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AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D

CAS No.
29611-03-8
Chemical Name:
AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D
Synonyms
aflatoxicol;afl;Ccris 11;flatoxicol;Aflatoxicol A;[1S]-Aflatoxicol;Einecs 249-727-7;aflatoxicolnaturalepimer;ahydro-1-hydroxy-4-methoxy-;aflatoxin R0, natural isomer
CBNumber:
CB5497906
Molecular Formula:
C17H14O6
Molecular Weight:
314.29
MDL Number:
MFCD00082506
MOL File:
29611-03-8.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 03:44:45

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.
color White to off-white
Stability Hygroscopic
EWG's Food Scores 1
FDA UNII 45I1K5482V

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
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 price More Price(15)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 20437 Aflatoxin R0 ≥98% 29611-03-8 1mg $601 2026-04-30 Buy
Usbiological 441041 Aflatoxicol 29611-03-8 500ug $807 2026-06-03 Buy
Usbiological 441041 Aflatoxicol 29611-03-8 1mg $1557 2026-06-03 Buy
Biosynth BA162706 Aflatoxicol 29611-03-8 1mg $1476.96 2026-06-04 Buy
Biosynth BA162706 Aflatoxicol 29611-03-8 5mg $6277.05 2026-06-04 Buy
Product number Packaging Price Buy
20437 1mg $601 Buy
441041 500ug $807 Buy
441041 1mg $1557 Buy
BA162706 1mg $1476.96 Buy
BA162706 5mg $6277.05 Buy

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

Chemical Properties

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

Aflatoxicol is a reduction metabolite of Aflatoxin B1 (A357460), which is a potent environmental mutagen and carcinogen.

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.

References

[1] M NAKAZATO. Interconversion of aflatoxin B1 and aflatoxicol by several fungi.[J]. Applied and Environmental Microbiology, 1990, 56 5: 1465-1470. DOI: 10.1128/aem.56.5.1465-1470.1990
[2] J J WONG  D P H. Mutagenicity of aflatoxins related to their metabolism and carcinogenic potential.[J]. Proceedings of the National Academy of Sciences of the United States of America, 1976, 73 7: 2241-2244. DOI: 10.1073/pnas.73.7.2241

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

Raw materials

Preparation Products

Global Suppliers ( 41)
Supplier Tel Email Country ProdList Advantage
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9799 58
Qingdao IniKem BioPharmaTech Co.,Ltd 0532-58268781 18561687109 sales@inikem.com China 298 55
Shanghai Hongye Biotechnology Co. Ltd 400-9205774 400-920-5774 sales@glpbio.cn China 6705 58
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 sales@rrkchem.com China 57336 58
TargetMol Chemicals Inc. +1-781-999-5354; +1-00000000000 marketing@targetmol.com United States 32431 58
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11123 58
Shaanxi Dideu Medichem Co. Ltd 029-81154043 17391733319 1086@dideu.com China 9970 58
Shanghai Hewu Biotechnology Co., LTD 021-57886085 17317861055 shhebio@126.com CHINA 7971 58
Nanjing Shizhou Biology Technology Co.,Ltd 025-85560043 13675144456 sean.lv@synzest.com China 11432 58
Aflatoxicol A Ccris 11/ Aflatoxin Ro/ Aflatoxicol [1S]-Aflatoxicol Aflatoxicol I natural isomer AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D 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 flatoxicol Aflatoxin R0 / Aflatoxicol I (natural isomer) afl aflatoxicol 29611-03-8