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AFLATOXIN G1

CAS No.1165-39-5
Chemical Name:AFLATOXIN G1
Synonyms:AF G1;AFLATOXIN G;AFLATOXIN G1;AFLATOXIN G1(RG);AF G1;Aflatoxin G1;aflatoxin g1solution;aflatoxin g1 solution;10a-tetrahydro-5-methoxy-;Aflatoxin G1, crystalline;(7ar-cis)-10a-tetrahydro-5-methoxy
CBNumber:CB4702106
Molecular Formula:C17H12O7
Formula Weight:328.27
MOL File:1165-39-5.mol
AFLATOXIN G1 Property
mp : 244-246 °C
Fp : -11 °C
storage temp. : 2-8°C
Safety
Hazard Codes : T+,T,F,Xn
Risk Statements : 45-26/27/28-65-48/23/24/25-36/38-11-46-39/23/24/25-23/24/25-36-20/21/22
Safety Statements : 53-28-36/37-45-62-26-16-7-36
RIDADR : UN 3462 6.1/PG 1
WGK Germany : 3
RTECS : LV1720000
F : 10
HazardClass : 6.1(a)
PackingGroup : I

AFLATOXIN G1 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 a re a group of very carcinogenic mycotoxins with hepatotoxic effects.
Usage
Aflatoxin G1 is the major 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 G1 is the major 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.
AFLATOXIN G1 Preparation Products And Raw materials
Raw materials
Preparation Products
AFLATOXIN G1 Suppliers      Global( 43)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
BEST-REAGENT 028-85973071 028-85973075028-85973075service@best-reagent.comCHINA 9961 57
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
 
1165-39-5(AFLATOXIN G1)Related Search:
7-HYDROXY-3-METHYL-2H-CHROMEN-2-ONE Phloroglucinol 5,7-DIHYDROXYCOUMARIN 4-Isopropylanisole Methyl tiglate DIMETHYL ETHYLIDENEMALONATE AFLATOXIN G1 ETHYL PHENYL MALONATE 1,3-DIETHOXYBENZENE 2-ALLYL-6-METHYLPHENOL ETHYL CROTONATE Aflatoxin ETHYL COUMARIN-3-CARBOXYLATE 3,4-DIMETHYL-CHROMEN-2-ONE 2-METHOXYSTYRENE 2-HYDROXYCINNAMALDEHYDE 2-PROPENYLPHENOL 2-methylpent-2-en-1-ol
BioChemical Carcinogens 1165-39-5 Cancer Research AFLATOXIN G AFLATOXIN G1 (7ar-cis)-10a-tetrahydro-5-methoxy 10a-tetrahydro-5-methoxy- 1h,12h-furo(3’,2’:4,5)furo(2,3-h)pyrano(3,4-c)(1)benzopyran-1,12-dione,3,4,7a, 1H,12H-Furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione, 3,4,7a,10a-tetrahydro-5-methoxy-, (7aR-cis)- 5-Methoxy-3,4,7a,10a-tetrahydro-1H,12H-furo[3',2':4,5]furo[2,3-H]pyrano[3,4-c]chromene-1,12-dione (7aR,cis)3,4,7a,10a-tetrahydro-5-methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c]chromene-1,12-dione AF G1 AF G1;Aflatoxin G1 AFLATOXIN G1 FROM ASPERGILLUS FLAVUS AFLATOXIN G(1) FROM ASPERGILLUS FLAVUS VIAL WITH 10 MG* Aflatoxin G1, crystalline C17H12O7 aflatoxin g1 solution aflatoxin g1solution AFLATOXIN G1(RG) 32827 Biotoxins Mycotoxins Single component solutions CRM&Matrix RMApplication CRMs Food and Agriculture CRM Other A AA to ALBiotoxins Alphabetic Cancer Research CarcinogensCell Signaling and Neuroscience Mold Toxins and Venoms (7aR)-3,4,7aα,10aα-Tetrahydro-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,10aα-Tetrahydro-5-methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione 5-Methoxy-3,4,7aα,10aα-tetrahydro-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione 1h,12h-Furo[3',2':4,5]Furo[2,3-H]Pyrano[3,4-C][1]Benzopyran-1,12-Dione, 3,4,7a,10a-Tetrahy Chiral Reagents Heterocycles Intermediates & Fine Chemicals Metabolites & Impurities Pharmaceuticals (7aR,10aS)-3,4,7a,10a-Tetrahydro-5-Methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione antibiotic Aflatoxin G1 (7aR,10aS)-3,4,7a,10a-Tetrahydro-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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