Misplaced Pages

O-Anisidine: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editContent deleted Content addedVisualWikitext
Revision as of 07:33, 9 June 2011 editPashihiko (talk | contribs)Extended confirmed users3,559 editsNo edit summary← Previous edit Latest revision as of 20:15, 1 November 2024 edit undoJWBE (talk | contribs)Extended confirmed users10,126 edits +Category:Anisidines; ±Category:Anilines→Category:2-Aminophenyl compounds using HotCat 
(44 intermediate revisions by 21 users not shown)
Line 1: Line 1:
{{DISPLAYTITLE:''o''-Anisidine}} {{DISPLAYTITLE:''o''-Anisidine}}
{{chembox {{Chembox
| Verifiedfields = changed
⚫ | verifiedrevid = 396509651
| Watchedfields = changed
⚫ | verifiedrevid = 433349433
| Name = ''o''-Anisidine | Name = ''o''-Anisidine
| ImageFile = 2-Anisidine.png | ImageFileL1 = 2-Anisidine.png
| ImageSize = 120px | ImageSizeL1 = 120px
| ImageAltL1 = Skeletal formula of ''o''-anisidine
| IUPACName = 2-Methoxyaniline
| ImageFileR1 = O-Anisidine 3D ball.png
|OtherNames= 2-anisidine, ortho-aminoanisole, o-methoxyaniline, 2-methoxy-1-aminobenzene, 2-methoxyphenylamine
| ImageSizeR1 = 120
⚫ | Section1 = {{Chembox Identifiers
| ImageAltR1 = Ball-and-stick model of the ''o''-anisidine molecule
⚫ | InChI = 1/C7H9NO/c1-9-7-5-3-2-4-6(7)8/h2-5H,8H2,1H3
| PIN = 2-Methoxyaniline<ref name=iupac2013>{{cite book | title = Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book) | publisher = ] | date = 2014 | location = Cambridge | page = 669 | doi = 10.1039/9781849733069-00648 | isbn = 978-0-85404-182-4 | quote = The names ‘toluidine’, ‘anisidine’, and ‘phenetidine’ for which ''o''-, ''m''-, and ''p''- have been used to distinguish isomers, and ‘xylidine’ for which numerical locants, such as 2,3-, have been used, are no longer recommended, nor are the corresponding prefixes ‘toluidine’, ‘anisidino’, ‘phenetidine’, and ‘xylidino’.}}</ref>
⚫ | SMILES = Nc1ccccc1OC
| OtherNames = ''ortho''-Anisidine<br>2-Anisidine<br />''ortho''-Aminoanisole<br />''o''-Methoxyaniline<br />2-Methoxy-1-aminobenzene<br />2-Methoxyphenylamine
⚫ | StdInChI_Ref = {{stdinchicite|correct|chemspider}}
⚫ |Section1={{Chembox Identifiers
⚫ | InChI = 1/C7H9NO/c1-9-7-5-3-2-4-6(7)8/h2-5H,8H2,1H3
⚫ | SMILES = Nc1ccccc1OC
⚫ | StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C7H9NO/c1-9-7-5-3-2-4-6(7)8/h2-5H,8H2,1H3 | StdInChI = 1S/C7H9NO/c1-9-7-5-3-2-4-6(7)8/h2-5H,8H2,1H3
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| ChEBI = 82288
| StdInChIKey = VMPITZXILSNTON-UHFFFAOYSA-N | StdInChIKey = VMPITZXILSNTON-UHFFFAOYSA-N
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 1612004
| CASNo = 90-04-0 | CASNo = 90-04-0
| CASNo_Ref = {{cascite|correct|CAS}} | CASNo_Ref = {{cascite|correct|CAS}}
| EC-number = 201-963-1 | EC_number = 201-963-1
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 13860775 | ChemSpiderID = 13860775
| UNNumber = 2431 | UNNumber = 2431
| KEGG_Ref = {{keggcite|correct|kegg}} | KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = C19191 | KEGG = C19191
| PubChem = 7000
⚫ }}
| RTECS = BZ5410000
⚫ | Section2 = {{Chembox Properties
| UNII = NUX042F201
⚫ | Reference = <ref>{{RubberBible62nd|page=C-98}}.</ref>
⚫ }}
| Formula = C<sub>7</sub>H<sub>9</sub>NO
⚫ |Section2={{Chembox Properties
| MolarMass = 123.15 g/mol
⚫ | Properties_ref = <ref>{{RubberBible62nd|page=C-98}}</ref>
⚫ | Appearance= yellow liquid turns brown upon exposure to air
| Density = 1.092 g/ml | C=7 | H=9 | N=1 | O=1
⚫ | Appearance = Yellow liquid, turns brown upon exposure to air
| MeltingPt = 6.2 °C
| BoilingPt = 224 °C | MeltingPtC = 6.2
| Density = 1.0923 g/cm<sup>3</sup> | BoilingPtC = 224
| Density = 1.0923 g/cm<sup>3</sup>
| Solubility = 1.5 g/100 ml | Solubility = 1.5 g/100 ml
| SolubleOther = soluble in ], ], ], ] | SolubleOther = soluble in ], ], ], ]
| MagSus = -80.44·10<sup>−6</sup> cm<sup>3</sup>/mol
}} }}
| Section7 = {{Chembox Hazards |Section7={{Chembox Hazards
| EUClass = Toxic ('''T''')<br/>{{Carc2}}<br/>{{Muta3}}
| NFPA-H = 2
| EUIndex = 612-035-00-4
| NFPA-H = 2 | NFPA-F = 1
| NFPA-F = 1 | NFPA-R = 0
| NFPA-R = 0 | FlashPtC = 118
⚫ | FlashPt_notes = (open cup)
| RPhrases = {{R45}}, {{R23/24/25}}, {{R68}}
| AutoignitionPtC = 415
| SPhrases = {{S53}}, {{S45}}
| GHSPictograms = {{GHS06}}{{GHS08}}
⚫ | FlashPt = 118 °C (open cup)
| GHSSignalWord = Danger
| Autoignition = 415 °C
| HPhrases = {{H-phrases|301|311|331|341|350}}
⚫ }}
| PPhrases = {{P-phrases|201|202|261|264|270|271|280|281|301+310|302+352|304+340|308+313|311|312|321|322|330|361|363|403+233|405|501}}
⚫ | Section8 = {{Chembox Related
| PEL = TWA 0.5 mg/m<sup>3</sup> <ref name=NIOSH>{{PGCH|0034}}</ref>
⚫ | OtherCpds = ]<br/>]
| MainHazards = potential occupational carcinogen<ref name=NIOSH/>
⚫ }}
| IDLH = 50 mg/m<sup>3</sup><ref name=NIOSH/>
| REL = : Ca TWA 0.5 mg/m<sup>3</sup> <ref name=NIOSH/>
| LD50 = 2000 mg/kg (rat, oral)<br/> 1400 mg/kg (mouse, oral)<br/>870 mg/kg (rabbit, oral)<ref>{{IDLH|90040|''o''-Anisidine}}</ref>
⚫ }}
⚫ |Section8={{Chembox Related
⚫ | OtherCompounds = ]<br/>]
⚫ }}
}} }}


