AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D

AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D Structure
CAS No.
29611-03-8
Chemical Name:
AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D
Synonyms
afl;Ccris 11;flatoxicol;aflatoxicol;Aflatoxicol A;Einecs 249-727-7;[1S]-Aflatoxicol;aflatoxicolnaturalepimer;ahydro-1-hydroxy-4-methoxy-;aflatoxin R0, natural isomer
CBNumber:
CB5497906
Molecular Formula:
C17H14O6
Molecular Weight:
314.29
MOL File:
29611-03-8.mol
MSDS File:
SDS
Modify Date:
2023/6/8 9:02:47

AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D Properties

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

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06
Signal word  Danger
Hazard statements  H350-H360-H300+H310+H330-H319
Precautionary statements  P260-P280-P310
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
NFPA 704
0
4 0

AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D Chemical Properties,Uses,Production

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.

Chemical Properties

solid

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

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.

AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 34)Suppliers
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ATK CHEMICAL COMPANY LIMITED +undefined-21-51877795 China 32760 60 Inquiry
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MedChemExpress 021-58955995 United States 6398 58 Inquiry
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 China 11289 58 Inquiry
United States Biological 800.520.3011 or 781.639.5092 United States 6256 80 Inquiry
AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D afl aflatoxicol aflatoxicolnaturalepimer ahydro-1-hydroxy-4-methoxy- cyclopenta(c)furo(3’,2’:4,5)furo(2,3-h)(1)benzopyran-11(1h)-one,2,3,6a,9a-tetr [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 aflatoxin R0, natural isomer (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 (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 Ccris 11 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)- Einecs 249-727-7 Ccris 11/ Aflatoxin Ro/ Aflatoxicol [1S]-Aflatoxicol Aflatoxicol I natural isomer Aflatoxicol A flatoxicol 29611-03-8