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Sigma-Aldrich

1-Adamantanmethylamin

98%

Synonym(e):

1-(Aminomethyl)-adamantan

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About This Item

Empirische Formel (Hill-System):
C11H19N
CAS-Nummer:
17768-41-1
Molekulargewicht:
165.28
MDL-Nummer:
MFCD00074750
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24850865

Qualitätsniveau

200

Assay

98%

Form

liquid

Brechungsindex

n20/D 1.5137 (lit.)

bp

83-85 °C/0.3 mmHg (lit.)

Dichte

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-

InChIKey

XSOHXMFFSKTSIT-BIBSGERRSA-N

Angaben zum Gen

human ... GRIN2A(2903)

Verwandte Kategorien

Allgemeine Beschreibung

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

Piktogramme

Corrosion
GHS05

Signalwort

Danger

H-Sätze

H314

Gefahreneinstufungen

Eye Dam. 1 - Skin Corr. 1B

Lagerklassenschlüssel

8A - Combustible, corrosive hazardous materials

WGK

WGK 3

Flammpunkt (°F)

197.6 °F - closed cup

Flammpunkt (°C)

92 °C - closed cup

Analysenzertifikate (COA)

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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
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.
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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