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Merck
CN

45904

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
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329757009
EC Number:
200-835-2
Beilstein/REAXYS Number:
611817
MDL number:
MFCD00128025

Key Documents

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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

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

Regulatory Information

危险化学品

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Certificates of Analysis (COA)

Lot/Batch Number
BCBS8836V

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Hua Chen et al.
Analytical chemistry, 81(10), 4010-4014 (2009-04-23)
This paper presents the first membrane inlet method that can be used together with field portable mass spectrometers for the analysis of semivolatile pharmaceuticals (pethidine, benzophenone, and cocaine) and environmental pollutants (terbutryne and butylated hydroxyl toluene (BHT)) dissolved in organic
K Marja Talja et al.
Journal of agricultural and food chemistry, 56(24), 11962-11968 (2008-12-05)
The degradation of pesticides atrazine and terbutryn was investigated under aerobic and anaerobic conditions in the northern boreal region subsurface deposits and sterilized controls from the depths of 6.3-21.0 m below the surface and 1.2-16.9 m below the groundwater table.
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
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
Andrea Ventrella et al.
Biosensors & bioelectronics, 26(12), 4747-4752 (2011-06-21)
In this study, ultrathin film multilayers of Photosystem II-enriched photosynthetic membranes (BBY) were prepared and immobilized on quartz substrates by means of a Layer by Layer procedure exploiting electrostatic interactions with poly(ethylenimine) as polyelectrolyte. The biomaterials thus obtained were characterized
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