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Y0000063

Heptaminol hydrochloride

European Pharmacopoeia (EP) Reference Standard

Synonym(s):

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

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About This Item

Linear Formula:
CH3CH(NH2)(CH2)3C(OH)(CH3)2 · HCl
CAS Number:
543-15-7
Molecular Weight:
181.70
Beilstein/REAXYS Number:
3673011
MDL number:
MFCD00013015
UNSPSC Code:
41116107
PubChem Substance ID:
329830831
NACRES:
NA.24

grade

pharmaceutical primary standard

API family

heptaminol

manufacturer/tradename

EDQM

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

SMILES string

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

InChI key

JZNBMCOSOXIZJB-UHFFFAOYSA-N

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General description

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.

Application

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

Packaging

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

Other Notes

Sales restrictions may apply.

Related product

Product No.
Description
Pricing

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_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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