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270083

Sigma-Aldrich

9-(Methylaminomethyl)anthracene

99%

Synonym(s):

(Anthracen-9-ylmethyl)-N-methylamine, 1-Anthracen-9-yl-N-methylmethanamine, 9-(N-Methylaminomethyl)anthracene, N-Methyl-9-anthracenemethanamine

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About This Item

Empirical Formula (Hill Notation):
C16H15N
CAS Number:
73356-19-1
Molecular Weight:
221.30
MDL number:
MFCD00009933
UNSPSC Code:
12352100
PubChem Substance ID:
24856352
NACRES:
NA.22

Assay

99%

form

solid

mp

57-59 °C (lit.)

storage temp.

2-8°C

SMILES string

CNCc1c2ccccc2cc3ccccc13

InChI

1S/C16H15N/c1-17-11-16-14-8-4-2-6-12(14)10-13-7-3-5-9-15(13)16/h2-10,17H,11H2,1H3

InChI key

WRVHTDZJMNUGQN-UHFFFAOYSA-N

Related Categories

General description

9-(Methylaminomethyl)anthracene is an isocyanate derivatizing reagent.

Application

9-(Methylaminomethyl)anthracene (MAMA) was used as a model drug in the study of the effect of enzymatic degradation on the release behaviors of MAMA by UV-Vis spectroscopy. It was also used as a reagent in a sensitive method for determination of isocyanates in air by HPLC via UV or fluorescence detection.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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X Y Xiong et al.
Journal of controlled release : official journal of the Controlled Release Society, 108(2-3), 263-270 (2005-10-04)
Poly(lactic acid) (PLA) was successfully grafted to both ends of Pluronic F127 block copolymer (PEO-PPO-PEO) to obtain amphiphilic PLA-F127-PLA block copolymers. The effect of enzymatic degradation on the release behaviors of hydrophobic model drug 9-(methylaminomethyl)anthracene (MAMA) from PLA-F127-PLA nano-particles with
Journal of Liquid Chromatography, 3, 971-971 (1980)
R P Streicher et al.
American Industrial Hygiene Association journal, 57(10), 905-913 (1996-10-01)
Analytical reference standards generally are not available for non-monomeric isocyanate species, making accurate identification and quantitation by high-performance liquid chromatography (HPLC) difficult. A successful derivatizing reagent must react rapidly with all isocyanate groups, the derivatized isocyanate must be detectable selectively

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