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ChemicalBook >> CAS DataBase List >>OCHRATOXIN A

OCHRATOXIN A suppliers

OCHRATOXIN A

CAS:
303-47-9
MF:
C20H18ClNO6
MW:
403.81

Company Type

Properties

Melting point:
169°C
alpha 
D -118° (c = 1.1 in CHCl3)
Boiling point:
632.4±55.0 °C(Predicted)
Density 
1.2459 (rough estimate)
refractive index 
1.6000 (estimate)
Flash point:
2 °C
storage temp. 
2-8°C
solubility 
ethanol: soluble
pka
3.29±0.10(Predicted)
form 
powder
color 
White to off-white
Merck 
13,6772
BRN 
8169012

Safety Information

Symbol(GHS) 
GHS hazard pictogramsGHS hazard pictograms
GHS06,GHS08
Signal word 
Danger
Hazard statements 
H300+H310+H330-H350-H360
Precautionary statements 
P202-P260-P264-P280-P302+P352+P310-P304+P340+P310
Hazard Codes 
T+,T,Xn,F
Risk Statements 
45-46-61-26/27/28-36-20/21/22-11-40-28-39/23/24/25-23/24/25-65-48/23/24/25-36/38
Safety Statements 
53-22-36/37/39-45-36-26-16-36/37-28-62
RIDADR 
UN 3462 6.1/PG 2
WGK Germany 
3
RTECS 
AY4375000
10
HazardClass 
6.1(a)
PackingGroup 
I
HS Code 
29322985
Toxicity
LD50 orally in rats: 20-22 mg/kg (Purchase, Theron)

Use

Ochratoxin A is a chlorinated benzopyran coupled to phenylalanine, produced by several Aspergillus and Penicillium sp. associated with food spoilage. Ochratoxins are widely distributed in the environment and are known to be nephrotoxic, teratogenic and possibly carcinogenic. Ochratoxin A may act by inducing DNA strand breaks, sister chromatid exchanges, DNA adduct formation, or reactive oxygen but the mechanism of action as a toxin is not yet resolved. At the molecular level, ochratoxin A specifically inhibits NK cell activity, increases growth of transplantable tumor cells in mice, increases apoptosis, activates c-Jun N terminal kinase in human kidney epithelial cells, and blocks metaphase/anaphase transition. It also inhibits plasminogen activator inhibitor-2 production by human blood mononuclear cells.

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