| Identification | Back Directory | [Name]
AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D | [CAS]
29611-03-8 | [Synonyms]
afl
Ccris 11
flatoxicol
aflatoxicol
Aflatoxicol A
[1S]-Aflatoxicol
Einecs 249-727-7
aflatoxicolnaturalepimer
ahydro-1-hydroxy-4-methoxy-
Aflatoxicol I natural isomer
aflatoxin R0, natural isomer
AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D
Ccris 11/ Aflatoxin Ro/ Aflatoxicol
cyclopenta(c)furo(3’,2’:4,5)furo(2,3-h)(1)benzopyran-11(1h)-one,2,3,6a,9a-tetr
(1S)-2,3,6aα,9aα-Tetrahydro-1β-hydroxy-4-methoxycyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-11(1H)-one
Cyclopenta(C)furo(3',2':4,5)furo(2,3-H)(1)benzopyran-11(1H)-one, 2,3,6A,9A-tetrahydro-1-hydroxy-4-methoxy-, (1S,6ar,9as)-
(1S-(1alpha,6Abeta,9abeta))-2,3,6A,9A-tetrahydro-1-hydroxy-4-methoxycyclopenta(C)furo(3',2':4,5)furo(2,3-H)(1)benzopyran-11(1H)-one
[1S-(1alpha,6abeta,9abeta)]-2,3,6a,9a-tetrahydro-1-hydroxy-4-methoxycyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-11(1H)-one | [EINECS(EC#)]
249-727-7 | [Molecular Formula]
C17H14O6 | [MDL Number]
MFCD00082506 | [MOL File]
29611-03-8.mol | [Molecular Weight]
314.289 |
| Chemical Properties | Back Directory | [Appearance]
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. | [Melting point ]
225°C | [Boiling point ]
373.98°C (rough estimate) | [density ]
1.2564 (rough estimate) | [refractive index ]
1.4800 (estimate) | [storage temp. ]
2-8°C | [solubility ]
Methanol: 1 mg/ml | [form ]
White powder. | [Stability:]
Hygroscopic |
| Hazard Information | Back Directory | [Chemical Properties]
solid | [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 | [First aid]
Move victim to fresh air. Call 911 or emergency medical service. Give artificial respiration if victim is not breathing. Do not use mouth-to-mouth method if victim ingested or inhaled the substance; give artificial respiration with the aid of a pocket mask equipped with a one-way valve or other proper respiratory medical device. Administer oxygen if breathing is difficult. Remove and isolate contaminated clothing and shoes. In case of contact with substance, immediately flush skin or eyes with running water for at least 20 minutes. For minor skin contact, avoid spreading material on unaffected skin. Keep victim warm and quiet. Effects of exposure (inhalation, ingestion or skin contact) to substance may be delayed. Ensure that medical personnel are aware of the material(s) involved and take precautions to protect themselves. Medical observation is recommended for 24 to 48 hours after breathing overexposure, as pulmonary edema may be delayed. Asfirst aid for pulmonary edema, a doctor or authorized paramedic may consider administering a drug or other inhalation therapy
| [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.
| [Description]
Aflatoxin R0 is a metabolite of the carcinogenic mycotoxin aflatoxin B1 . Aflatoxin R0 is produced by metabolism in animals as well as in fungi and can be reverted to the parent compound in fungi. Aflatoxin R0 is highly mutagenic when tested in the Ames'' in vitro microbial detection system for carcinogens. | [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. | [Uses]
Aflatoxicol is a reduction metabolite of Aflatoxin B1 (A357460), which is a potent environmental mutagen and carcinogen. |
| Safety Data | Back Directory | [Hazard Codes ]
T+ | [Risk Statements ]
45-46-61-26/27/28 | [Safety Statements ]
53-22-36/37/39-45 | [RIDADR ]
3172 | [HazardClass ]
6.1(a) | [PackingGroup ]
I | [HS Code ]
29419090 | [Safety Profile]
Suspected carcinogen with experimental carcinogenic data. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes. See also various aflatoxins |
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