Meptyldinocap
| Code | Size | Price |
|---|
| CDX-M0311-M025 | 25 mg | £139.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
+4°C
Documents
Further Information
Alternate Names/Synonyms:
2,4-DNOPC; (RS)-2-(1-Methylheptyl)-4,6-dinitrophenyl crotonate; 2-(1-Methylheptyl)-4,6-dinitrophenyl (2E)-2-butenoate
Appearance:
Yellowish to brown liquid.
CAS:
131-72-6
Class:
9
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07,GHS08,GHS09
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H302, H332, H315, H317, H360D, H373, H410
InChi:
InChI=1S/C18H24N2O6/c1-4-6-7-8-10-13(3)15-11-14(19(22)23)12-16(20(24)25)18(15)26-17(21)9-5-2/h5,9,11-13H,4,6-8,10H2,1-3H3/b9-5+
InChiKey:
NIOPZPCMRQGZCE-WEVVVXLNSA-N
Long Description:
Chemical. CAS: 131-72-6. Formula: C18H24N2O6. MW: 364.4. Synthetic. Powdery mildew (Erysiphe necator) dinitrophenol fungicide. Stops cellular energy production. Interferes with fungal respiration by acting as an uncoupler of oxidative phosphorylation. Compound can be used as analytical reference material.
MDL:
MFCD00054268
Molecular Formula:
C18H24N2O6
Molecular Weight:
364.4
Package Type:
Vial
PG:
III
Precautions:
P201, P273, P280, P308, P313, P501
Product Description:
Powdery mildew (Erysiphe necator) dinitrophenol fungicide. Stops cellular energy production. Interferes with fungal respiration by acting as an uncoupler of oxidative phosphorylation. Compound can be used as analytical reference material.
Purity:
>98% (HPLC)
Signal Word:
Danger
SMILES:
O=C(/C=C/C)OC1=C(C(CCCCCC)C)C=C([N+]([O-])=O)C=C1[N+]([O-])=O
Solubility Chemicals:
Soluble in acetone or ethyl acetate. Insoluble in water.
Source / Host:
Synthetic.
Transportation:
Excepted Quantity
UN Nummer:
UN 3082
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.
References
(1) G. Gilardi, et al.; Commun. Agric. Appl. Biol. Sci. 73, 21 (2008) | (2) S.E. Legler, et al.; J. Plant Pathol. 94, 66 (2012)