AFLATOXIN M1

AFLATOXIN M1 Basic information
Product Name:AFLATOXIN M1
Synonyms:38546, AFLATOXIN M STANDARD SOLUTIO;aflatoxin m1 solution;aflatoxin m1solution;ALFATOXINM1;AF M1;AF M1;Aflatoxin M1;4-Hydroxyaflatoxin B1;Aflatoxin M1 standard solution;2,3,6aα,9aα-Tetrahydro-9a-hydroxy-4-methoxycyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione
CAS:6795-23-9
MF:C17H12O7
MW:328.27
EINECS:229-865-4
Product Categories:mycosol;antibiotic;Heterocycles;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;Biotoxins;Mycotoxins;Single component solutions;A;AA to ALBiotoxins;Alphabetic;Cancer Research;Chiral Reagents;CarcinogensCell Signaling and Neuroscience;Mold;Toxins and Venoms
Mol File:6795-23-9.mol
AFLATOXIN M1 Structure
AFLATOXIN M1 Chemical Properties
Melting point 299℃
alpha D -280° (c = 0.1 in DMF)
Boiling point 386.03°C (rough estimate)
density 1.3358 (rough estimate)
refractive index 1.4790 (estimate)
Fp 11 °C
storage temp. 2-8°C
solubility Acetonitrile:Methanol (1:1): 1 mg/ml
form White to yellow powder.
pka10.76±0.20(Predicted)
BRN 1630643
Safety Information
Hazard Codes T+,T,F,Xn
Risk Statements 26/27/28-40-39/23/24/25-23/25-23/24/25-11-36-20/21/22-45
Safety Statements 53-22-36/37/39-45-24-16-7-36-26-36/37-28
RIDADR UN 3462 6.1/PG 1
WGK Germany 3
RTECS GY1880000
10-23
HazardClass 6.1(a)
PackingGroup I
HS Code 29322090
ToxicityLD50 orally in day old Pekin ducklings: 16.6 mg/duckling (Holzapfel, Steyn)
MSDS Information
ProviderLanguage
SigmaAldrich English
AFLATOXIN M1 Usage And Synthesis
Chemical PropertiesSolid
Chemical PropertiesThe 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.
UsesAn Aspergillus flavus metabolite. Aflatoxin M1 in milk as a secondary metabolite of the Aflatoxin B1 formed in moldy forages. It is cancerogenic, hepatotoxic, and immunosuppressive in animals and man.
DefinitionChEBI: A member of the class of aflatoxins that is aflatoxin B1 in which the hydrogen at position 9a is replaced by a hydroxy group.
General DescriptionCertan Vial
Safety ProfileConfirmed carcinogen with experimental tumorigenic data. Poison by ingestion. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes. See also various aflatoxins.
Potential ExposureAflatoxins 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
ShippingUN3172 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.
IncompatibilitiesIncompatible 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 DisposalConsult 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 M1 Preparation Products And Raw materials
4-Methyl-5,7-dimethoxycoumarin 5,7-Dihydroxy-4-methylcoumarin 5,7-Dimethoxycoumarin 1-Cyclopentenecarboxylic acid CHEMBRDG-BB 9070765 1'-hydroxyestragole AFLATOXIN M1, [3H(G)] 2-(Allyloxy)benzyl alcohol 2,3-Dihydrofuran 6-(4-HYDROXYPHENYL)HEXANOIC ACID Dimecrotic acid 7-HYDROXY-3,4,8-TRIMETHYLCOUMARIN (R)-1-PHENYL-2-PROPEN-1-OL Floverine 3-acetyl-8-allyl-2H-chromen-2-one 5 7-DIHYDROXY-4-PROPYLCOUMARIN 98 CHEMBRDG-BB 6367113 2,4,6-TRIMETHOXYBENZYL ALCOHOL

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