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76547

Supelco

Isoprothiolane

PESTANAL®, analytical standard

Synonym(s):

Diisopropyl 2-(1,3-dithiolan-2-ylidene)malonate

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About This Item

Empirical Formula (Hill Notation):
C12H18O4S2
CAS Number:
50512-35-1
Molecular Weight:
290.40
Beilstein:
2128528
MDL number:
MFCD00210314
UNSPSC Code:
41116107
PubChem Substance ID:
329767175
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

Assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

storage temp.

2-8°C

SMILES string

CC(C)OC(=O)\C(C(=O)OC(C)C)=C1/SCCS1

InChI

1S/C12H18O4S2/c1-7(2)15-10(13)9(11(14)16-8(3)4)12-17-5-6-18-12/h7-8H,5-6H2,1-4H3

InChI key

UFHLMYOGRXOCSL-UHFFFAOYSA-N

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General description

Isoprothiolane is a systemic fungicide, which is used in controlling diseases rice stem rot, rice blast and Fusarium leaf spot on rice. Its mode of action basically involves the inhibition of penetration and elongation of infecting hyphae via inhibiting the formation of infecting peg or cellulose secretion.

Application

Isoprothiolane may be used as a reference standard in the determination of isoprothiolane in food samples using gas chromatography coupled with mass spectrometry (GC-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Legal Information

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PRTR

Class I Designated Chemical Substances

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

76547-50MG:4548174002858
76547-BULK:
76547-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL2323
BCCG2837
BCCC2968
BCBV1779
BCBT0671

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Z Feleke et al.
Water science and technology : a journal of the International Association on Water Pollution Research, 43(11), 25-33 (2001-07-11)
Biological denitrification and trace pesticide removal in a combined biofilm-electrode reactor/adsorption process has been investigated. In long-term (more than 260 days) continuous experiments, influent and effluent concentrations of nitrate, nitrite, isoprothiolane and gas composition were measured at different electric current
H Katamoto et al.
Nihon juigaku zasshi. The Japanese journal of veterinary science, 52(6), 1189-1197 (1990-12-01)
To study effects of isoprothiolane and phytosterol on dietary fat necrosis, 3 groups of rats were fed hardened-tallow (HT) diet. Two groups of rats received either isoprothiolane (50 mg/kg) or phytosterol (20 mg/kg) orally once a day consecutively for 10
Suneet Mittal et al.
Journal of cardiovascular electrophysiology, 13(4), 342-346 (2002-05-30)
Two randomized trials (Multicenter Automatic Defibrillator Implantation Trial [MADIT] and Multicenter Unsustained Tachycardia Trial [MUSTT]) suggest that implantable cardioverter defibrillator (ICD) placement is associated with improved survival in patients with coronary artery disease, depressed left ventricular function, and nonsustained ventricular
H Okada et al.
The Journal of veterinary medical science, 61(5), 553-556 (1999-06-24)
This study was performed to investigate the effects of isoprothiolane on cell growth and the production of interleukin (IL)-1 and IL-6 by bovine mammary epithelial cells in vitro. Isoprothiolane increased proliferation of mammary epithelial cells in a dose-dependent manner at
Y Ishida et al.
Physiology & behavior, 60(2), 633-638 (1996-08-01)
Responses of three chemical senses, olfaction, taste, and pit organ sense, to three pesticides were studied electrophysiologically in carp, Cyprinus carpio. Only olfaction was responsive to the three pesticides at behavioral avoidance levels, which were determined in a previous study.
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