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AFLATOXIN G2

CAS No.
7241-98-7
Chemical Name:
AFLATOXIN G2
Synonyms
AF G2;AFLATOXIN G2;AFLATOXIN G2(RG);Dihydroaflatoxin G1;AflatoxinG2,crystalline;Aflatoxin G2;Aflatoxin G2 0.5ug/ml in ACN;Aflatoxin G2 Solution, 3 Mg/L;10a-hexahydro-5-methoxy-1(7ar-cis)-;AFLATOXIN G2 FROM ASPERGILLUS FLAVUS
CBNumber:
CB3291098
Molecular Formula:
C17H14O7
Molecular Weight:
330.29
MDL Number:
MFCD00078141
MOL File:
7241-98-7.mol
Last updated:2023-06-08 09:01:59

AFLATOXIN G2 Properties

Melting point 237-240 °C
alpha D -473° (c = 0.084 in chloroform)
Boiling point 387.74°C (rough estimate)
Density 1.3099 (rough estimate)
refractive index 1.4790 (estimate)
Flash point 2 °C
storage temp. 2-8°C
solubility DMF: Soluble; DMSO: Soluble; Ethanol: Soluble; Methanol: Soluble
form White to yellow powder. Blue-green fluorescence.
Water Solubility 15mg/L(temperature not stated)
BRN 1692017
LogP 0.443 (est)
FDA UNII 2MS0D8WA29
EPA Substance Registry System Aflatoxin G2 (7241-98-7)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07,GHS08
Signal word  Danger
Hazard statements  H225-H304-H315-H319-H340-H350-H372-H412
Precautionary statements  P210-P273-P301+P310-P303+P361+P353-P305+P351+P338-P331
Hazard Codes  T+,T,Xn,F
Risk Statements  45-26/27/28-36-20/21/22-11-39/23/24/25-23/24/25-65-48/23/24/25-36/38-46
Safety Statements  53-28-36/37-45-36-26-16-7-62
RIDADR  UN 3462 6.1/PG 1
WGK Germany  3
RTECS  LV1700000
HazardClass  6.1(a)
PackingGroup  I
HS Code  30029090
Toxicity LD50 orally in day old duckling: 172.5 mg/50 gm body wt (Carnaghan)
NFPA 704
0
4 0

AFLATOXIN G2 price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich A0263 Aflatoxin G2 7241-98-7 1mg $228 2024-03-01 Buy
Sigma-Aldrich CRM46326 Aflatoxin G2 solution certifiedreferencematerial,3?μg/mLinbenzene:acetonitrile(98:2),ampuleof 7241-98-7 1mL $51.78 2024-03-01 Buy
Sigma-Aldrich 34033 Aflatoxin G2 solution 0.5?μg/mLinacetonitrile,analyticalstandard 7241-98-7 2ml $339 2024-03-01 Buy
Cayman Chemical 11296 Aflatoxin G2 ≥98% 7241-98-7 500μg $110 2024-03-01 Buy
Cayman Chemical 11296 Aflatoxin G2 ≥98% 7241-98-7 2.5mg $388 2024-03-01 Buy
Product number Packaging Price Buy
A0263 1mg $228 Buy
CRM46326 1mL $51.78 Buy
34033 2ml $339 Buy
11296 500μg $110 Buy
11296 2.5mg $388 Buy

AFLATOXIN G2 Chemical Properties,Uses,Production

Chemical Properties

The aflatoxins are a group of molds produced by the fungus Aspergillus flavus. They are natural contaminants of fruits, vegetables, and grains. They are also described as a series of condensed ring heterocyclic compounds. They form colorless to pale yellow crystals. Practically insoluble in water.

Chemical Properties

yellow powder

Uses

Aflatoxin G2 is the minor analogue of the green fluorescent family of bisfuranocoumarin mycotoxins produced by Aspergillus flavus and related species. Alfatoxins are one of the most potent mycotoxins known but are in fact "pre-toxins", requiring metabolic activation to the toxic principle. Aflatoxins are found widely in nature in trace amounts, particularly in grains and nuts. The toxicity of these metabolites was first recognised in the 1950s and their structures elucidated in 1963. Aflatoxins have been extensively reviewed.

Uses

Aflatoxins B1, B2, G1, G2 as secondary metabolites of fungal species such as Aspergillus flavus or Aspergillus parasiticus growing on a variety of foods (peanuts, nuts, spices, cereals). Aflatoxins are a group of very carcinogenic mycotoxins with hepatotoxic effects.

Definition

ChEBI: Aflatoxin G2 is a member of coumarins.

General Description

Very light and fluffy crystalline solid. Exhibits green-blue fluorescence.

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.

Biochem/physiol Actions

Hepatocarcinogen. Food contaminant produced by Aspergillus flavus, a common soil fungus.

