Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

113727

Sigma-Aldrich

Norphenylephrine hydrochloride

98%

Synonym(s):

α-Aminomethyl-3-hydroxybenzyl alcohol hydrochloride, 3,α-Dihydroxyphenethylamine hydrochloride, Norfenefrine hydrochloride

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
HOC6H4CH(CH2NH2)OH · HCl
CAS Number:
4779-94-6
Molecular Weight:
189.64
EC Number:
225-323-6
MDL number:
MFCD00012879
UNSPSC Code:
12352100
PubChem Substance ID:
24847145
NACRES:
NA.22

Quality Level

100

Assay

98%

form

solid

mp

162-164 °C (lit.)

SMILES string

Cl.NCC(O)c1cccc(O)c1

InChI

1S/C8H11NO2.ClH/c9-5-8(11)6-2-1-3-7(10)4-6;/h1-4,8,10-11H,5,9H2;1H

InChI key

OWMFSWZUAWKDRR-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Norphenylephrine hydrochloride was used in the study of the effects of phenylephrine on the isolated heart of rabbit.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

M Maeda et al.
International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 41(5), 463-469 (1990-01-01)
[11C]-p- and m-octopamine hydrochloride were synthesized from [11C]HCN in a two-step sequence. Chemical and enzymatic approaches were used for the formation of the [11C]cyanohydrin intermediates as the key step. Isolated radiochemical yields of 0.7-2.3% at the end-of-synthesis were obtained with
J C David et al.
Journal of neurochemistry, 53(1), 149-154 (1989-07-01)
Functions of octopamine in the mammalian brain are still not well known. An important aspect of this problem is the relationship between octopamines and catecholamines. Previous data have shown that their respective ontogenic evolutions are not parallel. Do the changes
L Jørgensen et al.
Urologia internationalis, 46(2), 176-179 (1991-01-01)
To study the acute effect of norfenefrine, given orally in aqueous solution, on the urethral closure function, profilometry was performed before and after administration of placebo and increasing doses of norfenefrine in 6 females with genuine stress incontinence. A weak
M R Gaab et al.
Advances in neurology, 52, 391-400 (1990-01-01)
We investigated the effects of the calcium entry blocker nimodipine on cerebral autoregulation, BBB, and vasogenic edema in animal experiments. In the first series of rats, ICBF was measured with H2 clearance using a balanced multiwire surface electrode. Variations in
R B Raffa et al.
European journal of pharmacology, 169(2-3), 317-320 (1989-10-10)
Administration of p-octopamine by intracerebroventricular (i.c.v.) or intrathecal (i.t.) routes, but not orally, produced antinociception in the acetylcholine-induced abdominal constriction test (ED50 = 24.8 and 3.6 micrograms, respectively). Likewise, i.c.v. and i.t., but not peripheral (up to 200 mg/kg s.c.)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service