Skip to Content
Merck
All Photos(1)

Documents

H-013

Supelco

Hexobarbital solution

1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C12H16N2O3
CAS Number:
Molecular Weight:
236.27
EC Number:
UNSPSC Code:
41116107
NACRES:
NA.24

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

technique(s)

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

application(s)

forensics and toxicology

format

single component solution

storage temp.

2-8°C

SMILES string

CN1C(=O)NC(=O)C(C)(C1=O)C2=CCCCC2

InChI

1S/C12H16N2O3/c1-12(8-6-4-3-5-7-8)9(15)13-11(17)14(2)10(12)16/h6H,3-5,7H2,1-2H3,(H,13,15,17)

InChI key

UYXAWHWODHRRMR-UHFFFAOYSA-N

General description

Hexobarbital is a hypnotic and a sedative and is sold under the trade names Citopan, Evipan, and Tobinal. This Snap-N-Spike® Reference Solution is applicable for use in applications including urine drug testing, clinical toxicology, and forensic analysis by LC-MS/MS or GC/MS.

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

Signal Word

Danger

Hazard Classifications

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

Target Organs

Eyes

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


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

Kenji Matsui et al.
PloS one, 7(4), e36433-e36433 (2012-05-05)
Almost all terrestrial plants produce green leaf volatiles (GLVs), consisting of six-carbon (C6) aldehydes, alcohols and their esters, after mechanical wounding. C6 aldehydes deter enemies, but C6 alcohols and esters are rather inert. In this study, we address why the
Markus Buchhaupt et al.
Applied microbiology and biotechnology, 93(1), 159-168 (2011-07-27)
Green notes are substances that characterize the aroma of freshly cut grass, cucumbers, green apples, and foliage. In plants, they are synthesized by conversion of linolenic or linoleic acid via the enzymes lipoxygenase (LOX) and hydroperoxide lyase (HPL) to short-chained
V G Lukashin et al.
Morfologiia (Saint Petersburg, Russia), 136(6), 48-52 (2009-01-01)
The effect of hexenal and nembutal on the tissue bushy receptors was studied the living isolated frog urinary bladder using methylene blue staining. These drugs were shown to induce the changes in the receptor pulse activity which included three phases:
V E Novikov et al.
Eksperimental'naia i klinicheskaia farmakologiia, 75(9), 7-10 (2012-11-20)
The influence of the new triazinoindole derivative encoded VM-606 on the individual behavior of rats in the open-field and elevated-plus-maze tests has been studied under normal conditions and after exposure to hypoxia with hypercapnia. It is established that VM-606 at
Peng-Ying Zhang et al.
Journal of integrative plant biology, 50(1), 84-91 (2008-08-01)
Volatiles emitted from the leaves of Lycopersicon esculentum at the two-, ten-leaf and anthesis periods were collected by a gas absorbing method and analyzed by gas chromatography (GC)-mass spectrometry. In total, 33 compounds of volatiles emitted from three developmental stage

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