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FUSARENON X

CAS No.
23255-69-8
Chemical Name:
FUSARENON X
Synonyms
Fusarenon;-en-8-one;fusarenonex;-9-en-8-one;7-beta)--bet;Fusarenone X;4-Acetylnivalenol;nivalenolmonoacetate;fusarenon x solution;nivalenol-4-o-acetate
CBNumber:
CB1503492
Molecular Formula:
C17H22O8
Molecular Weight:
354.35
MDL Number:
MFCD00078778
MOL File:
23255-69-8.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-27 23:40:12

FUSARENON X Properties

Melting point 91-92℃
Boiling point 407.59°C (rough estimate)
Density 1.2646 (rough estimate)
refractive index 1.4430 (estimate)
Flash point 2 °C
storage temp. −20°C
solubility Dichloromethane: Soluble
pka 11.70±0.70(Predicted)
Henry's Law Constant 2.1×1011 mol/(m3Pa) at 25℃, HSDB (2015)
CAS DataBase Reference 23255-69-8
FDA UNII 0CV8D1DR96

SAFETY

Risk and Safety Statements

Symbol(GHS)  Skull and Crossbones (GHS06)
GHS06
Signal word  Danger
Hazard statements  H300-H315-H319-H335
Precautionary statements  P301+P310+P330-P302+P352-P305+P351+P338
Hazard Codes  F,Xn,T+
Risk Statements  11-20/21/22-36-36/37/38-28
Safety Statements  26-36/37-45-36/37/39-22-16
RIDADR  3172
WGK Germany  3
RTECS  YD0160000
HazardClass  6.1(a)
PackingGroup  I
HS Code  2932990090
Hazardous Substances Data 23255-69-8(Hazardous Substances Data)
NFPA 704
0
2 0

FUSARENON X price More Price(19)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 34130 Fusarenon X solution 100μg/mL in acetonitrile, analytical standard 23255-69-8 2ml $568 2026-04-30 Buy
Sigma-Aldrich 33438 Fusarenon X analytical standard 23255-69-8 5mg $1370 2026-04-30 Buy
Cayman Chemical 11432 Fusarenon X ≥99% 23255-69-8 100μg $49 2026-04-30 Buy
Cayman Chemical 11432 Fusarenon X ≥99% 23255-69-8 250μg $107 2026-04-30 Buy
Cayman Chemical 11432 Fusarenon X ≥99% 23255-69-8 500μg $202 2026-04-30 Buy
Product number Packaging Price Buy
34130 2ml $568 Buy
33438 5mg $1370 Buy
11432 100μg $49 Buy
11432 250μg $107 Buy
11432 500μg $202 Buy

FUSARENON X Chemical Properties,Uses,Production

Description

Fusarenon X is a type B trichothecene mycotoxin typically derived from Fusarium species. It is primarily found in contaminated cereals. Fusarenon X inhibits protein synthesis, which leads to disruption of DNA synthesis. As this occurs in actively proliferating cells, fusarenon X causes immunosuppression, intestinal malabsorption, developmental toxicity, and genotoxicity. Fusarenon X can be metabolized to fusarenon X-glucoside by infected plants.

Uses

A mycotoxin produced by Fusarium, having immunosuppressive and carcinogenic properties.

Safety Profile

Poison by ingestion, subcutaneous, intravenous, and intraperitoneal routes. An experimental teratogen. Experimental reproductive effects. Questionable carcinogen with experimental tumorigenic data. Human mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes.

References

[1] SAWINEE AUPANUN. An overview of the toxicology and toxicokinetics of fusarenon-X, a type B trichothecene mycotoxin.[J]. Journal of Veterinary Medical Science, 2017, 79 1: 6-13. DOI: 10.1292/jvms.16-0008
[2] FRANZ BERTHILLER. Masked mycotoxins: A review[J]. Molecular Nutrition & Food Research, 2012, 57 1: 165-186. DOI: 10.1002/mnfr.201100764

FUSARENON X Preparation Products And Raw materials

Raw materials

Preparation Products

4-acetyloxy-12,13-epoxy-3,7,15-trihydroxy-(3-alpha,4-beta,7-beta)-trichothec-9 7-beta)--bet -9-en-8-one -en-8-one Fusarenone X fusarenonex nivalenol-4-o-acetate 12,13-epoxy-3alpha,4beta,7beta,15-tetrahydroxy-trichothec-9-en-8-on4-aceta 12,13-epoxy-3-alpha,4-beta,7-beta,15-tetrahydroxytrichothec-9-en-8-one4-acet 3,7,15-trihydroxy-4-acetoxy-8-oxo-12,13-epoxy-delta(sup9)-trichothecene 3,7,15-trihydroxyscirp-4-acetoxy-9-en-8-one 4-acetyloxy-12,13-epoxy-3,7,15-trihydroxy-(3-alpha,4-beta,7-beta)-trichothec nivalenolmonoacetate Trichothec-9-en-8-one, 12,13-epoxy-3alpha,4beta,7beta,15-tetrahydroxy-, 4-acetate Trichothec-9-en-8-one, 4-(acetyloxy)-12,13-epoxy-3,7,15-trihydroxy-, (3alpha,4beta,7beta)- trichothec-9-en-8-one,4-(acetyloxy)-12,13-epoxy-3,7,15-trihydroxy-,(3-alpha,4 trichothec-9-en-8-one,4-(acetyloxy)-12,13-epoxy-3,7,15-trihydroxy-,(3alpha,4b 3α,7α,15-trihydroxy-4β-acetoxy-12,13-epoxytrichothec-9-en-8-one fusarenon x solution FUSARENON X SOLUTION (100&MU FusX, 3α,7α,15-Trihydroxy-4β-acetoxy-12,13-epoxytrichothec-9-en-8-one 3α,7α,15-Trihydroxy-4β-acetoxy-12,13-epoxytrichotheca-9-ene-8-one 4-Acetylnivalenol 4β-(Acetyloxy)-12,13-epoxy-3α,7α,15-trihydroxytrichothec-9-en-8-one Fusarenon X solution,3α,7α,15-Trihydroxy-4β-acetoxy-12,13-epoxytrichothec-9-en-8-one, FusX 4beta-Acetoxy-3alpha,7alpha,15-trihydroxy-12,13-epoxytrichothec-9-en-8-one Nivalenol monoacetate, 12,13-epoxy-3 alpha,4 beta,7 beta,15-tetrahydroxytrichothec-9-en-8-one 4-acetate Fusarenon X from Fusarium nivale XGCUCFKWVIWWNW-GXKXROSLSA-N Trichothec-9-en-8-one, 4-(acetyloxy)-12,13-epoxy-3,7,15-trihydroxy-, (3α,4β,7α)- Trichothec-9-en-8-one Fusarenon 23255-69-8 C17H22O8 Chiral Reagents Intermediates & Fine Chemicals Mutagenesis Research Chemicals Pharmaceuticals mycotoxin