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Dokumenty

45371

Supelco

Carboxine

PESTANAL®, analytical standard

Synonim(y):

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

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About This Item

Wzór empiryczny (zapis Hilla):
C12H13NO2S
Numer CAS:
5234-68-4
Masa cząsteczkowa:
235.30
Beilstein:
983249
Numer WE:
226-031-1
Numer MDL:
MFCD00055403
Kod UNSPSC:
41116107
Identyfikator substancji w PubChem:
329756679
NACRES:
NA.24

klasa czystości

analytical standard

Poziom jakości

100

linia produktu

PESTANAL®

okres trwałości

limited shelf life, expiry date on the label

metody

HPLC: suitable
gas chromatography (GC): suitable

Zastosowanie

agriculture
environmental

format

neat

ciąg SMILES

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

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)

Klucz InChI

GYSSRZJIHXQEHQ-UHFFFAOYSA-N

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Zastosowanie

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

Polecane produkty

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.

Informacje prawne

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
This page may contain text that has been machine translated.

Hasło ostrzegawcze

Warning

Zwroty wskazujące rodzaj zagrożenia

H302,H317,H373,H410

Zwroty wskazujące środki ostrożności

P260 - P273 - P280 - P301 + P312 - P302 + P352 - P314

Klasyfikacja zagrożeń

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

Organy docelowe

Kidney

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

212.0 °F - closed cup

Temperatura zapłonu (°C)

100 °C - closed cup

Środki ochrony indywidualnej

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

Choose from one of the most recent versions:

Certyfikaty analizy (CoA)

Lot/Batch Number
BCCL6938
BCCC3071
BCBT8120
BCBT3580
SZBG069XV

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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)
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
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
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.
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