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AFLATOXIN B1

AFLATOXIN B1 Structure
CAS No.
1162-65-8
Chemical Name:
AFLATOXIN B1
Synonyms
afb1;AFLATOXIN B;AFBI;AflatoxinB1(form1);aflatoxin b1solution;Aflatoxin B1, 98%, from Aspergillus flavus;Aflatoxin B1 Solution in Acetonitrile, 100μg/mL;HSDB 3453;NSC 529592;alflatoxin
CBNumber:
CB5389650
Molecular Formula:
C17H12O6
Molecular Weight:
312.27
MOL File:
1162-65-8.mol
Modify Date:
2024/7/2 8:55:11

AFLATOXIN B1 Properties

Melting point 268-269 °C
alpha D -558° (c = 0.1 in CHCl3); D -480° (c = 0.1 in DMF)
Boiling point 372.21°C (rough estimate)
Density 1.2810 (rough estimate)
refractive index 1.4800 (estimate)
Flash point 2 °C
storage temp. 2-8°C
solubility DMF: 20 mg/ml; DMF:PBS(pH 7.2)(1:1): 0.5 mg/ml; DMSO: 12 mg/ml
form White to yellow powder.
color White to yellow
Water Solubility 15mg/L(temperature not stated)
Merck 13,180
BRN 1269174
Stability Stable. Incompatible with strong oxidizing agents. May be light or air sensitive.
InChIKey OQIQSTLJSLGHID-WNWIJWBNSA-N
LogP 2.039 (est)
EPA Substance Registry System Aflatoxin B1 (1162-65-8)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06,GHS08
Signal word  Danger
Hazard statements  H300+H310+H330-H340-H350-H361
Precautionary statements  P201-P262-P280-P301+P310+P330-P302+P352+P310-P304+P340+P310
Hazard Codes  T+,T,Xn,F
Risk Statements  45-46-26/27/28-36-20/21/22-11-65-48/23/24/25-36/38-39/23/24/25-23/24/25
Safety Statements  53-45-36-26-16-24-7-62-36/37-28
RIDADR  UN 3462 6.1/PG 1
WGK Germany  3
RTECS  GY1925000
10
HazardClass  6.1(a)
PackingGroup  I
HS Code  29322090
Toxicity LD50 orally in day old duckling: 18.2 mg/50 gm body wt (Carnaghan); i.p. in newborn mice: 9.50 mg/kg body wt (Büchi)
NFPA 704
0
4 0

AFLATOXIN B1 price More Price(7)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) A6636 Aflatoxin B1 from Aspergillus flavus from Aspergillus flavus 1162-65-8 1MG ₹6191.9 2022-06-14 Buy
Sigma-Aldrich(India) A6636 Aflatoxin B1 from Aspergillus flavus from Aspergillus flavus 1162-65-8 5MG ₹20231.93 2022-06-14 Buy
Sigma-Aldrich(India) CRM46323 Aflatoxin B1 solution certified reference material, 3?μg/mL in benzene:acetonitrile (98:2), ampule of 1?mL 1162-65-8 1ML ₹7288.4 2022-06-14 Buy
Sigma-Aldrich(India) A6636 Aflatoxin B1 from Aspergillus flavus from Aspergillus flavus 1162-65-8 10MG ₹33958.03 2022-06-14 Buy
Sigma-Aldrich(India) A6636 Aflatoxin B1 from Aspergillus flavus from Aspergillus flavus 1162-65-8 50MG ₹112428.45 2022-06-14 Buy
Product number Packaging Price Buy
A6636 1MG ₹6191.9 Buy
A6636 5MG ₹20231.93 Buy
CRM46323 1ML ₹7288.4 Buy
A6636 10MG ₹33958.03 Buy
A6636 50MG ₹112428.45 Buy

AFLATOXIN B1 Chemical Properties,Uses,Production

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

Aflatoxin B1 is the major analogue of a family of bisfuranocoumarin mycotoxins produced by Aspergillus flavus and related species. Aflatoxin B1 exhibits a distinctive UV spectrum and blue fluorescence. Aflatoxins are among the most potent mycotoxins known but are in fact "pre-toxins", requiring metabolic activation to the toxic principle. Aflatoxins are found widely in nature in trace amounts, particularly in grains and nuts. The toxicity of these metabolites was first recognised in the 1950s and their structures elucidated in 1963. Aflatoxins have been extensively reviewed.

Definition

ChEBI: An aflatoxin having a tetrahydrocyclopenta[c]furo[3',2':4,5]furo[2,3-h]chromene skeleton with oxygen functionality at positions 1, 4 and 11.

General Description

Colorless to pale yellow crystals or white powder. Exhibits blue fluorescence.

Air & Water Reactions

Sensitive to exposure to air and light. Water insoluble.

Reactivity Profile

AFLATOXIN B1 is incompatible with strong oxidizing agents, strong acids and strong bases.

Fire Hazard

Flash point data for AFLATOXIN B1 are not available; however, AFLATOXIN B1 is probably combustible.

