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140-56-7

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140-56-7 Usage

Description

Introduced in 1955, fenaminosulf (1; Lesan; Dexon) was one of the first selective, systemic fungicides. It is active against Phycomycetes such as Pythium, Phytophthora, and Aphanomyces but has little or no effect on higher fungi belonging to the Ascomycetes or Basidiomycetes. Fenaminosulf has a relatively high water solubility (20,000 mgL-1), a feature often associated with fungicides that specifically inhibit Oomycetes (3). Another important physicochemical property is photolytic instability, one of the reasons that fenaminosulf was developed as a seed dressing and soil fungicide (4). As a consequence of acute toxicity , limited spectrum, and photo-instability, the use of fenaminosulf decreased (4), and it is now listed in The Pesticide Manual (5) among products that have been superseded. Although no longer used, it is included here for completeness, being the only example of a commercial fungicide that acts on complex I. During its period of use, fenaminosulf, as wettable powder (WP), dust, or granular formulations, was employed as a seed dressing and soil-applied fungicide to control damping off and foot/root rots. Fenaminosulf-based products were used on a range of plants including vegetables, field crops, ornamentals, and turf.

Uses

Used in biological and pharmacological studies including:? ;Cloning and characterization of GABA transporter1? ;Activity of anti-RSV carbonucleosides2? ;Inhibition by fungicides of urea hydrolysis and nitrification of urea nitrogen in soil3

General Description

Yellow-brown crystals or brown powder.

Air & Water Reactions

Dust may form an explosive mixture in air. Water soluble.

Reactivity Profile

Aqueous solutions are sensitive to exposure to light.

Fire Hazard

Flash point data are not available for Fenaminosulf. Fenaminosulf is probably combustible.

Safety Profile

Poison by ingestion, intravenous, and intraperitoneal routes. Experimental teratogenic effects. Human mutation data reported. Questionable carcinogen, A fungicide. When heated to decomposition it emits very toxic fumes of NOx, Na2O, and SOx

Check Digit Verification of cas no

The CAS Registry Mumber 140-56-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 140-56:
(5*1)+(4*4)+(3*0)+(2*5)+(1*6)=37
37 % 10 = 7
So 140-56-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H11N3O3S/c1-11(2)8-5-3-7(4-6-8)9-10-15(12,13)14/h3-6H,1-2H3,(H,12,13,14)/p-1/b10-9+

140-56-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name fenaminosulf

1.2 Other means of identification

Product number -
Other names sodium (EZ)-4-dimethylaminobenzenediazosulfonate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Fungicide
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:140-56-7 SDS

140-56-7Upstream product

140-56-7Downstream Products

140-56-7Related news

Determination of genotoxicity of Fenaminosulf (cas 140-56-7) by Allium and Comet tests09/29/2019

Genotoxic effects of Fenaminosulf, fungicide and micro-biocide, were examined by using mitotic index (MI), mitotic phase, and Comet assay on the root meristem cells of Allium cepa. In the Allium root growth inhibition test, EC 50 value was firstly determined as 25ppm and, 12.5 (0.5×EC ...detailed

Selective detection of Fenaminosulf (cas 140-56-7) via a molecularly imprinted fluorescence switch and silver nano-film amplification10/01/2019

A novel fluorescence switch sensor was constructed for detecting the fungicide fenaminosulf (FM), based on a dye-doped molecularly imprinted polymer (MIP) and silver nanofilm amplification. The MIP was prepared by electropolymerization of hydroquinone doped with neutral red on the silver nanofil...detailed

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