AFLATOXIN G1

ChemicalBook > CAS DataBase List > AFLATOXIN G1

Product Name: 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;AFLATOXIN G1(RG) 10mg;10a-tetrahydro-5-methoxy-;Aflatoxin G1, crystalline
CBNumber: CB4702106
Molecular Formula: C17H12O7
Formula Weight: 328.27
MOL File: 1165-39-5.mol

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AFLATOXIN G1 Property

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
form: Solid
color: White to off-white
Water Solubility: 15mg/L(temperature not stated)
BRN: 1299768
LogP: 0.679 (est)
EPA Substance Registry System: Aflatoxin G1 (1165-39-5)

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Safety

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
F: 10
HazardClass: 6.1(a)
PackingGroup: I
HS Code: 29322090
Hazardous Substances Data: 1165-39-5(Hazardous Substances Data)
Toxicity: LD50 orally in day old duckling: 39.2 mg/50 gm body wt (Carnaghan)

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H225Highly Flammable liquid and vapour

H304May be fatal if swallowed and enters airways

H315Causes skin irritation

H319Causes serious eye irritation

H340May cause genetic defects

H350May cause cancer

H372Causes damage to organs through prolonged or repeated exposure

H412Harmful to aquatic life with long lasting effects

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P273Avoid release to the environment.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P331Do NOT induce vomiting.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: CRM46325
Product name: Aflatoxin G1 solution
Purity: certified reference material, 3?μg/mL in benzene:acetonitrile (98:2), ampule of 1?mL
Packaging: 1mL
Price: $51.78
Updated: 2024/03/01

Sigma-Aldrich

Product number: 34032
Product name: Aflatoxin G1 solution
Purity: 2?μg/mL in acetonitrile, analytical standard
Packaging: 2ml
Price: $339
Updated: 2024/03/01

Sigma-Aldrich

Product number: 32756
Product name: Aflatoxin G1
Purity: reference material
Packaging: 5mg
Price: $2080
Updated: 2024/03/01

Cayman Chemical

Product number: 11295
Product name: Aflatoxin G1
Purity: ≥98%
Packaging: 1mg
Price: $93
Updated: 2024/03/01

Cayman Chemical

Product number: 11295
Product name: Aflatoxin G1
Purity: ≥98%
Packaging: 5mg
Price: $275
Updated: 2024/03/01

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AFLATOXIN G1 Chemical Properties,Usage,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 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

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

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

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View Lastest Price from AFLATOXIN G1 manufacturers

Shaanxi Dideu Medichem Co. Ltd

Product: AFLATOXIN G1 1165-39-5
Price: US $0.00-0.00/KG
Min. Order: 1KG
Purity: 99.0%
Supply Ability: 10 tons
Release date: 2024-09-03

Career Henan Chemical Co

Product: Aflatoxin G1 1165-39-5
Price: US $9.80/KG
Min. Order: 1g
Purity: ＞98%
Supply Ability: 20 tons
Release date: 2020-02-10

1165-39-5, AFLATOXIN G1Related Search:

Aflatoxin G1-13C17 Aflatoxin B1-13C17 1,3-DIETHOXYBENZENE 2-METHOXYSTYRENE Phloroglucinol 5,7-DIHYDROXYCOUMARIN 4-Isopropylanisole Methyl tiglate AFLATOXIN G1 2,6-Dimethylphenol 2-METHYL-3-PHENYL-2-PROPEN-1-OL 2'-Methoxycinnamaldehyde 2-Allylphenol 3-Hydroxyphenyl acetate PHENYL METHACRYLATE phenyl propionate 2,3-Dihydrobenzofuran 7-Propoxy-chromen-2-one ,97%

(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

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

(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

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

AFLATOXIN G1(RG) 10mg

1165-39-5

C17H12O7

32827

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