Direkt zum Inhalt
Merck
Alle Fotos(1)

Key Documents

View All Documentation

M74253

Sigma-Aldrich

N-Methyl-N-Propargylbenzylamin

97%

Synonym(e):

Pargylin

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(1)

About This Item

Lineare Formel:
C6H5CH2N(CH3)CH2C≡CH
CAS-Nummer:
555-57-7
Molekulargewicht:
159.23
EG-Nummer:
209-101-6
MDL-Nummer:
MFCD00008576
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24897164
NACRES:
NA.22

Assay

97%

Form

liquid

Brechungsindex

n20/D 1.522 (lit.)

bp

86-88 °C/4 mmHg (lit.)

Dichte

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

InChIKey

DPWPWRLQFGFJFI-UHFFFAOYSA-N

Angaben zum Gen

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

Piktogramme

Skull and crossbones
GHS06

Signalwort

Danger

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

183.2 °F - closed cup

Flammpunkt (°C)

84 °C - closed cup

Persönliche Schutzausrüstung

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
STBB4251V
STBB4251
S43575
S31674
13320JF

Die passende Version wird nicht angezeigt?

Wenn Sie eine bestimmte Version benötigen, können Sie anhand der Lot- oder Chargennummer nach einem spezifischen Zertifikat suchen.

Suche nach COA

Besitzen Sie dieses Produkt bereits?

In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

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)
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.
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
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
Alle zugehörigen Dokumente anzeigen

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

Setzen Sie sich mit dem technischen Dienst in Verbindung.