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Merck
CN

45371

Carboxine

PESTANAL®, analytical standard

Synonym(s):

5,6-Dihydro-2-methyl-N-phenyl-1,4-oxathiin-3-carboxamide, Carbathiine

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About This Item

Empirical Formula (Hill Notation):
C12H13NO2S
CAS Number:
5234-68-4
Molecular Weight:
235.30
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756679
EC Number:
226-031-1
Beilstein/REAXYS Number:
983249
MDL number:
MFCD00055403

Key Documents

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InChI key

GYSSRZJIHXQEHQ-UHFFFAOYSA-N

InChI

1S/C12H13NO2S/c1-9-11(16-8-7-15-9)12(14)13-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,13,14)

SMILES string

CC1=C(SCCO1)C(=O)Nc2ccccc2

grade

analytical standard

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

Quality Level

100

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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

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

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Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1 - STOT RE 2

target_organs

Kidney

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

212.0 °F - closed cup

flash_point_c

100 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCN3693
BCCL6938
BCCC3071
BCBT8120
BCBT3580

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Marina DellaGreca et al.
Journal of agricultural and food chemistry, 52(20), 6228-6232 (2004-09-30)
Sunlight exposure of aqueous suspensions of carboxin (1) causes its phototransformation to sulfoxide 2 and minor components. Similar effects are observed in the presence of humic acid or nitrate or at different pH values. Photoproducts 2-9 were isolated by chromatographic
Yoko Shima et al.
Fungal genetics and biology : FG & B, 46(1), 67-76 (2008-11-11)
Mutants exhibiting resistance to the fungicide, carboxin, were isolated from Aspergillus oryzae, and the mutations in the three gene loci, which encode succinate dehydrogenase (SDH) B, C, and D subunits, were identified to be independently responsible for the resistance. A
Tore Brinck et al.
Journal of molecular modeling, 9(2), 77-83 (2003-04-23)
We have recently shown that the anti-HIV activities of reverse transcriptase inhibitors can be related quantitatively to properties of the electrostatic potentials on their molecular surfaces. We now introduce the technique of using only segments of the drug molecules in
Lars Hederstedt
Biochimica et biophysica acta, 1553(1-2), 74-83 (2002-01-23)
An overview of the present knowledge about succinate:quinone oxidoreductase in Paracoccus denitrificans and Bacillus subtilis is presented. P. denitrificans contains a monoheme succinate:ubiquinone oxidoreductase that is similar to that of mammalian mitochondria with respect to composition and sensitivity to carboxin.
Yanshen Deng et al.
Toxicon : official journal of the International Society on Toxinology, 42(4), 351-357 (2003-09-25)
The effect of surangin B, an insecticidal natural product coumarin, on presynaptic release of endogenous amino acids was investigated using a purified synaptosomal fraction isolated from mouse brain. Surangin B stimulated the release of glutamic acid (GLU), gamma-aminobutyric acid (GABA)
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