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AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D

Product Name
AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D
CAS No.
29611-03-8
Chemical Name
AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D
Synonyms
afl;Ccris 11;flatoxicol;aflatoxicol;Aflatoxicol A;[1S]-Aflatoxicol;Einecs 249-727-7;aflatoxicolnaturalepimer;ahydro-1-hydroxy-4-methoxy-;Aflatoxicol I natural isomer
CBNumber
CB5497906
Molecular Formula
C17H14O6
Formula Weight
314.29
MOL File
29611-03-8.mol
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AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D Property

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
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Safety

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
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H319Causes serious eye irritation

H350May cause cancer

H360May damage fertility or the unborn child

Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P310Immediately call a POISON CENTER or doctor/physician.

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N-Bromosuccinimide Price

Cayman Chemical
Product number
20437
Product name
Aflatoxin R0
Purity
≥98%
Packaging
1mg
Price
$546
Updated
2024/03/01
Apolloscientific
Product number
BIA4321
Product name
Aflatoxicol
Packaging
1mg
Price
$573
Updated
2021/12/16
AK Scientific
Product number
8341AJ
Product name
Aflatoxicol
Packaging
1mg
Price
$706
Updated
2021/12/16
Apolloscientific
Product number
BIA4321
Product name
Aflatoxicol
Packaging
100ug
Price
$116
Updated
2021/12/16
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AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D Chemical Properties,Usage,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.

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

Raw materials

Preparation Products

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AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE D Suppliers

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9709
Advantage
58
Shanghai Hongye Biotechnology Co. Ltd
Tel
400-9205774
Email
sales@glpbio.cn
Country
China
ProdList
6870
Advantage
58
Shenzhen Polymeri Biochemical Technology Co., Ltd.
Tel
+86-400-002-6226 13028896684
Email
sales@rrkchem.com
Country
China
ProdList
55896
Advantage
58
BOC Sciences
Tel
+16314854226
Email
inquiry@bocsci.com
Country
United States
ProdList
19743
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
19892
Advantage
58
Hubei Jusheng Technology Co.,Ltd.
Tel
18871490254
Fax
027-59599243
Email
linda@hubeijusheng.com
Country
CHINA
ProdList
28180
Advantage
58
ChemeGen(Shanghai) Biotechnology Co.,Ltd.
Tel
18818260767
Fax
QQ 3610331285
Email
sales@chemegen.com
Country
China
ProdList
11289
Advantage
58
Shaanxi Dideu Medichem Co. Ltd
Tel
029-61856359 18690052321
Fax
029-88380327
Email
1027@dideu.com
Country
China
ProdList
10008
Advantage
58
Shanghai Hewu Biotechnology Co., LTD
Tel
021-57886085 17317861055
Email
shhebio@126.com
Country
CHINA
ProdList
7975
Advantage
58

29611-03-8, AFLATOXICOL I NATURAL ISOMER*VACUUM DRIE DRelated Search:


  • Aflatoxicol A
  • Ccris 11/ Aflatoxin Ro/ Aflatoxicol
  • [1S]-Aflatoxicol
  • Aflatoxicol I natural isomer
  • 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
  • flatoxicol
  • 29611-03-8