Pyributicarb
| Code | Size | Price |
|---|
| CDX-P0129-M100 | 100 mg | £151.00 |
Quantity:
| CDX-P0129-M250 | 250 mg | £291.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
+20°C
Documents
Further Information
Alternate Names/Synonyms:
O-3-tert-Butylphenyl 6-methoxy-2-pyridyl(methyl)thiocarbamate ; O-[3-(1,1-Dimethylethyl)phenyl] N-(6-methoxy-2-pyridinyl)-N-methylcarbamothioate
Appearance:
White crystalline powder.
CAS:
88678-67-5
Class:
9
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS09
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H410
InChi:
InChI=1S/C18H22N2O2S/c1-18(2,3)13-8-6-9-14(12-13)22-17(23)20(4)15-10-7-11-16(19-15)21-5/h6-12H,1-5H3
InChiKey:
VTRWMTJQBQJKQH-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 88678-67-5. Formula: C18H22N2O2S. MW: 330.4. Synthetic. Thiocarbamate herbicide with fungicidal activity. Inhibits 4-hydroxyphenyl-pyruvatedioxygenase (4-HPPD) in plants that causes bleaching. And targets squalene-epoxidase in sterol biosynthesis in fungus. Compound can be used as analytical reference material.
MDL:
MFCD00468117
Molecular Formula:
C18H22N2O2S
Molecular Weight:
330.4
Package Type:
Vial
Precautions:
P273, P501
Product Description:
Thiocarbamate herbicide with fungicidal activity. Inhibits 4-hydroxyphenyl-pyruvatedioxygenase (4-HPPD) in plants that causes bleaching. And targets squalene-epoxidase in sterol biosynthesis in fungus. Compound can be used as analytical reference material.
Purity:
>98% (HPLC)
Signal word:
Warning
SMILES:
S=C(OC1=CC=CC(C(C)(C)C)=C1)N(C2=NC(OC)=CC=C2)C
Solubility Chemicals:
Soluble in acetone, ethyl acetate, methanol or ethanol. Insoluble in water.
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UN Nummer:
UN 3077
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at +4°C.
References
(1) K. Tsuzuki; J. Pest. Inform. 57, 30 (1990) | (2) K. Tsuzuki; J. Weed Sci. Techn. 39, 19 (1994) | (3) A. Belter; Biol. Chem. 392, 1053 (2011)
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