Chemodex

Flumiclorac

Product Code:
 
CDX-F0085
Product Group:
 
Other Biochemicals
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
-20°C
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Chemical Structure
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Chemical Structure

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CodeSizePrice
CDX-F0085-M05050 mg£108.00
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CDX-F0085-M250250 mg£437.00
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CDX-F0085-G0011 g£1,157.00
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This product comes from: Switzerland.
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Further Information

Alternate Names/Synonyms:
2-[2-chloro-4-fluoro-5-(1,3,4,5,6,7-hexahydro-1,3-dioxo-2H-isoindol-2-yl)phenoxy]acetic acid
Appearance:
White powder.
CAS:
87547-04-4
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H302, H315, H319, H335
InChi:
InChI=1S/C16H13ClFNO5/c17-10-5-11(18)12(6-13(10)24-7-14(20)21)19-15(22)8-3-1-2-4-9(8)16(19)23/h5-6H,1-4,7H2,(H,20,21)
InChiKey:
GQQIAHNFBAFBCS-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 87547-04-4. Formula: C16H13ClFNO5. MW: 353.73. Synthetic Herbicide. Mode of action is similar to herbicides that inhibit the protoporphyrinogen oxidase (Protox) enzyme in susceptible plant species that leads to an uncontrolled nonenzymatic oxidation of protoporphyrinogen IX (Protogen) to protoporphyrin IX (Proto) and successive necrosis.
MDL:
MFCD18449905
Molecular Formula:
C16H13ClFNO5
Molecular Weight:
353.73
Package Type:
Vial
Precautions:
P261, P305, P351, P338
Product Description:
Herbicide. Mode of action is similar to herbicides that inhibit the protoporphyrinogen oxidase (Protox) enzyme in susceptible plant species that leads to an uncontrolled nonenzymatic oxidation of protoporphyrinogen IX (Protogen) to protoporphyrin IX (Proto) and successive necrosis.
Purity:
>98% (HPLC)
Signal word:
Warning
SMILES:
OC(=O)COC1=C(Cl)C=C(F)C(=C1)N1C(=O)C2=C(CCCC2)C1=O
Solubility Chemicals:
Sligthly soluble in water.
Source / Host:
Synthetic
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

References

(1) N.B. Birchfield & J.E. Casida; Pest. Biochem. Physiol. 57, 36 (1997) | (2) J.C. Fausey, et al.; Weed Sci. 48, 405 (2000) | (3) K.A. Nelson, et al.; Weed Technol. 16, 353 (2002)