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242543

Sigma-Aldrich

Propylamine hydrochloride

≥99%

Sinonimo/i:

1-Aminopropane hydrochloride

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About This Item

Formula condensata:
CH3CH2CH2NH2·HCl
Numero CAS:
556-53-6
Peso molecolare:
95.57
Numero CE:
209-129-9
Numero MDL:
MFCD00012911
Codice UNSPSC:
12352100
ID PubChem:
24854566
NACRES:
NA.22

Livello qualitativo

200

Saggio

≥99%

Stato

solid

Punto di fusione

160-162 °C (lit.)

Solubilità

water: soluble 100 mg/mL, clear, colorless

Gruppo funzionale

amine

Stringa SMILE

Cl[H].CCCN

InChI

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

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Applicazioni

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

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302,H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
MKCM7029
MKCG8315
MKCC5779
MKCC0807
MKBZ0952V

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Sigma-Aldrich

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Trimethylamine hydrochloride

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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