Potential Exposure

Aflatoxins are a group of toxic metabolites produced by certain types of fungi. Aflatoxins are not commercially manufactured; they are naturally occurring contaminants that are formed by fungi on food during conditions of high temperatures and high humidity. Most human exposure to aflatoxins occurs through ingestion of contaminated food. The estimated amount of aflatoxins that Americans consume daily is estimated to be 0.15 0.50 μg. Grains, peanuts, tree nuts, and cottonseed meal are among the more common foods on which these fungi grow. Meat, eggs, milk, and other edible products from animals that consume aflatoxincontaminated feed may also contain aflatoxins. Aflatoxins can also be breathed in

Shipping

UN3172 Toxins, extracted from living sources, solid or liquid, Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required. UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

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.

Waste Disposal

Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal. Use of oxidizing agents, such as hydrogen peroxide or 5% sodium hypochlorite bleach. Acids and bases may also be used.

AFLATOXIN G2 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 122)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32686 60
Shanghai Zheyan Biotech Co., Ltd.
18017610038 zheyansh@163.com CHINA 3620 58
Chengdu GLP biotechnology Co Ltd
028-87075086 13350802083 scglp@glp-china.com CHINA 1824 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Hubei Ipure Biology Co., Ltd
+8613367258412 ada@ipurechemical.com China 10326 58
HONG KONG IPURE BIOLOGY CO.,LIMITED
86 18062405514 18062405514 ada@ipurechemical.com CHINA 3465 58
Finetech Industry Limited
+86-27-87465837 +8618971612321 info@finetechnology-ind.com China 9634 58
Hu Bei Jiutian Bio-medical Technology CO.,Ltd
027-88013699 17354350817 Ryan@jiutian-bio.com China 7433 58
Shanghai Acmec Biochemical Technology Co., Ltd.
+undefined18621343501 product@acmec-e.com China 33350 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 57511 58
)pyrano(3,4-c)(1)-benzopyran-1,12-dione 10a-hexahydro-5-methoxy-1(7ar-cis)- 12h-furo(3’,2’:4,5)furo(2,3-h)pyrano(3,4-c)(1)benzopyran-1,12-dione,3,4,7a-1 (7aR,cis)3,4,7a,9,10,10a-hexahydro-5-methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c]chromene-1,12-dione AF G2 AFLATOXIN G2(RG) (7aR)-3,4,7aα,9,10,10aα-Hexahydro-5-methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione 3,4,7aα,9,10,10aα-Hexahydro-5-methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione AFLATOXIN G(2) FROM ASPERGILLUS FLAVUS V IAL WITH 10 MG AFLATOXIN G2 FROM ASPERGILLUS FLAVUS AflatoxinG2,crystalline (7aR,10aS)-3,4,7a,9,10,10a-Hexahydro-5-Methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione Aflatoxin G2 Solution, 3 Mg/L 1h,12h-furo(3’,2’:4,5)furo(2,3-h)pyrano(3,4-c)(1)benzopyran-1,12-dione,3,4,7aa 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)- 1H,12H-Furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione, 3,4,7aalpha,9,10,10aalpha-hexahydro-5-methoxy- 3,4,7aalpha,9,10,10aalpha-hexahydro-5-methoxy-1h,12h-furo(3’,2’:4,5)furo(2,3-h 5-Methoxy-3,4,7a,9,10,10a-hexahydro-1H,12H-furo[3',2':4,5]furo[2,3-H]pyrano[3,4-c]chromene-1,12-dione 9,10,10a-alpha-hexahydro-5-methoxy-alph 9,10,10aalpha-hexahydro-5-methoxy-lph Dihydroaflatoxin G1 AFLATOXIN G2 Aflatoxin G2 Aflatoxin G2 (7aR,10aS)-3,4,7a,9,10,10a-Hexahydro-5-methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione (7aR,10aS)-5-methoxy-3,4,10,10a-tetrahydrofuro[3',2':4,5]furo[2,3-h]pyrano[3,4-c]chromene-1,12(7aH,9H)-dione Aflatoxin G2, 98%, from Aspergillus flavus 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,10aS)- Aflatoxin G2 0.5ug/ml in ACN Aflatoxin G2 solution in Acetonitrile, 100μg/mL (7aR,cis)3,4,7a,9,10,10a-hexahydro-5-methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c]chromene-1,12-dione 7241-98-7 7241-96-7 C17H14O7 BioChemical Cancer Research Carcinogens antibiotic CRM&Matrix RMApplication CRMs Food and Agriculture CRM Other CarcinogensCell Signaling and Neuroscience Cancer Research Mold Toxins and Venoms A AA to ALBiotoxins Alphabetic Mycotoxins Single component solutions Biotoxins Chiral Reagents Heterocycles Intermediates & Fine Chemicals Metabolites & Impurities Pharmaceuticals