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Dicamba

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Identification
Molecular formula
C8H6Cl2O3
CAS number
1918-00-9
IUPAC name
3,6-dichloro-2-methoxy-benzoic acid
State
State

Dicamba is solid at room temperature.

Melting point (Celsius)
114.50
Melting point (Kelvin)
387.65
Boiling point (Celsius)
305.42
Boiling point (Kelvin)
578.57
General information
Molecular weight
221.05g/mol
Molar mass
221.0460g/mol
Density
1.5000g/cm3
Appearence

Dicamba is typically a white crystalline solid.

Comment on solubility

Solubility of 3,6-Dichloro-2-methoxy-benzoic Acid

3,6-Dichloro-2-methoxy-benzoic acid (C8H6Cl2O3) exhibits interesting solubility properties that are influenced by its structural characteristics. Understanding the solubility of this compound can provide insights into its behavior in various solvents. Here are some key points about its solubility:

  • Polar Solvents: Due to the presence of the carboxylic acid group (-COOH), this compound tends to be soluble in polar solvents such as water and alcohols.
  • Non-Polar Solvents: Its dichlorobenzene structure suggests limited solubility in non-polar solvents, which may be attributed to steric hindrance and molecular interactions.
  • pH Dependency: The solubility in water can be affected by the pH of the solution. In acidic conditions, the compound remains predominantly in its uncharged form, while in basic conditions, it can ionize, increasing its solubility.
  • Thermodynamic Considerations: The dissolution process is likely endothermic, meaning it can absorb heat from the surroundings while dissolving.

As a result, the solubility of 3,6-dichloro-2-methoxy-benzoic acid is characterized by a complex interplay of factors including polarity, functional groups, and environmental conditions.

Interesting facts

Interesting Facts about 3,6-Dichloro-2-methoxy-benzoic Acid

3,6-dichloro-2-methoxy-benzoic acid is a fascinating compound that belongs to a class of organic compounds known as substituted benzoic acids. It is recognized for its unique structure and various applications in both the chemical industry and biological systems.

Key Characteristics

  • Functional Groups: This compound features both carboxylic acid and methoxy groups, which significantly influence its chemical behavior and reactivity.
  • Chlorine Substituents: The presence of chlorine atoms at the 3 and 6 positions provides enhanced biological activity, making this compound a subject of interest for pharmaceutical research.
  • Synthesis: It can be synthesized through various organic reactions, including chlorination and methoxylation, making it an interesting target for students learning about organic synthesis.

Applications

3,6-dichloro-2-methoxy-benzoic acid has several noteworthy applications:

  • Herbicide Development: This compound is explored for its potential use as an herbicide, showcasing its ability to inhibit plant growth effectively.
  • Pharmaceutical Research: Researchers are investigating its derivatives for antimicrobial and antifungal properties, demonstrating the compound’s potential in drug formulation.

As with many chlorine-containing compounds, it is essential to handle 3,6-dichloro-2-methoxy-benzoic acid with care due to its environmental impact and biological activity. In summary, this compound not only provides chemical insight but also serves as a reminder of the intricate relationships between structure, reactivity, and application in the field of chemistry.

Quote to Consider

As the renowned chemist Robert H. Grubbs once said, "Science is all about the connections between seemingly unrelated phenomena." This quote is an apt reminder of how studying compounds like 3,6-dichloro-2-methoxy-benzoic acid can lead to unexpected discoveries in both science and industry.

