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Aflatoxin G2 is a secondary metabolite of fungal species such as Aspergillus flavus or Aspergillus parasiticus, which can grow on a variety of foods including peanuts, nuts, spices, and cereals. It belongs to the group of very carcinogenic mycotoxins with hepatotoxic effects. Aflatoxin G2 is the minor analogue of the green fluorescent family of bisfuranocoumarin mycotoxins. Although aflatoxins are one of the most potent mycotoxins known, they are "pre-toxins" that require metabolic activation to become toxic. Aflatoxins are found widely in nature in trace amounts, particularly in grains and nuts. The toxicity of these metabolites was first recognized in the 1950s, and their structures were elucidated in 1963.

7241-98-7

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7241-98-7 Usage

Uses

Aflatoxin G2 does not have any direct applications due to its toxic nature. However, it is important to be aware of its presence in food products and take necessary precautions to prevent contamination and exposure. The detection and monitoring of aflatoxin levels in food products are crucial to ensure food safety and protect public health. Various analytical methods, such as chromatography and immunoassays, are employed to detect and quantify aflatoxin levels in food samples. Additionally, research is being conducted to develop strategies for reducing aflatoxin contamination in crops and food products, such as using resistant crop varieties, proper storage conditions, and biological control agents.

Air & Water Reactions

Slightly water soluble

Reactivity Profile

AFLATOXIN G2 is incompatible with strong oxidizing agents, strong acids and strong bases.

Health Hazard

ACUTE/CHRONIC HAZARDS: AFLATOXIN G2 is extremely toxic. Ingestion of even microgram quantities can cause toxic affects and, possibly, death. It can also be absorbed through the skin. Allow only your most experienced personnel to work with AFLATOXIN G2. All non-essential personnel should leave the laboratory.

Fire Hazard

Flash point data for AFLATOXIN G2 are not available. AFLATOXIN G2 is probably combustible.

Incompatibilities

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides.

Check Digit Verification of cas no

The CAS Registry Mumber 7241-98-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,4 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7241-98:
(6*7)+(5*2)+(4*4)+(3*1)+(2*9)+(1*8)=97
97 % 10 = 7
So 7241-98-7 is a valid CAS Registry Number.

7241-98-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name AFLATOXIN G2

1.2 Other means of identification

Product number -
Other names 1H,12H-Furo[3‘,2‘:4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione, 3,4,7a,9,10,10a-hexahydro-5-methoxy-, (7aR-cis)-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:7241-98-7 SDS

7241-98-7Upstream product

7241-98-7Downstream Products

7241-98-7Relevant academic research and scientific papers

Kinetic and mechanistic investigations on reductions of aflatoxins by lactic acid

Shukla, Ram S.,Verma, Ramtej J.,Mehta, Daxa N.

, p. 2737 - 2741 (2007/10/03)

The kinetics of reduction of AFB1 to AFB2 and AFG1 to AFG2 by lactic acid has been investigated in dilute aqueous acidic solutions (pH 3.35-4.50) as a function of the concentrations of lactic acid, AFB1, AFG1 and hydrogen ion at 37°C. The rate of the reaction was found to be first order with respect to the concentrations of lactic acid and aflatoxins and independent on hydrogen ion concentration. The experimental results are interpreted in terms of mechanisms involving an initial formation of transient oxonium intermediate, which tends to polarize the olefinic (C=C) carbon, which in turn causes the hydride abstraction from α-carbon atom of lactic acid in rate determining step. The proposed mechanisms involve an overall transfer of two protons and two electrons from lactic acid to AFB1 and AFG1 to give the corresponding reduced less toxic products AFB2 and AFG2 and the oxidised product pyruvic acid.

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