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Y0000063

Heptaminol hydrochloride

European Pharmacopoeia (EP) Reference Standard

Synonyme(s) :

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

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About This Item

Formule linéaire :
CH3CH(NH2)(CH2)3C(OH)(CH3)2 · HCl
Numéro CAS:
543-15-7
Poids moléculaire :
181.70
Numéro Beilstein :
3673011
Numéro MDL:
MFCD00013015
Code UNSPSC :
41116107
ID de substance PubChem :
329830831
Nomenclature NACRES :
NA.24

Qualité

pharmaceutical primary standard

Famille d'API

heptaminol

Fabricant/nom de marque

EDQM

Application(s)

pharmaceutical (small molecule)

Format

neat

Température de stockage

2-8°C

Chaîne 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

Clé InChI

JZNBMCOSOXIZJB-UHFFFAOYSA-N

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Catégories apparentées

Description générale

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.

Conditionnement

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

Autres remarques

Sales restrictions may apply.

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number

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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
Heptaminol interferes in the AxSYM FPIA amphetamine/methamphetamine II assay.
L Edno-Mcheik et al.
Clinical chemistry, 47(8), 1499-1500 (2001-07-27)
B Allard et al.
British journal of pharmacology, 104(3), 714-718 (1991-11-01)
1. Heptaminol stopped or delayed the progressive decline in tension which characterizes the phenomenon of fatigue in frog isolated twitch muscle fibre. 2. Heptaminol had no action on the sodium, potassium and calcium voltage-dependent ionic conductances. 3. The hypothesis of
Kanit Sumboonnanonda et al.
Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 87(2), 137-142 (2004-04-06)
The aim of this study was to assess the clinical efficacy, compliance and safety of Ginko biloba--Troxerutin-Heptaminol Hce in the treatment of patients with acute hemorrhoidal attacks in Thailand. In a prospective clinical study on hospital outpatients, the authors studied
Atul Pathak et al.
European journal of clinical pharmacology, 61(5-6), 471-474 (2005-07-02)
The aim of the present study was to investigate and characterise adverse drug reactions (ADRs) to drugs used in France for orthostatic hypotension (OH). In this prospective and systematic study, 121 consecutive out-patients suffering from primary (Parkinson's disease, pure autonomic
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