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Safety Information

N-914

Supelco

Norethandrolone solution

1.0 mg/mL in 1,2-dimethoxyethane, ampule of 1 mL, certified reference material, Cerilliant®

Synonym(s):

Norethandrolone solution

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About This Item

Empirical Formula (Hill Notation):
C20H30O2
CAS Number:
52-78-8
Molecular Weight:
302.45
MDL number:
MFCD00198409
UNSPSC Code:
41116107
PubChem Substance ID:
329818611

grade

certified reference material

Quality Level

300

form

liquid

feature

Snap-N-Spike®/Snap-N-Shoot®

packaging

ampule of 1 mL

manufacturer/tradename

Cerilliant®

concentration

1.0 mg/mL in 1,2-dimethoxyethane

technique(s)

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

application(s)

pharmaceutical (small molecule)

format

single component solution

storage temp.

−20°C

SMILES string

CC[C@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]12C

InChI

1S/C20H30O2/c1-3-20(22)11-9-18-17-6-4-13-12-14(21)5-7-15(13)16(17)8-10-19(18,20)2/h12,15-18,22H,3-11H2,1-2H3/t15-,16+,17+,18-,19-,20-/m0/s1

InChI key

ZDHCJEIGTNNEMY-XGXHKTLJSA-N

General description

A certified solutionstandard applicable for use in sports testing, urine drug testing, or forensic analysis by LC-MS/MS or GC/MS. Norethandrolone is an anabolic androgenic steroid sold under the trade name Nilevar for the treatment of hormone deficiency, burns, trauma and anemia.

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

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Signal Word

Danger

Hazard Statements

H225,H315,H332,H360FD

Hazard Classifications

Acute Tox. 4 Inhalation - Flam. Liq. 2 - Repr. 1B - Skin Irrit. 2

Supplementary Hazards

EUH019

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

28.4 °F - closed cup

Flash Point(C)

-2 °C - closed cup

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PRTR

Class I Designated Chemical Substances

FSL

Group 4: Flammable liquids
Type 1 petroleums
Hazardous rank II
Water insoluble liquid

JAN Code

N-914-CC:
N-914-1ML:

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B Zumoff
Steroids, 53(1-2), 233-240 (1989-01-01)
Patients with diseases characterized by salt retention manifest a loss of the normal ability of healthy persons to escape from repeat injections of aldosterone or other salt-retaining steroids. This phenomenon may be a clue to the pathophysiological mechanisms of salt
M Claustres et al.
European journal of pediatrics, 144(5), 467-471 (1986-02-01)
The effects of natural and synthetic androgens on erythroid colony formation in children's bone marrow cultures were studied using a methylcellulose microculture assay. In an attempt to predict the clinical response to androgens in two children with Fanconi anaemia (FA)
B Frémond et al.
Chirurgie pediatrique, 28(2), 97-101 (1987-01-01)
The authors report 2 cases of hepatocellular tumour in children treated with anabolic androgens for aplastic anemia. In both cases, the presentation was by a picture of acute abdomen due to hemoperitoneum caused by tumour rupture. In the first case
M Van Puymbroeck et al.
Journal of chromatography. B, Biomedical sciences and applications, 728(2), 217-232 (1999-07-16)
The metabolism of the illegal growth promoter ethylestrenol (EES) was evaluated in bovine liver cells and subcellular fractions of bovine liver preparations. Incubations with bovine microsomal preparations revealed that EES is extensively biotransformed into norethandrolone (NE), another illegal growth promoter.
A R McKinney et al.
Journal of mass spectrometry : JMS, 36(2), 145-150 (2001-04-05)
After oral administration to a thoroughbred gelding, the anabolic steroid norethandrolone was converted into a complex mixture of oxygenated metabolites. These metabolites were extracted from the urine, deconjugated by methanolysis and converted to their O-methyloxime trimethylsilyl derivatives. Gas chromatographic/mass spectrometric
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