2,4-DB

2,4-DB[1][2]
2,4-DB
Names
Preferred IUPAC name
4-(2,4-Dichlorophenoxy)butanoic acid
Other names
  • (2,4-Dichlorophenoxy)butyric acid
  • Butirex
  • Butyrac
  • Embutone
  • Embutox
  • Venceweed
Identifiers
CAS Number
  • 94-82-6 checkY
3D model (JSmol)
  • Interactive image
Beilstein Reference
1976809
ChEBI
  • CHEBI:73173
ChemSpider
  • 1444 checkY
ECHA InfoCard 100.002.152 Edit this at Wikidata
KEGG
  • C14404 checkY
PubChem CID
  • 1489
RTECS number
  • ES9100000
UNII
  • SL314DW868 checkY
UN number 3082
CompTox Dashboard (EPA)
  • DTXSID7024035 Edit this at Wikidata
InChI
  • InChI=1S/C10H10Cl2O3/c11-7-3-4-9(8(12)6-7)15-5-1-2-10(13)14/h3-4,6H,1-2,5H2,(H,13,14) checkY
    Key: YIVXMZJTEQBPQO-UHFFFAOYSA-N checkY
  • InChI=1/C10H10Cl2O3/c11-7-3-4-9(8(12)6-7)15-5-1-2-10(13)14/h3-4,6H,1-2,5H2,(H,13,14)
    Key: YIVXMZJTEQBPQO-UHFFFAOYAK
  • Clc1cc(Cl)ccc1OCCCC(=O)O
Properties
Chemical formula
C10H10Cl2O3
Molar mass 249.09 g/mol
Appearance Colorless to white crystal
Melting point 117 to 119 °C (243 to 246 °F; 390 to 392 K)
Solubility in water
46 mg/L
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Persistent hazard to marine life.
GHS labelling:
Pictograms
GHS07: Exclamation mark GHS05: Corrosive
Warning
H302, H411[2]
P264, P270, P273, P301+P312, P330, P391, P501[2]
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chlorideFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
0
0
0
Lethal dose or concentration (LD, LC):
1.97 mg/L - 96.0 h (Rainbow Trout)[2]
Safety data sheet (SDS) Sigma-Aldrich Site
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Chemical compound

2,4-DB or 4-(2,4-dichlorophenoxy)butyric acid is a selective systemic phenoxy herbicide used to control many annual and perennial broad-leaf weeds in alfalfa, peanuts, soybeans, and other crops. Its active metabolite, 2,4-D, inhibits growth at the tips of stems and roots. It is classified in toxicity class III. It shows some evidence of toxicity to dogs and cats, such as changes in body weight and reduced numbers of offspring, when fed 25-80 milligrams per kilogram of body weight for prolonged periods. Tests of carcinogenicity in this range yielded differing results. It is moderately toxic to fish.[1]

References

  1. ^ a b "Extension Toxicology Network: Pesticide Information Profiles". Archived from the original on 10 May 2008. Retrieved 15 June 2008.
  2. ^ a b c d "2,4-DB SDS". Sigma-Aldrich. Sigma Aldrich. Retrieved 14 May 2018.
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