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Y0000063

Heptaminol hydrochloride

European Pharmacopoeia (EP) Reference Standard

Sinonimo/i:

6-Amino-2-methyl-2-heptanol hydrochloride, Heptaminol hydrochloride

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About This Item

Formula condensata:
CH3CH(NH2)(CH2)3C(OH)(CH3)2 · HCl
Numero CAS:
543-15-7
Peso molecolare:
181.70
Beilstein:
3673011
Numero MDL:
MFCD00013015
Codice UNSPSC:
41116107
ID PubChem:
329830831
NACRES:
NA.24

Grado

pharmaceutical primary standard

Famiglia di API

heptaminol

Produttore/marchio commerciale

EDQM

applicazioni

pharmaceutical (small molecule)

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

Cl.CC(N)CCCC(C)(C)O

InChI

1S/C8H19NO.ClH/c1-7(9)5-4-6-8(2,3)10;/h7,10H,4-6,9H2,1-3H3;1H
JZNBMCOSOXIZJB-UHFFFAOYSA-N

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Descrizione generale

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Applicazioni

Heptaminol hydrochloride EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Confezionamento

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Altre note

Sales restrictions may apply.

Prodotti correlati

N° Catalogo
Descrizione
Determinazione del prezzo

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

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F Seguin et al.
Magnetic resonance in medicine, 14(2), 396-400 (1990-05-01)
Moving average can be used to improve the signal-to-noise ratio of NMR kinetic studies. The method was tested on simulated spectra with time-dependent intensities or peak positions. It was then applied to a series of in vivo spectra, showing the
Emmanouil Lyris et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 827(2), 199-204 (2005-10-26)
A study of the metabolism of isometheptene, an antispasmodic drug, in man and comparison with heptaminol metabolism, is presented in this paper. Isometheptene and two metabolites were detected in human urine after oral administration of a tablet containing isometheptene mucate.
B Fontas et al.
Canadian journal of physiology and pharmacology, 68(7), 791-799 (1990-07-01)
Electrophysiological and transport effects induced by heptaminol hydrochloride were studied in frog epithelium. This tissue, which can easily be maintained in vitro, is a valuable model for studying sodium active transport with hormone-dependent characteristics that reproduce mammalian nephron behavior (notably
Heptaminol interferes in the AxSYM FPIA amphetamine/methamphetamine II assay.
L Edno-Mcheik et al.
Clinical chemistry, 47(8), 1499-1500 (2001-07-27)
A R Saha et al.
Research communications in chemical pathology and pharmacology, 67(3), 337-348 (1990-03-01)
Hepataminol AMP amidate (HAA), a nucleotide derivative possessing immunopotentiating activities, inhibited the mitogen-induced proliferation of murine splenocytes in vitro at the higher concentrations. Concanavalin A-induced mitogenic response was inhibited to 65 and 15% of the control value by HAA at
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