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Merck
CN

M74253

N-Methyl-N-propargylbenzylamine

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

Key Documents

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Product Name

N-Methyl-N-propargylbenzylamine, 97%

InChI key

DPWPWRLQFGFJFI-UHFFFAOYSA-N

InChI

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

SMILES string

CN(CC#C)Cc1ccccc1

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.)

Quality Level

100

Gene Information

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

Related Categories

pictograms

Skull and crossbones
GHS06

signalword

Danger

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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Certificates of Analysis (COA)

Lot/Batch Number
SDBB6706
STBB4251V
STBB4251
S43575
S31674

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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
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.
Francesca Reineri et al.
Journal of the American Chemical Society, 134(27), 11146-11152 (2012-06-06)
(15)N-Propargylcholine has been synthesized and hydrogenated with para-H(2). Through the application of a field cycling procedure, parahydrogen spin order is transferred to the (15)N resonance. Among the different isomers formed upon hydrogenation of (15)N-propargylcholine, only the nontransposed derivative contributes to
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)
Gangadhara R Sareddy et al.
Oncotarget, 4(1), 18-28 (2012-12-19)
Glioma development is a multistep process, involving alterations in genetic and epigenetic mechanisms. Understanding the mechanisms and enzymes that promote epigenetic changes in gliomas are urgently needed to identify novel therapeutic targets. We examined the role of histone demethylase KDM1
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