Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

N-057

Supelco

Noratropine hydrochloride solution

1.0 mg/mL in methanol (as free base), ampule of 1 mL, certified reference material, Cerilliant®

Synonym(s):

Noratropine hydrochloride

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

About This Item

Empirical Formula (Hill Notation):
C16H21NO3·HCl
CAS Number:
537-29-1
Molecular Weight:
311.80
EC Number:
200-659-6
UNSPSC Code:
41116107

grade

certified reference material

form

liquid

feature

Snap-N-Spike®/Snap-N-Shoot®

packaging

ampule of 1 mL

manufacturer/tradename

Cerilliant®

concentration

1.0 mg/mL in methanol (as free base)

technique(s)

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

application(s)

pharmaceutical (small molecule)

format

single component solution

storage temp.

−20°C

InChI

1S/C16H21NO3.ClH/c18-10-15(11-4-2-1-3-5-11)16(19)20-14-8-12-6-7-13(9-14)17-12;/h1-5,12-15,17-18H,6-10H2;1H/t12-,13-,15?;/m1./s1

InChI key

JBSGQNAULGFCJE-JAWPBFRBSA-N

General description

The primary metabolite of atropine, an anticholinergic drug used in opthalmology, resuscitation from cardiac arrest, and treatment for organophosphate poisoning. A Certified Solution Standard for use in LC or GC applications.

Legal Information

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

related product

Product No.
Description
Pricing

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

49.5 °F - closed cup

Flash Point(C)

9.7 °C - closed cup

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support.

Already Own This Product?

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

Visit the Document Library

Preparation of noratropine by oxidative n-demethylation of atropine.
M J Van der Meer et al.
The Journal of pharmacy and pharmacology, 35(6), 408-408 (1983-06-01)
Mohamad Houssam Al Balkhi et al.
Phytochemistry, 74, 105-114 (2011-11-16)
The presence of two compounds, norlittorine and norhyoscyamine, has been reported in leaves and roots of Datura innoxia; however their metabolic origin in the tropane alkaloid pathway has remained unknown. Precise knowledge of this pathway is a necessary pre-requisite to
M J Van der Meer et al.
The Journal of pharmacy and pharmacology, 38(10), 781-784 (1986-10-01)
A metabolic pattern of atropine in man, based on the detection of radiolabelled products in urine by high performance liquid chromatography after administration of [3H]atropine sulphate to a normal volunteer is proposed. Noratropine (24%), atropine-N-oxide (equatorial isomer) (15%), tropine (2%)

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