Safety Profile

Confirmed human carcinogen with experimental tumorigenic, neoplas tigenic, and carcinogenic data. Acute poison by ingestion, intraperitoneal, and possibly other routes. Experimental teratogenic and reproductive effects. Mutation data reported. When heated to decomposition it emits acrid smoke. 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

Metabolic pathway

Aflatoxin B1 can be activated via the monooxygenase reaction which then reacts with the N7 atom of B-DNA guanine. Conjugation of aflatoxin B1 8,9-epoxide is an important detoxification route. Although aflatoxin B1 8,9-epoxide can be hydrolyzed to the diol by epoxide hydrolase, the diol product is toxic, since it reacts readily with proteins by Schiff base formation or binds to DNA. Glutathione conjugation prevents toxicity of both the epoxide and its hydrolysis product. The aflatoxin glutathione conjugate is subsequently excreted from the hepatocyte into bile as a major biliary metabolite.

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.

AFLATOXIN B1 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 196)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
Alfa Aesar 1 800 209 7001 Maharashtra, India 6913 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
SynZeal Research Pvt Ltd +1 226-802-2078 Gujarat, India 6522 58 Inquiry
Pharma Affiliates 172-5066494 Haryana, India 6761 58 Inquiry
Hebei Mojin Biotechnology Co., Ltd +86 13288715578 +8613288715578 China 12459 58 Inquiry
Henan Fengda Chemical Co., Ltd +86-371-86557731 +86-13613820652 China 20361 58 Inquiry
Hangzhou FandaChem Co.,Ltd. 008657128800458; +8615858145714 China 9338 55 Inquiry
ATK CHEMICAL COMPANY LIMITED +undefined-21-51877795 China 32760 60 Inquiry
Chengdu GLP biotechnology Co Ltd 028-87075086 13350802083 CHINA 1824 58 Inquiry
(6ar-cis)-ahydro-4-methoxy )(1)benzopyran-1,11-dione 1-Cyclopentene-1-carboxylic acid, 2-(3a,8a-dihydro-4-hydroxy-6-methoxyfuro[2,3-b]benzofuran-5-yl)-5-oxo-, delta-lactone 2,3,6aalpha,9aalpha-tetrahydro-4-methoxycyclopenta(c)furo(3’,2’:4,5)furo(2,3-h 4-Methoxy-2,3,6a,9a-tetrahydrocyclopenta[c]furo[3',2':4,5]furo[2,3-H]chromene-1,11-dione 2,3,6aalpha,9aalpha-tetrahydro-4-methoxycyclopenta[c]furo[2',3':4,5]furo[2,3-h]chromene-1,11-dione AFLATOXIN B1 FROM ASPERGILLUS FLAVUS AFLATOXIN B(1) FROM ASPERGILLUS FLAVUS, VIAL WITH 10 MG Aflatoxin B1, crystalline (6aR)-4-Methoxy-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-methoxycyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione (6aR,9aS)-2,3,6a,9a-Tetrahydro-4-Methoxy-1H,11H-cyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione NSC 529592 Aflaloxin B1 aflatoxin b1 solution AFLATOXIN B1(RG) Aflatoxin FB1, Aflatoxin B cyclopenta(c)furo(3’,2’:4,5)furo(2,3-h)(1)benzopyran-1,11-dione,2,3,6a,9a-tet cyclopenta(c)furo(3’,2’:4,5)furo(2,3-h)(1)benzopyran-1,11-dione,2,3,6a,9a-tetr cyclopenta(c)furo(3’,2’:4,5)furo(2,3-h)(1)benzopyran-1,11-dione,2,3,6aalpha,9a Cyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione, 2,3,6a,9a-tetrahydro-4-methoxy-, (6aR-cis)- Cyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione, 2,3,6aalpha,9aalpha-tetrahydro-4-methoxy- rahydro-4-methoxy- AFLATOXIN B1 AFLATOXIN B1, ASPERGILLUS FLAVUS 1H,11H-Cyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione,2,3,6a,9a-tetrahydro-4-Methoxy-, (6aR,9aS)- 6-methoxydifurocoumarone ahydro-4-methoxy- alflatoxin alflatoxinb1 alpha-tetrahydro-4-methoxy- Cyclopenta(c)furo(3',2':4,5)furo(2,3-h)(1)benzopyran-1,11-dione, 2,3,6a,9a-tetrahydro-4-methoxy- Standard Solution Aflatoxin B1 Aflatoxin B1 Standard (6aR,9aS)-4-methoxy-2,3-dihydrocyclopenta[c]furo[3',2':4,5]furo[2,3-h]chromene-1,11(6aH,9aH)-dione Cyclopenta[c]furo[3'',2'':4,5]furo[2,3-h][1]benzopyran-1,11-dione,2,3,6a,9a-tetrahydro-4-methoxy-, (6aR,9aS)- AflatoxinB1Solution,3mg/L AflatoxinB1Solution,10mg/L Aflatoxin B1 2ug/ml in ACN Aflatoxin B1 Solution in Acetonitrile, 10μg/mL Aflatoxin B1 Solution in Methanol, 100μg/mL Aflatoxin B1-13C10 11-methoxy-6,8,19-trioxapentacyclo[10.7.0.02,.03,.013,1]nonadeca-1,4,9,11,13(17)-pentaene-16,18-dione aflatoxin b1solution AFLATOXIN B afb1 AFBI AflatoxinB1(form1) Aflatoxin B1, 98%, from Aspergillus flavus Aflatoxin B1 Solution in Acetonitrile, 100μg/mL Aflatoxin B1/BSA Aflatoxin B1/KLH HSDB 3453 Aflatoxin Quality Control Sample,From corn 1162-65-8 C17H12O6 BioChemical Carcinogens