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46174

Diaveridine

VETRANAL®, analytical standard

Synonym(s):

5-(3,4-Dimethoxybenzyl)-2,4-pyrimidinediamine

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About This Item

Empirical Formula (Hill Notation):
C13H16N4O2
CAS Number:
5355-16-8
Molecular Weight:
260.29
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329757094
EC Number:
226-333-3
Beilstein/REAXYS Number:
258464
MDL number:
MFCD00057349
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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)

clinical testing

format

neat

storage temp.

2-8°C

SMILES string

COc1ccc(Cc2cnc(N)nc2N)cc1OC

InChI

1S/C13H16N4O2/c1-18-10-4-3-8(6-11(10)19-2)5-9-7-16-13(15)17-12(9)14/h3-4,6-7H,5H2,1-2H3,(H4,14,15,16,17)

InChI key

LDBTVAXGKYIFHO-UHFFFAOYSA-N

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Application

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

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 2

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC9436

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A Tanabe et al.
Nihon yakurigaku zasshi. Folia pharmacologica Japonica, 86(6), 411-415 (1985-12-01)
The preventive effect of sulfaquinoxaline and diaveridine in combination against leucocytozoon infection in White Leghorn female chickens was tested in a field trial. The experiment was initiated when the animals were 120 days old, and it lasted for 10 weeks.
Tomoko Ono-Ogata et al.
Environmental and molecular mutagenesis, 39(1), 43-48 (2002-01-29)
We examined the mutagenic activities of six antiprotozoal drugs (three diaminopyrimidine compounds [pyrimethamine, diaveridine, and trimethoprim] and three 8-aminoquinoline derivatives [primaquine, pentaquine, and pamaquine]) in Escherichia coli WP2uvrA/pKM101 and Salmonella typhimurium TA100 and TA98 with and without nitrite treatment. The
P Tömpe et al.
Acta pharmaceutica Hungarica, 60(1), 23-29 (1990-01-01)
Differential pulse polarographic method was applied for determination of diaveridine in plasma, whole blood and isolated organs (liver, spleen, kidney, thymus). Deproteinization of homogenized blood and organs had been carried out on Extrelut column and then concentration of diaveridine was
Determination of residual diaveridine and sulfaquinoxaline in Hen's egg, chicken plasma and tissues by high-performance liquid chromatography.
T Sakano et al.
Chemical & pharmaceutical bulletin, 29(8), 2290-2295 (1981-08-01)
G Gigler et al.
Agents and actions. Supplements, 32, 39-43 (1991-01-01)
The compound EGIS-5645 is a potent antipyretic agent possessing analgesic and antiinflammatory properties. The drug is active in antiinflammatory models such as carrageenin oedema and adjuvant arthritis. EGIS-5645 shows practically no gastro-ulcerogenic effect. The molecule does not inhibit either prostaglandin
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