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45904

Supelco

Terbutryn solution

100 μg/mL in acetonitrile, PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C10H19N5S
CAS Number:
886-50-0
Molecular Weight:
241.36
Beilstein/REAXYS Number:
611817
EC Number:
200-835-2
MDL number:
MFCD00128025
UNSPSC Code:
41116107
PubChem Substance ID:
329757009
NACRES:
NA.24

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

concentration

100 μg/mL in acetonitrile

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture

format

single component solution

storage temp.

2-8°C

SMILES string

CCNc1nc(NC(C)(C)C)nc(SC)n1

InChI

1S/C10H19N5S/c1-6-11-7-12-8(15-10(2,3)4)14-9(13-7)16-5/h6H2,1-5H3,(H2,11,12,13,14,15)

InChI key

IROINLKCQGIITA-UHFFFAOYSA-N

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

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

35.6 °F - closed cup

flash_point_c

2 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCBS8836V

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Carmen Rioboo et al.
Aquatic toxicology (Amsterdam, Netherlands), 94(3), 229-237 (2009-08-15)
Very little is known about growth and proliferation in relation to the cell cycle regulation of algae. The lack of knowledge is even greater when referring to the potential toxic effects of pollutants on microalgal cell division. To assess the
J Velisek et al.
Ecotoxicology and environmental safety, 73(3), 384-390 (2009-11-13)
The sub-chronic effects of terbutryn at concentrations 0.02 (reported concentration in Czech rivers), 4, 20, and 40 microg L(-1) were assessed in one-year-old common carp (Cyprinus carpio L.) exposed for 28 days and compared to a non-treated control group. Its
K Zimmermann et al.
Biochimica et biophysica acta, 1757(2), 106-114 (2006-02-14)
Binding of herbicides to photosystem II inhibits the electron transfer from Q(A) to Q(B) due to competition of herbicides with plastoquinone bound at the Q(B) site. We investigated herbicide binding to monomeric and dimeric photosystem II core complexes (PSIIcc) isolated
C Rioboo et al.
Aquatic toxicology (Amsterdam, Netherlands), 83(4), 247-253 (2007-06-08)
Few data exist on potential toxic effects that pollutants may have on zooplankton fed microalgae exposed to pesticides. For that reason, microalgal cultures were exposed to different concentrations of the triazine herbicide terbutryn, and used as exclusive food source to
C Fufezan et al.
Biochemistry, 44(15), 5931-5939 (2005-04-13)
To gain new insights into the function of photosystem II (PSII) herbicides DCMU (a urea herbicide) and bromoxynil (a phenolic herbicide), we have studied their effects in a better understood system, the bacterial photosynthetic reaction center of the terbutryn-resistant mutant
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