Synonyms
dicamba
1918-00-9
3,6-Dichloro-2-methoxybenzoic acid
Benzoic acid, 3,6-dichloro-2-methoxy-
Banvel
Mdba
3,6-Dichloro-o-anisic acid
Mediben
Dianat
Banlen
Brush buster
Banvel herbicide
o-Anisic acid, 3,6-dichloro-
Banvel CST
Banvel SGF
Compound B dicamba
Velsicol compound R
Banvel II herbicide
Banvel 70WP
Aviator
Banvel 480
Caswell No. 295
Celebrity B
Compound B [Velsicol]
Mais Banvel WG
Velsicol 58-CS-11
Dicamba [ISO]
Dicamba [ANSI:BSI:ISO]
62610-39-3
2,5-Dichloro-6-methoxybenzoic acid
2-Methoxy-3,6-dichlorobenzoic acid
3,6-dichloro-2-methoxy-benzoic acid
CCRIS 1471
HSDB 311
SJG3M6RY6H
EINECS 217-635-6
MFCD00055283
Dianate
Banex (Salt/Mix)
EPA Pesticide Chemical Code 029801
BRN 2453039
DTXSID4024018
CHEBI:81856
AI3-27556
Banvel D (Salt/Mix)
DICAMBA [HSDB]
DICAMBA [MI]
3,6-Dichloor-2-methoxy-benzoeizuur
3,6-Dichlor-3-methoxy-benzoesaeure
Banvel 4S (Salt/Mix)
Fallow master (Salt/Mix)
Banvel 200 (Salt/Mix)
Kyselina 3,6-dichlor-2-methoxybenzoova
Acido (3,6-dicloro-2-metossi)-benzoico
DTXCID904018
IWEDIXLBFLAXBO-UHFFFAOYSA-
Dicamba 10 microg/mL in Acetonitrile
Dicamba 100 microg/mL in Acetonitrile
Compound B (Velsicol)
Dianat [Russian]
Dicamba (ANSI:BSI:ISO)
CAS-1918-00-9
Velsicol 58CS11
UNII-SJG3M6RY6H
Fallowmaster
Dicambe
Dicambra
Metambane
Trooper
3,6-Dichloor-2-methoxy-benzoeizuur [Dutch]
3,6-Dichlor-3-methoxy-benzoesaeure [German]
Banvel 4ws
Kyselina 3,6-dichlor-2-methoxybenzoova [Czech]
D3M
Acido (3,6-dicloro-2-metossi)-benzoico [Italian]
Dicamba D3 solution
Velsicol compound "R
Velsicol Compound''R
Spectrum_001827
SpecPlus_000428
3,6Dichlorooanisic acid
Spectrum2_001882
Spectrum3_000824
Spectrum4_000664
Spectrum5_001960
Velsicol Compound ''R''
BENZOIC ACID,3,6-DICHLORO-2-METHOXY-
oAnisic acid, 3,6dichloro
Oprea1_626816
SCHEMBL18336
BSPBio_002347
KBioGR_001067
KBioSS_002332
SPECTRUM330032
Dicamba benzoic acid herbicide
DivK1c_006524
3,6Dichloor2methoxybenzoeizuur
3,6Dichlor3methoxybenzoesaeure
SPBio_001784
CHEMBL476936
2,5Dichloro6methoxybenzoic acid
2Methoxy3,6dichlorobenzoic acid
3,6Dichloro2methoxybenzoic acid
3,6 Dichloromethoxybenzoic Acid
KBio1_001468
KBio2_002329
KBio2_004897
KBio2_007465
KBio3_001847
Acido (3,6dicloro2metossi)benzoico
DICAMBA, [RING-14C(U)]
Kyselina 3,6dichlor2methoxybenzoova
MSK22526
Tox21_201356
Tox21_300661
CCG-39335
STL455891
2-methoxy-3,6-dichloro-benzoic acid
3, 6-DICHLORO-O-ANISIC ACID
AKOS000273802
KS-5270
USEPA/OPP Pesticide Code: 029801
NCGC00094526-01
NCGC00094526-02
NCGC00094526-03
NCGC00094526-04
NCGC00094526-05
NCGC00094526-06
NCGC00094526-07
NCGC00254569-01
NCGC00258908-01
FD159958
SY107360
DB-022124
DB-356686
Dicamba, PESTANAL(R), analytical standard
HY-121267
CS-0081338
D4800
NS00000253
Dicamba (3,6-dichloro-2-methoxybenzoic acid)
C18597
Dicamba, plant cell culture tested, BioReagent
H10363
EN300-8153644
Q424684
Dicamba, certified reference material, TraceCERT(R)
2-(2-aminoethoxy)ethanol salt of 3,6-dichloro-o-anisic acid.
217-635-6
89300-29-8
Trade names: Banfel, Banvel, Banvel CST, Banvel D, Banvel XG, Dianat, Dicazin, Fallowmaster, Mediben, Metambane, Tracker, and Trooper