32215-02-4

Basic information

• Product Name: AFLATOXIN P1
• Synonyms: AFLATOXIN P1;(6ar-cis)-rahydro-4-hydroxy;AFP1;(6aR)-4-Hydroxy-2,3,6aα,9aα-tetrahydrocyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione;2,3,6aα,9aα-Tetrahydro-4-hydroxycyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione;Cyclopenta(C)furo(3',2':4,5)furo(2,3-H)(1)-benzopyran-1,11-dione, 2,3,6A,9A-tetrahydro-4-hydroxy-, (6ar,9as)-;Cyclopenta(C)furo(3',2':4,5)furo(2,3-H)(1)-benzopyran-1,11-dione, 2,3,6A,9A-tetrahydro-4-hydroxy-, (6ar-cis)-;(6aR,9aS)-2,3,6a,9a-Tetrahydro-4-hydroxycyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione
• CAS NO: 32215-02-4
• Molecular Formula: C16H10O6
• Molecular Weight: 298.249
• Product Categories: Chiral Reagents;Heterocycles;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;Chiral Reagents, Heterocycles, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 32215-02-4.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 544.5 °C at 760 mmHg
• Flash Point: 211.9 °C
• Appearance: /
• Density: 1.7 g/cm³
• Vapor Pressure: 1.81E-12mmHg at 25°C
• Refractive Index: 1.75
• Storage Temp.: 2-8°C
• PKA: 7.05±0.20(Predicted)
• CAS DataBase Reference: AFLATOXIN P1(CAS DataBase Reference)
• NIST Chemistry Reference: AFLATOXIN P1(32215-02-4)
• EPA Substance Registry System: AFLATOXIN P1(32215-02-4)

Safety Data

• Hazard Codes: T+
• Statements: 45-46-26/27/28
• Safety Statements: 53-22-36/37/39-45
• RIDADR: UN 2811 6.1/PG 1
• WGK Germany: 3
• RTECS: GY1775000
• HazardClass: 6.1(a)
• PackingGroup: I
• Hazardous Substances Data: 32215-02-4(Hazardous Substances Data)

Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 32215-02-4 differently. You can refer to the following data:
1. Pale Yellow Solid
2. 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.

Uses

The oxidative metabolite of Aflatoxin B1; shows the highest risck of hepatocellular carcinoma.

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.

InChI:InChI=1/C16H10O6/c17-8-2-1-6-11-9(18)5-10-13(7-3-4-20-16(7)21-10)14(11)22-15(19)12(6)8/h3-5,7,16,18H,1-2H2/t7-,16+/m0/s1