Dinoterb: Difference between revisions

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	{{Distinguish\|~~Dinoseb~~}}		{{Distinguish\|dinoseb}}

	{{one source\|date=October 2014}}
	{{Chembox		{{Chembox
	\| ImageFile = Dinoterb.svg		\| ImageFile = Dinoterb structure.svg
	\| ImageSize = 180px		\| ImageSize = 180px
	\| IUPACName = 2-(2-~~Methyl-2-propanyl)~~-4,6-dinitrophenol		\| IUPACName = 2-''tert''-Butyl-4,6-dinitrophenol
	\| OtherNames =		\| OtherNames =
	\|Section1={{Chembox Identifiers		\|Section1={{Chembox Identifiers
	\| CASNo = 1420-07-1		\| CASNo = 1420-07-1
			\| CASNo_Ref = {{cascite\|correct\|CAS}}
			\| UNII_Ref = {{fdacite\|correct\|FDA}}
			\| UNII = 2O5H456CFI
	\| PubChem = 14994		\| PubChem = 14994
	\| ChemSpiderID = 14274		\| ChemSpiderID = 14274
	\| SMILES = (=O)c1cc(cc(c1O)C(C)(C)C)()=O		\| SMILES = (=O)c1cc(cc(c1O)C(C)(C)C)()=O
	\| InChI = 1/C10H12N2O5/c1-10(2,3)7-4-6(11(14)15)5-8(9(7)13)12(16)17/h4-5,13H,1-3H3
	\| InChIKey = IIPZYDQGBIWLBU-UHFFFAOYAT
	\| StdInChI = 1S/C10H12N2O5/c1-10(2,3)7-4-6(11(14)15)5-8(9(7)13)12(16)17/h4-5,13H,1-3H3		\| StdInChI = 1S/C10H12N2O5/c1-10(2,3)7-4-6(11(14)15)5-8(9(7)13)12(16)17/h4-5,13H,1-3H3
	\| StdInChIKey = IIPZYDQGBIWLBU-UHFFFAOYSA-N		\| StdInChIKey = IIPZYDQGBIWLBU-UHFFFAOYSA-N
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	\| Appearance =		\| Appearance =
	\| Density = 1.35 g/cm<sup>3</sup>		\| Density = 1.35 g/cm<sup>3</sup>
	\| ~~MeltingPt~~ = 125.5-126.5 °C		\| MeltingPtC = 125.5-126.5
			\| MeltingPt_ref = <ref name = GESTIS>{{GESTIS\|ZVG=510198}}</ref>
	\| BoilingPt =		\| BoilingPt =
	\| Solubility =		\| Solubility = 0.45 mg/L (20 °C)<ref name = GESTIS/>
	}}		}}
	\|Section3={{Chembox Hazards		\|Section3={{Chembox Hazards
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	\| FlashPt =		\| FlashPt =
	\| AutoignitionPt =		\| AutoignitionPt =
			\| LD50 = 26 mg/kg (rat, oral)
	}}		}}
	}}		}}

			'''Dinoterb''' is a ] previously used as a contact ]. It is an ], affecting respiration in ] and photosynthesis in ]. It is banned for use in the European Union and use was suspended in the United States in 1986.<ref>{{cite web \|title=Dinoterb \|url=https://pubchem.ncbi.nlm.nih.gov/compound/Dinoterb \|website=PubChem \|publisher=National Library of Medicine \|access-date=14 December 2023 \|language=en}}</ref>
	'''Dinoterb''' is a ] used in ].<ref> at www.alanwood.net.</ref>

	==References==		==References==
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	]		]
	]		]
	]		]
			]

	{{Organic-compound-stub}}		{{Organic-compound-stub}}

Latest revision as of 19:25, 30 January 2024

Not to be confused with dinoseb.

Dinoterb
Names

IUPAC name 2-tert-Butyl-4,6-dinitrophenol
Identifiers
CAS Number	1420-07-1
3D model (JSmol)	Interactive image
ChemSpider	14274
ECHA InfoCard	100.014.376
PubChem CID	14994
UNII	2O5H456CFI
CompTox Dashboard (EPA)	DTXSID7041883
InChI InChI=1S/C10H12N2O5/c1-10(2,3)7-4-6(11(14)15)5-8(9(7)13)12(16)17/h4-5,13H,1-3H3Key: IIPZYDQGBIWLBU-UHFFFAOYSA-N
SMILES (=O)c1cc(cc(c1O)C(C)(C)C)()=O
Properties
Chemical formula	C₁₀H₁₂N₂O₅
Molar mass	240.215 g·mol
Density	1.35 g/cm
Melting point	125.5–126.5 °C (257.9–259.7 °F; 398.6–399.6 K)
Solubility in water	0.45 mg/L (20 °C)
Hazards
Lethal dose or concentration (LD, LC):
LD₅₀ (median dose)	26 mg/kg (rat, oral)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references

Chemical compound

Dinoterb is a chemical compound previously used as a contact herbicide. It is an uncoupler, affecting respiration in mitochondria and photosynthesis in chloroplasts. It is banned for use in the European Union and use was suspended in the United States in 1986.

References

^ Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health
"Dinoterb". PubChem. National Library of Medicine. Retrieved 14 December 2023.

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