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Merck

Y0000063

Heptaminol hydrochloride

European Pharmacopoeia (EP) Reference Standard

Sinónimos:

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

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About This Item

Fórmula lineal:
CH3CH(NH2)(CH2)3C(OH)(CH3)2 · HCl
Número de CAS:
Peso molecular:
181.70
Beilstein:
3673011
Número MDL:
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
NACRES:
NA.24

grado

pharmaceutical primary standard

familia API

heptaminol

fabricante / nombre comercial

EDQM

aplicaciones

pharmaceutical (small molecule)

formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

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

Clave InChI

JZNBMCOSOXIZJB-UHFFFAOYSA-N

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Descripción general

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.

Aplicación

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

Envase

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

Otras notas

Sales restrictions may apply.

Producto relacionado

Referencia del producto
Descripción
Precios

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°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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