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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;Aflatoxin G2;AflatoxinG2,crystalline;Aflatoxin G2 Solution, 3 Mg/L;10a-hexahydro-5-methoxy-1(7ar-cis)-;AFLATOXIN G2 FROM ASPERGILLUS FLAVUS;9,10,10aalpha-hexahydro-5-methoxy-lph
CBNumber:CB3291098
Molecular Formula:C17H14O7
Formula Weight:330.29
MOL File:7241-98-7.mol
AFLATOXIN G2 Property
mp : 237-240 °C
Fp : 2 °C
storage temp. : 2-8°C
Safety
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

AFLATOXIN G2 Chemical Properties,Usage,Production

Chemical Properties
yellow powder
Usage
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.
Usage
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.
Usage
Aflatoxin G2 is the minor analogue of the green fluorescent family of bisfuranocoumarin mycotoxins produced by Aspergillus flavus and related species. Aflatoxins 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.
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.
AFLATOXIN G2 Preparation Products And Raw materials
Raw materials
Preparation Products
AFLATOXIN G2 Suppliers      Global( 38)Suppliers     
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J & K SCIENTIFIC LTD. ----jkinfo@jkchemical.com;market3@jkchemical.comCHINA 96847 76
JinYan Chemicals(ShangHai) Co.,Ltd. 13817811078,021-5042603086-021-50426522,50426273sales@jingyan-chemical.comCHINA 10108 60
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.comCHINA 32553 50
Dalian Meilun Biotech Co., Ltd. 0411-66771943;0411-667719420411-66771945sales@meilune.comCHINA 5010 58
ShangHai YuanYe Biotechnology Co., Ltd. 021-61312847 qq:2797782341021-601373572797782341@qq.comCHINA 7597 60
Cheng Du Micxy Chemical Co.,Ltd 028-85632863 028-64559668 18048500443028-85632863 QQ: 2509670926micxysales@163.comCHINA 13240 58
Shanghai Tauto Biotech Co., Ltd 0086-21-513205880086-21-51320502export2@tautobiotech.comCHINA 4011 66
Clearsynth Labs Limited +91-22-26355700 +91-22-26355701info@clearsynth.comINDIA 9914 58
ChemStrong Scientific Co.,Ltd 0755 668533660755 28363542sales@chem-strong.com;CHINA 11269 56
Shanghai Aspire Biological Technology Co., Ltd. 021-61317773021-61486878sales@aspirebio.comCHINA 4812 58
 
7241-98-7(AFLATOXIN G2)Related Search:
2-PROPENOIC ACID, 3-(4-ETHOXYPHENYL)-, METHYL ESTER trans-2,3-Dimethoxycinnamic acid 3-Methylphenethyl alcohol 3,4-DIMETHYL-CHROMEN-2-ONE (2E)-3-(2,3-DIHYDROBENZOFURAN-5-YL)PROPENOICACID 7-METHOXY-2H-CHROMENE-3-CARBOXYLIC ACID ETHYL ESTER 3-(4-BUTOXYPHENYL)-2-PROPENOIC ACID ETHYL PHENYL MALONATE AFLATOXIN G2 5,6-DIHYDRO-2H-PYRAN-3-CARBOXYLIC ACID 4-Methoxycinnamic acid 7-HYDROXY-2-OXO-2H-CHROMENE-3-CARBOXYLIC ACID METHYL ESTER 3-Phenoxypropionic acid 3,5-DIPROPOXYPHENOL 7-HYDROXY-3,4,8-TRIMETHYLCOUMARIN 5,6-dihydro-2H-pyran-3-carbaldehyde 2-(4-methoxy-3-methylphenyl)ethanol 2-METHOXYHYDROCINNAMIC ACID
)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 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 7241-98-7 BioChemical Cancer Research Carcinogens Aflatoxin G2 (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 G(2) FROM ASPERGILLUS FLAVUS V IAL WITH 10 MG AFLATOXIN G2 FROM ASPERGILLUS FLAVUS AflatoxinG2,crystalline C17H14O7 AFLATOXIN G2(RG) 7241-96-7 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 (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 Chiral Reagents Heterocycles Intermediates & Fine Chemicals Metabolites & Impurities Pharmaceuticals (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 antibiotic 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
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