761-6
Beilstein/REAXYS Number:
1736378
MDL number:
MFCD00008152
Assay:
≥98.0% (GC)
Form:
liquid

Key Documents

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InChI key

QFKMMXYLAPZKIB-UHFFFAOYSA-N

InChI

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

SMILES string

CCCCCCCCCCCN

assay

≥98.0% (GC)

form

liquid

refractive index

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

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

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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Certificates of Analysis (COA)

Lot/Batch Number
1258868V
1258868
044862/1
043615/1
042756/1

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The degree of counterion binding (β) to micelles of aqueous n-alkylammonium chlorides (C
Qixuan Zhong et al.
Nano letters, 19(6), 4151-4157 (2019-05-24)
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
Jonathan O'Keeffe Ahern et al.
Biomacromolecules, 19(5), 1410-1415 (2017-11-11)
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
Asja Pettignano et al.
Polymers, 11(7) (2019-07-26)
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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