523844
3,6-Dichloro-2-methoxybenzoic acid
97%
Synonym(s):
Dicamba, 3,6-Dichloro-2-methoxybenzoic acid, 3,6-Dichloro-o-anisic acid
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About This Item
Linear Formula:
Cl2C6H2(OCH3)CO2H
CAS Number:
Molecular Weight:
221.04
EC Number:
217-635-6
UNSPSC Code:
12352200
MDL number:
Beilstein/REAXYS Number:
2453039
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InChI
1S/C8H6Cl2O3/c1-13-7-5(10)3-2-4(9)6(7)8(11)12/h2-3H,1H3,(H,11,12)
InChI key
IWEDIXLBFLAXBO-UHFFFAOYSA-N
SMILES string
COc1c(Cl)ccc(Cl)c1C(O)=O
assay
97%
mp
112-116 °C (lit.)
comparable product
Product No.
Description
Pricing
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Franciso P Peixoto et al.
Journal of plant physiology, 165(11), 1125-1133 (2008-04-26)
The effects of the herbicides 1,1'-dimethyl-4,4'-bipyridylium dichloride (paraquat), 3,6-dichloro-2-metoxybenzoic acid (dicamba) and 2,4-dichlorophenoxyacetic acid (2,4-D) on cell growth of non-green potato tuber calli are described. We attempted to relate the effects with toxicity, in particular the enzymes committed to the
Süleyman Cenkci et al.
Ecotoxicology and environmental safety, 73(7), 1558-1564 (2010-08-28)
The present study was undertaken to evaluate genotoxic potential of two auxinic herbicides [2,4-dicholorophenoxy acetic acid (2,4-D) and 3,6-dichloro-2-methoxybenzoic acid (Dicamba)] in the roots of common bean (Phaseolus vulgaris L.) seedlings. Two-day-old etiolated seedlings were treated with 10 ppm methyl
N V González et al.
Toxicology letters, 207(3), 204-212 (2011-10-04)
The purpose of this study was to further investigate the cytotoxic and genotoxic effects of dicamba and Banvel(®) employing the cytokinesis-block micronucleus cytome (CBMN-cyt) assay estimated by the analysis of the nuclear division index (NDI), the frequency of micronucleus (MN)
Eun-Ho Shin et al.
Biomedical chromatography : BMC, 25(1-2), 124-135 (2010-09-16)
2,4-D, dicamba and 4-CPA with auxin-like activity have been intensively used in agriculture, for the control of unwanted broadleaf weeds. An analytical method involving HPLC coupled with UVD was developed for the simultaneous analysis of these three analytes in Chinese
J Franklin Egan et al.
Environmental toxicology and chemistry, 31(5), 1023-1031 (2012-03-01)
Recent advances in biotechnology have produced cultivars of corn, soybean, and cotton resistant to the synthetic-auxin herbicide dicamba. This technology will allow dicamba herbicides to be applied in new crops, at new periods in the growing season, and over greatly
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