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AFLATOXIN G1

CAS No.
1165-39-5
Chemical Name:
AFLATOXIN G1
Synonyms
AF G1;AFLATOXIN G;AFLATOXIN G1;AFLATOXIN G1(RG);AF G1;Aflatoxin G1;aflatoxin g1solution;aflatoxin g1 solution;10a-tetrahydro-5-methoxy-;Aflatoxin G1, crystalline;AflatoxinG1Solution,3mg/L
CBNumber:
CB4702106
Molecular Formula:
C17H12O7
Molecular Weight:
328.27
MDL Number:
MFCD28143303
MOL File:
1165-39-5.mol
MSDS File:
SDS
Last updated:2023-06-08 09:01:59

AFLATOXIN G1 Properties

Melting point 244-246 °C
alpha D -556° (chloroform)
Boiling point 386.03°C (rough estimate)
Density 1.3358 (rough estimate)
refractive index 1.4790 (estimate)
Flash point -11 °C
storage temp. 2-8°C
solubility DMF: Soluble; DMSO: Soluble; Ethanol: Soluble; Methanol: Soluble
Water Solubility 15mg/L(temperature not stated)
BRN 1299768
LogP 0.679 (est)
FDA UNII 1DB78J7PUD
EPA Substance Registry System Aflatoxin G1 (1165-39-5)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07,GHS08
Signal word  Danger
Hazard statements  H225-H304-H315-H319-H340-H350-H372-H412
Precautionary statements  P210-P273-P301+P310-P303+P361+P353-P305+P351+P338-P331
Hazard Codes  T+,T,F,Xn
Risk Statements  45-26/27/28-65-48/23/24/25-36/38-11-46-39/23/24/25-23/24/25-36-20/21/22
Safety Statements  53-28-36/37-45-62-26-16-7-36
RIDADR  UN 3462 6.1/PG 1
WGK Germany  3
RTECS  LV1720000
10
HazardClass  6.1(a)
PackingGroup  I
HS Code  29322090
Toxicity LD50 orally in day old duckling: 39.2 mg/50 gm body wt (Carnaghan)
NFPA 704
0
4 0

AFLATOXIN G1 price More Price(18)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich CRM46325 Aflatoxin G1 solution certified reference material, 3?μg/mL in benzene:acetonitrile (98:2), ampule of 1?mL 1165-39-5 1mL $51.78 2024-03-01 Buy
Sigma-Aldrich 34032 Aflatoxin G1 solution 2?μg/mL in acetonitrile, analytical standard 1165-39-5 2ml $339 2024-03-01 Buy
Sigma-Aldrich 32756 Aflatoxin G1 reference material 1165-39-5 5mg $2080 2024-03-01 Buy
Cayman Chemical 11295 Aflatoxin G1 ≥98% 1165-39-5 1mg $93 2024-03-01 Buy
Cayman Chemical 11295 Aflatoxin G1 ≥98% 1165-39-5 5mg $275 2024-03-01 Buy
Product number Packaging Price Buy
CRM46325 1mL $51.78 Buy
34032 2ml $339 Buy
32756 5mg $2080 Buy
11295 1mg $93 Buy
11295 5mg $275 Buy

AFLATOXIN G1 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.

Chemical Properties

yellow powder

Uses

Aflatoxin G1 from Aspergillus flavus has been used as a standard for the determination of aflatoxin in various samples.

Uses

Aflatoxin G1 is the major analogue of the green fluorescent family of bisfuranocoumarin mycotoxins produced by Aspergillus flavus and related species. Alfatoxins are one of 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.

Uses

Aflatoxins B1, B2, G1, G2 as secondary metabolites of fungal species such as Aspergillus flavus or Aspergillus parasiticus growing on a variety of foods (peanuts, nuts, spices, cereals). Aflatoxins a re a group of very carcinogenic mycotoxins with hepatotoxic effects.

Definition

ChEBI: Aflatoxin G is a member of coumarins.

General Description

Certan Vial

Biochem/physiol Actions

Hepatocarcinogen. Food contaminant produced by Aspergillus flavus, a common soil fungus.

Safety Profile

Confirmed human carcinogen with experimental carcinogenic and neoplastigenic data. Poison by ingestion and intraperitoneal routes. 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.

