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45349

Supelco

Bitertanol

PESTANAL®, analytical standard

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Synonym(s):
3,3-Dimethyl-1-(4-phenylphenoxy)-1-(1,2,4-triazol-1-yl)butan-2-ol
Empirical Formula (Hill Notation):
C20H23N3O2
CAS Number:
55179-31-2
Molecular Weight:
337.42
Beilstein:
620948
EC Number:
259-513-5
MDL number:
MFCD00055508
UNSPSC Code:
41116107
PubChem Substance ID:
329756665
NACRES:
NA.24

grade

analytical standard

Quality Level

100

description

mixture of stereo isomers

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

CC(C)(C)C(O)C(Oc1ccc(cc1)-c2ccccc2)n3cncn3

InChI

1S/C20H23N3O2/c1-20(2,3)18(24)19(23-14-21-13-22-23)25-17-11-9-16(10-12-17)15-7-5-4-6-8-15/h4-14,18-19,24H,1-3H3

InChI key

VGPIBGGRCVEHQZ-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.

Legal Information

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

WGK

WGK 2

Flash Point(F)

No data available

Flash Point(C)

No data available

Regulatory Information

农药列管产品

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’.

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Y Yamazaki et al.
Journal of AOAC International, 81(6), 1252-1256 (1998-12-16)
A simple and rapid method was developed for determining bitertanol residues in strawberries. Bitertanol was extracted from samples with ethyl acetate. Bitertanol acetate was added prior to extraction as a surrogate standard. The ethyl acetate extract was cleaned up by
Marc Bourgin et al.
Chemosphere, 90(4), 1387-1395 (2012-09-25)
The degradation of bitertanol by ozone treatment is investigated. Solutions of bitertanol (8.4 μg mL(-1)) were prepared either by dissolution of the standard or by dilution of Gaucho Blé seed loading solution and then ozonated under different conditions. Evolution of
Rafael Boscolo-Berto et al.
Legal medicine (Tokyo, Japan), 47, 101742-101742 (2020-07-13)
The fatal rupture of a saccular aneurysm at the junction between the left anterior cerebral artery and anterior communicating artery affected by fibromuscular dysplasia (FMD) is a rare condition. Here is reported the case of a subject involved in a
A R Allen et al.
Neurotoxicology and teratology, 15(4), 237-242 (1993-07-01)
Several recent reports indicate that triadimefon, a triazole fungicide, has effects on behavior that are similar to those of psychomotor stimulants. For example, triadimefon increases overall fixed-interval (FI) response rate, disrupts FI response patterning, increases motor activity, and produces stereotypies
Tatiana Zamora et al.
Journal of separation science, 27(9), 645-652 (2004-09-25)
Coupled-column liquid chromatography with fluorescence detection was applied to the determination of o-phenylphenol and bitertanol residues in orange and banana fruits. After extraction with a mixture of acetone, dichloromethane-petroleum ether, and ethyl acetate, an extract aliquot of 100 microL was
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