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242543

Sigma-Aldrich

Propylamin -hydrochlorid

≥99%

Synonym(e):

1-Amino-propan -hydrochlorid

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About This Item

Lineare Formel:
CH3CH2CH2NH2·HCl
CAS-Nummer:
556-53-6
Molekulargewicht:
95.57
EG-Nummer:
209-129-9
MDL-Nummer:
MFCD00012911
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24854566
NACRES:
NA.22

Assay

≥99%

Form

solid

mp (Schmelzpunkt)

160-162 °C (lit.)

Löslichkeit

water: soluble 100 mg/mL, clear, colorless

SMILES String

Cl[H].CCCN

InChI

1S/C3H9N.ClH/c1-2-3-4;/h2-4H2,1H3;1H

InChIKey

PYNUOAIJIQGACY-UHFFFAOYSA-N

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Anwendung

Propylamine hydrochloride was used to study the liquid chromatographic behavior of potassium-sparing and loop diuretics.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Ethylamin 97%

Sigma-Aldrich

301264

Ethylamin

Methylamin -hydrochlorid ≥98%

Sigma-Aldrich

M0505

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Triethylamin -hydrochlorid ≥99.0% (AT)

Sigma-Aldrich

90350

Triethylamin -hydrochlorid

Trimethylamin -hydrochlorid 98%

Sigma-Aldrich

T72761

Trimethylamin -hydrochlorid

F De Croo et al.
Journal of chromatography, 325(2), 395-411 (1985-06-07)
This paper deals with the specific identification of several thiazide, potassium-sparing and loop diuretics. The liquid chromatographic behaviour of these compounds is studied. Different organic modifiers (methanol, acetonitrile and tetrahydrofuran) are compared in terms of selectivity for the thiazide diuretics.
Rui Tao et al.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 39(8), 1996-2007 (2014-03-01)
Drug interaction between inhibitors of monoamine oxidase (MAOIs) and selective serotonin (5-hydroxytryptamine, 5-HT) reuptake (SSRIs) induces serotonin syndrome, which is usually mild but occasionally severe in intensity. However, little is known about neural mechanisms responsible for the syndrome induction and
M Figueiredo-González et al.
Food research international (Ottawa, Ont.), 106, 558-567 (2018-03-28)
In this work, phenol-rich extracts from 'Cornicabra' and 'Picual' virgin-olive oils (EVOOs) were examined, for the first time, to establish their capacity to inhibit key enzymes involved in Alzheimer's disease (AD) (acetylcholinesterase (AChE), butyrylcholinesterase (BuChE) and 5-lipoxygenase (LOX)), major depressive
Sarah W Black et al.
Biological psychiatry, 82(9), 623-633 (2016-12-07)
Narcolepsy, a disorder of rapid eye movement (REM) sleep, is characterized by excessive daytime sleepiness and cataplexy, a loss of muscle tone triggered by emotional stimulation. Current narcolepsy pharmacotherapeutics include controlled substances with abuse potential or drugs with undesirable side
Abu Bin Ihsan et al.
International journal of molecular sciences, 20(18) (2019-09-20)
A series of N-substituted poly(Gly-alter-Val) peptides were successfully synthesized for the systematic evaluation of the micellization behavior of alternating peptides. Three-component polymerization employing an aldehyde, a primary ammonium chloride, and potassium isocyanoacetate afforded four alternating peptides in excellent yields. We
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