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M74253

N-Methyl-N-propargylbenzylamine

Name: <I>N</I>-Methyl-<I>N</I>-propargylbenzylamine
Brand: ALDRICH

97%

Synonym(s):

Pargyline

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About This Item

Linear Formula:

C₆H₅CH₂N(CH₃)CH₂C≡CH

CAS Number:

555-57-7

Molecular Weight:

159.23

NACRES:

NA.22

PubChem Substance ID:

24897164

UNSPSC Code:

12352100

EC Number:

209-101-6

MDL number:

MFCD00008576

Assay:

97%

Form:

liquid

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Properties

Quality Level

100

assay

97%

form

liquid

refractive index

n20/D 1.522 (lit.)

bp

86-88 °C/4 mmHg (lit.)

density

0.944 g/mL at 25 °C (lit.)

SMILES string

CN(CC#C)Cc1ccccc1

InChI

1S/C11H13N/c1-3-9-12(2)10-11-7-5-4-6-8-11/h1,4-8H,9-10H2,2H3

InChI key

DPWPWRLQFGFJFI-UHFFFAOYSA-N

Gene Information

human ... MAOA(4128), MAOB(4129)

Description

pictograms

GHS06

signalword

Danger

hcodes

H301 + H311 + H331,H315,H319,H335

pcodes

P261 - P280 - P301 + P310 - P302 + P352 + P312 - P304 + P340 + P311 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

183.2 °F - closed cup

flash_point_c

84 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Analysis of the levels of lysine-specific demethylase 1 (LSD1) mRNA in human ovarian tumors and the effects of chemical LSD1 inhibitors in ovarian cancer cell lines.

Sergiy Konovalov et al.

Journal of ovarian research, 6(1), 75-75 (2013-10-30)

Lysine-specific demethylase 1 (LSD1, also known as KDM1A and AOF2) is a chromatin-modifying activity that catalyzes the removal of methyl groups from lysine residues in histone and non-histone proteins, regulating gene transcription. LSD1 is overexpressed in several cancer types, and

Regiocontrolled construction of furo[3,2-c]pyran-4-one derivatives by palladium-catalyzed cyclization of propargylic carbonates with 4-hydroxy-2-pyrones.

Masahiro Yoshida et al.

The Journal of organic chemistry, 78(4), 1687-1692 (2013-02-01)

The reaction of propargylic carbonates with 4-hydroxy-2-pyrones in the presence of a palladium catalyst is described. By the choice of the reaction temperature, two types of the substituted furo[3,2-c]pyran-4-one derivatives were regioselectively synthesized, respectively.

Highly stereoselective synthesis of tertiary propargylic centers and their isomerization to enantiomerically enriched allenes.

José Luis García Ruano et al.

Chemistry (Weinheim an der Bergstrasse, Germany), 18(32), 9775-9779 (2012-08-01)

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Global Trade Item Number

SKU	GTIN
M74253-25G	04061837585234
M74253-5G	04061837585241