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46468

Supelco

Monensin sodium salt hydrate

VETRANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C36H61NaO11 · xH2O
CAS Number:
22373-78-0
Molecular Weight:
692.85 (anhydrous basis)
EC Number:
244-941-7
UNSPSC Code:
41116107
E Number:
E714
NACRES:
NA.24

grade

analytical standard

Quality Level

200

product line

VETRANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

cleaning products
clinical
cosmetics
food and beverages
forensics and toxicology
personal care
pharmaceutical (small molecule)

format

neat

Mode of action

cell membrane | interferes

storage temp.

2-8°C

SMILES string

O.[Na+].CC[C@]1(CC[C@@H](O1)[C@]2(C)CC[C@]3(C[C@H](O)[C@@H](C)[C@H](O3)[C@@H](C)[C@@H](OC)[C@H](C)C([O-])=O)O2)[C@@H]4O[C@@H](C[C@@H]4C)[C@H]5OC(O)(CO)[C@H](C)C[C@@H]5C

InChI

1S/C36H62O11.Na/c1-10-34(31-20(3)16-26(43-31)28-19(2)15-21(4)36(41,18-37)46-28)12-11-27(44-34)33(8)13-14-35(47-33)17-25(38)22(5)30(45-35)23(6)29(42-9)24(7)32(39)40;/h19-31,37-38,41H,10-18H2,1-9H3,(H,39,40);/q;+1/p-1/t19-,20-,21+,22+,23-,24-,25-,26+,27+,28-,29+,30-,31+,33-,34-,35+,36-;/m0./s1

InChI key

XOIQMTLWECTKJL-FBZUZRIGSA-M

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General description

Chemical structure: polyether

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Statements

H300,H319,H373,H411

Hazard Classifications

Acute Tox. 2 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - STOT RE 2

Target Organs

Heart,muscle

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK2725
BCCH3805
BCCG4771
BCBT8654
BCBR9717V

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Sharon Cohen et al.
Molecular immunology, 54(2), 115-121 (2012-12-27)
It has been recently demonstrated that while oligosaccharide moieties of μ heavy chains in the B-cell receptor (BCR) are of the complex type as expected, those of the pre-BCR on the surface of pre-B cells contain oligosaccharide moieties of the
T L Felix et al.
Journal of animal science, 90(11), 3905-3913 (2012-06-06)
Two experiments were conducted to evaluate the effects of monensin and dried distillers grains with solubles (DDGS) on ruminal metabolism in 8 fistulated steers. In Exp. 1, treatments were (DM basis): 1) 0 mg monensin/kg diet DM, 2) 22 mg
Katia Soto-Liebe et al.
Toxicon : official journal of the International Society on Toxinology, 60(7), 1324-1334 (2012-09-18)
Paralytic shellfish poisoning (PSP) toxins are a group of naturally occurring neurotoxic alkaloids produced among several genera of primarily freshwater cyanobacteria and marine dinoflagellates. Although saxitoxin (STX) and analogs are all potent Na(+) channel blockers in vertebrate cells, the functional
T F Duffield et al.
Journal of animal science, 90(12), 4583-4592 (2012-08-04)
A meta-analysis of the impact of monensin on growing and finishing beef cattle was conducted after a search of the literature. A total of 40 peer-reviewed articles and 24 additional trial reports with monensin feeding in beef cattle were selected
Subbarao V Ravva et al.
PloS one, 8(1), e54782-e54782 (2013-01-26)
Surviving predation is a fitness trait of Escherichia coli O157:H7 (EcO157) that provides ample time for the pathogen to be transported from reservoirs (e.g. dairies and feedlots) to farm produce grown in proximity. Ionophore dietary supplements that inhibit rumen protozoa
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