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180378

Sigma-Aldrich

1-Adamantanemethylamine

98%

Synonym(s):

1-(Aminomethyl)adamantane

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About This Item

Empirical Formula (Hill Notation):
C11H19N
CAS Number:
17768-41-1
Molecular Weight:
165.28
MDL number:
MFCD00074750
UNSPSC Code:
12352100
PubChem Substance ID:
24850865
NACRES:
NA.22

Quality Level

200

Assay

98%

form

liquid

refractive index

n20/D 1.5137 (lit.)

bp

83-85 °C/0.3 mmHg (lit.)

density

0.933 g/mL at 25 °C (lit.)

SMILES string

NCC12C[C@H]3C[C@H](C[C@H](C3)C1)C2

InChI

1S/C11H19N/c12-7-11-4-8-1-9(5-11)3-10(2-8)6-11/h8-10H,1-7,12H2/t8-,9+,10-,11-

InChI key

XSOHXMFFSKTSIT-BIBSGERRSA-N

Gene Information

human ... GRIN2A(2903)

Related Categories

General description

1-Adamantanemethylamine is a large amine present on the wall of 6,7-diaminoquinoxaline. The thermodynamic complex formation constant of 1-adamantanemethylamine was studied.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Regulatory Information

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Certificates of Analysis (COA)

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Seunghyun Lee et al.
Colloids and surfaces. B, Biointerfaces, 147, 281-290 (2016-08-16)
Albumin has been viewed as one of the most attractive biomacromolecules for making nanoparticulate systems due to its biocompatibility and chemical functionality. Thus far, albumin nanoparticles (NPs) are prepared by several limited methods, such as, desolvation, emulsification or high-pressure homogenization.
Shengxiong Xiao et al.
Chemical communications (Cambridge, England), 46(14), 2459-2461 (2010-04-10)
The condensation of a Kemp's triacid derivative with a diamino resorcinarene yielded a cavitand with the deepest cavity prepared to date featuring an inwardly-directed carboxylic acid. The extended 6,7-diaminoquinoxaline wall bearing the acid allowed accommodation of large amines, such as
Joachim F R Van Guyse et al.
Polymers, 13(3) (2021-02-04)
Smart or adaptive materials often utilize stimuli-responsive polymers, which undergo a phase transition in response to a given stimulus. So far, various stimuli have been used to enable the modulation of drug release profiles, cell-interactive behavior, and optical and mechanical
Haibao Jin et al.
Biopolymers, 110(4), e23258-e23258 (2019-01-25)
Due to the branched structure feature and unique properties, a variety of star-shaped polymers have been designed and synthesized. Despite those advances, solid-phase synthesis of star-shaped sequence-defined synthetic polymers that exhibit hierarchical self-assembly remains a significant challenge. Hence, we present

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