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ChemicalBook > Product Catalogue >Catalyst and Auxiliary >Polyethylene glycol derivatives >Fumonisin B2

Fumonisin B2

Fumonisin B2 Structure
  • ₹23550 - ₹304961.9
  • Product name: Fumonisin B2
  • CAS: 116355-84-1
  • MF: C34H59NO14
  • MW: 705.83
  • EINECS:601-424-4
  • MDL Number:MFCD32197368
  • Synonyms:1,2,3-PROPANETRICARBOXYLIC ACID, 1,1'-[1-(12-AMINO-9,11-DIHYDROXY-2-METHYL-TRIDECYL)-2-(1-METHYLPENTYL)-1,2-ETHANE-DIYL]ESTER;1,2,3-PROPANETRICARBOXYLIC ACID, 1,1'-[1-(12-AMINO-4,11-DIHYDROXY-2-METHYL-TRIDECYL)-2-(1-METHYLPENTYL)-1,2-ETHANE-DIYL]ESTER;FUMONISIN B3;FUMONISIN B2;FUMONISIN B2, FUSARIUM MONILIFORME;FB2;1,2,3-propanetricarboxylicacid,1,1’-(1-(2-amino-9,11-dihydroxy-2-methyltridec ;Fumonisin B2, Ready Made Solution
Price4 Properties Safety Information Description
4 prices
Selected condition：

Brand

  • Sigma-Aldrich(India)

Package

  • 1MG
  • 10MG
  • 1ML
  • ManufacturerSigma-Aldrich(India)
  • Product number344852
  • Product descriptionFumonisin B₂, Fusarium moniliforme - CAS 116355-84-1 - Calbiochem Structural analog of Fumonisin B? that has higher cytotoxicity and specific binding to primary rat hepatocytes than fumonisin B?.
  • Packaging1MG
  • Price₹23550
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product numberF3771
  • Product descriptionFumonisin B2 from Fusarium moniliforme sphingosine N-acyltransferase inhibitor
  • Packaging1MG
  • Price₹47521.75
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product number34142
  • Product descriptionFumonisin B2 solution ~50?μg/mL in acetonitrile: water (50:50), analytical standard
  • Packaging1ML
  • Price₹56365.4
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product numberF3771
  • Product descriptionFumonisin B2 from Fusarium moniliforme sphingosine N-acyltransferase inhibitor
  • Packaging10MG
  • Price₹304961.9
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 344852 Fumonisin B₂, Fusarium moniliforme - CAS 116355-84-1 - Calbiochem Structural analog of Fumonisin B? that has higher cytotoxicity and specific binding to primary rat hepatocytes than fumonisin B?. 1MG ₹23550 2022-06-14 Buy
Sigma-Aldrich(India) F3771 Fumonisin B2 from Fusarium moniliforme sphingosine N-acyltransferase inhibitor 1MG ₹47521.75 2022-06-14 Buy
Sigma-Aldrich(India) 34142 Fumonisin B2 solution ~50?μg/mL in acetonitrile: water (50:50), analytical standard 1ML ₹56365.4 2022-06-14 Buy
Sigma-Aldrich(India) F3771 Fumonisin B2 from Fusarium moniliforme sphingosine N-acyltransferase inhibitor 10MG ₹304961.9 2022-06-14 Buy

Properties

Melting point :<3200(dec)
Boiling point :705.92°C (rough estimate)
Density :1.2044 (rough estimate)
refractive index :1.6630 (estimate)
Flash point :6 °C
storage temp. :-20°C
solubility :DMSO (Slightly), Methanol (Slightly)
pka :3?+-.0.23(Predicted)
form :Off-white solid
color :Off-White to Beige
Stability :Hygroscopic
CAS DataBase Reference :116355-84-1

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H351 Suspected of causing cancer Carcinogenicity Category 2 Warning P201, P202, P281, P308+P313, P405,P501
Precautionary statements:
P201 Obtain special instructions before use.
P202 Do not handle until all safety precautions have been read and understood.
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P308+P313 IF exposed or concerned: Get medical advice/attention.
P405 Store locked up.
P501 Dispose of contents/container to..…

Description

Fumonisin B2 is a mycotoxin originally isolated from F. moniliforme, a prevalent fungus of corn and other grains. Fumonisins cause food poisoning in livestock and humans following the consumption of Fusarium-infested corn. Fumonisin B2, like fumonisin B1 , structurally resembles sphingosine and, at 1 μM, inhibits sphingosine N-acyltransferase (>90%) in hepatocytes. Fumonisins induce apoptosis via altered sphingolipid metabolism, resulting in hepatotoxicity and nephrotoxicity. It is now known that fumonisins are produced by fungi other than F. moniliforme and occur as contaminants in a wide variety of foods.

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