AFLATOXIN G1 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 133)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
Shanghai Zheyan Biotech Co., Ltd.
18017610038 zheyansh@163.com CHINA 3620 58
Chengdu GLP biotechnology Co Ltd
028-87075086 13350802083 scglp@glp-china.com CHINA 1824 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
Finetech Industry Limited
+86-27-87465837 +8618971612321 info@finetechnology-ind.com China 9702 58
TargetMol Chemicals Inc.
+1-781-999-5354 support@targetmol.com United States 19973 58
LEAPCHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 43348 58
Shanghai Acmec Biochemical Technology Co., Ltd.
+undefined18621343501 product@acmec-e.com China 33349 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 57511 58
Qingdao IniKem BioPharmaTech Co.,Ltd 18561687109 sales@inikem.com China 287 55

View Lastest Price from AFLATOXIN G1 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Aflatoxin G1 pictures 2020-02-11 Aflatoxin G1
1165-39-5
US $9.80 / KG 1g >98% 20 tons Career Henan Chemical Co
  • Aflatoxin G1 pictures
  • Aflatoxin G1
    1165-39-5
  • US $9.80 / KG
  • >98%
  • Career Henan Chemical Co
(7ar-cis)-10a-tetrahydro-5-methoxy 10a-tetrahydro-5-methoxy- 1h,12h-furo(3’,2’:4,5)furo(2,3-h)pyrano(3,4-c)(1)benzopyran-1,12-dione,3,4,7a, 1H,12H-Furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione, 3,4,7a,10a-tetrahydro-5-methoxy-, (7aR-cis)- 5-Methoxy-3,4,7a,10a-tetrahydro-1H,12H-furo[3',2':4,5]furo[2,3-H]pyrano[3,4-c]chromene-1,12-dione AFLATOXIN G AFLATOXIN G1 Aflatoxin G1 (7aR,10aS)-3,4,7a,10a-Tetrahydro-5-methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione (7aR,cis)3,4,7a,10a-tetrahydro-5-methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c]chromene-1,12-dione AF G1 AF G1;Aflatoxin G1 AFLATOXIN G1 FROM ASPERGILLUS FLAVUS AFLATOXIN G(1) FROM ASPERGILLUS FLAVUS VIAL WITH 10 MG* Aflatoxin G1, crystalline aflatoxin g1 solution aflatoxin g1solution AFLATOXIN G1(RG) (7aR)-3,4,7aα,10aα-Tetrahydro-5-methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione 3,4,7aα,10aα-Tetrahydro-5-methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione 5-Methoxy-3,4,7aα,10aα-tetrahydro-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione 1h,12h-Furo[3',2':4,5]Furo[2,3-H]Pyrano[3,4-C][1]Benzopyran-1,12-Dione, 3,4,7a,10a-Tetrahy (7aR,10aS)-3,4,7a,10a-Tetrahydro-5-Methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione 5-methoxy-3,4-dihydrofuro[3',2':4,5]furo[2,3-h]pyrano[3,4-c]chromene-1,12(7aH,10aH)-dione Aflatoxin G1, 98%, from Aspergillus flavus AflatoxinG1Solution,3mg/L 1H,12H-Furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c][1]benzopyran-1,12-dione,3,4,7a,10a-tetrahydro-5-methoxy-, (7aR,10aS)- Aflatoxin G1 2ug/ml in ACN Aflatoxin G1 Solution in Acetonitrile, 100μg/mL Aflatoxin G1 Solution in Acetonitrile, 10μg/mL (7aR,cis)3,4,7a,10a-tetrahydro-5-methoxy-1H,12H-furo[3',2':4,5]furo[2,3-h]pyrano[3,4-c]chromene-1,12-dione Aflatoxin Quality Control Sample,From wheat 1165-39-5 C17H12O7 32827 Cancer Research BioChemical Carcinogens antibiotic Chiral Reagents Heterocycles Intermediates & Fine Chemicals Metabolites & Impurities Pharmaceuticals Biotoxins Mycotoxins Single component solutions CRM&Matrix RMApplication CRMs Food and Agriculture CRM Other A AA to ALBiotoxins Alphabetic Cancer Research CarcinogensCell Signaling and Neuroscience Mold Toxins and Venoms