Skip to Content
Merck
CN

D5417

Dicamba

suitable for plant cell culture, BioReagent

Synonym(s):

3,6-Dichloro-2-methoxybenzoic acid, 3,6-Dichloro-o-anisic acid

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
Cl2C6H2(OCH3)CO2H
CAS Number:
1918-00-9
Molecular Weight:
221.04
UNSPSC Code:
10171502
NACRES:
NA.72
PubChem Substance ID:
24893833
EC Number:
217-635-6
Beilstein/REAXYS Number:
2453039
MDL number:
MFCD00055283

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

IWEDIXLBFLAXBO-UHFFFAOYSA-N

InChI

1S/C8H6Cl2O3/c1-13-7-5(10)3-2-4(9)6(7)8(11)12/h2-3H,1H3,(H,11,12)

SMILES string

COc1c(Cl)ccc(Cl)c1C(O)=O

product line

BioReagent

form

powder

technique(s)

cell culture | plant: suitable

mp

112-116 °C (lit.)

application(s)

agriculture

storage temp.

2-8°C

Quality Level

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Dicamba (3,6-dichloro-2-methoxybenzoic acid) is an organochlorine compound, with plant growth auxin characteristics.

Application

Dicamba has been used:
  • as an auxin to maintain wheat embryos post pollination
  • as a Murashige and Skoog (MS) medium supplement to culture embryos
  • as an auxin in induction medium to induce somatic embryogenesis in barely tissue culture

Biochem/physiol Actions

Dicamba is a broad leaf growth regulator that mimics plant growth auxins. Dicamba is used as a herbicide and is effective against glyphosate-resistant (GR) giant ragweed.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Preparation Note

Preparation and Use

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

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

Regulatory Information

农药列管产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCN5380
BCCL3230
013M3906
BCBL0437V
BCBM8855

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Generation of amphidiploids from hybrids of wheat and related species from the genera Aegilops, Secale, Thinopyrum, and Triticum as a source of genetic variation for wheat improvement
Nemeth C, et al.
Genome / National Research Council Canada = Genome / Conseil National de Recherches Canada, 58(2), 71-79 (2015)
B S Clegg et al.
Journal of agricultural and food chemistry, 49(5), 2168-2174 (2001-05-23)
A competitive indirect enzyme-linked immunosorbent assay (CI-ELISA) was developed to quantitate the herbicide dicamba (3,6-dichloro-2-methoxybenzoic acid) in water. The CI-ELISA has a detection limit of 2.3 microg L(-1) and a linear working range of 10--10000 microg L(-1) with an IC(50)
Interaction of 2, 4-D or dicamba with glufosinate for control of glyphosate-resistant giant ragweed (Ambrosia trifida L.) in glufosinate-resistant maize (Zea mays L.)
Ganie ZA and Jhala AJ
Frontiers in Plant Science, 8, 1207-1207 (2017)
Adsorption of Dicamba herbicide onto a carbon replica obtained from a layered double hydroxide
Pinto MCE
Dalton Transactions, 47(9), 3119-3127 (2018)
Dicamba
Cox C
JOURNAL OF PESTICIDE REFORM, 4 (1994)
View All Related Papers

Related Content

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service