'''''o''-Anisidine''' ('''2-anisidine''') is an organic compound with the formula CH<sub>3</sub>OC<sub>6</sub>H<sub>4</sub>NH<sub>2</sub>. A colorless liquid, commercial samples can appear yellow owing to air oxidation. It is one of three isomers of the methoxy-containing ] derivative.
'''''o''-Anisidine''' is a yellow liquid with melting point -1 to 5 °C and density 1.09 g/cm³. The vapor pressure is 0.05 mbar at 20 °C but increases greatly with temperature. It has an aromatic smell and is well absorbed by inhalation, oral ingestion and skin contact. 2-Anisidine is a very toxic agent that causes blood, enzyme and nerve damage with ] and the danger of suffocation. The agent is an experimental ] and is strongly suspected to be also a human carcinogen. 2-Anisidine has dangerous pollutant properties for water.

==Production and use==
It is prepared via methanolysis of 2-chloronitrobenzene:<ref name=Booth>{{cite encyclopedia|author=Gerald Booth|chapter=Nitro Compounds, Aromatic|encyclopedia=Ullmann's Encyclopedia of Industrial Chemistry|year=2007|publisher=Wiley-VCH|location=Weinheim|doi=10.1002/14356007.a17_411|isbn=978-3527306732}}</ref>
:NaOCH<sub>3</sub> + ClC<sub>6</sub>H<sub>4</sub>NO<sub>2</sub> → CH<sub>3</sub>OC<sub>6</sub>H<sub>4</sub>NO<sub>2</sub> + NaCl
The resulting ] is reduced to ''o''-anisidine.

''o''-Anisidine is used in the manufacture of dyes. It is nitrated to give 4-nitroanisidine. It is also a precursor to ].

One special use is as a ] indicator. An acid solution of ''o''-anisidine is ] by adding a sodium nitrite solution. This mixture is applied to the wood and by reaction with ] in the heartwood a reddish brown ] is formed.

:] is an ] produced from ''o''-anisidine]]{{clear-left}}

==Safety and environmental aspects==
''o''-Anisidine is a dangerous pollutant from the production of dyes. It is listed as RCRA ], with the code K181.<ref>{{Cite web | url=http://www.epa.gov/osw/hazard/wastetypes/wasteid/dyes/index.htm | title=Hazardous Waste| date=2015-07-23}}</ref> The International Agency for Research on Cancer (IARC) has classified ''o''-anisidine as a Group 2B, possible human carcinogen.<ref>{{Cite web | url=https://pubchem.ncbi.nlm.nih.gov/compound/o-anisidine#section=Top |title = ''o''-Anisidine}}</ref>


==References== ==References==
Line 60: Line 91:
*{{PGCH|0034}} *{{PGCH|0034}}


{{DEFAULTSORT:Anisidine-2}} {{DEFAULTSORT:Anisidine, o-}}
] ]
] ]
] ]
]

Latest revision as of 20:15, 1 November 2024

o-Anisidine
Skeletal formula of o-anisidine
Ball-and-stick model of the o-anisidine molecule
Names
Preferred IUPAC name 2-Methoxyaniline
Other names ortho-Anisidine
2-Anisidine
ortho-Aminoanisole
o-Methoxyaniline
2-Methoxy-1-aminobenzene
2-Methoxyphenylamine
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.001.785 Edit this at Wikidata
EC Number
  • 201-963-1
KEGG
PubChem CID
RTECS number
  • BZ5410000
UNII
UN number 2431
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C7H9NO/c1-9-7-5-3-2-4-6(7)8/h2-5H,8H2,1H3Key: VMPITZXILSNTON-UHFFFAOYSA-N
  • InChI=1/C7H9NO/c1-9-7-5-3-2-4-6(7)8/h2-5H,8H2,1H3
SMILES
  • Nc1ccccc1OC
Properties
Chemical formula C7H9NO
Molar mass 123.155 g·mol
Appearance Yellow liquid, turns brown upon exposure to air
Density 1.0923 g/cm
Melting point 6.2 °C (43.2 °F; 279.3 K)
Boiling point 224 °C (435 °F; 497 K)
Solubility in water 1.5 g/100 ml
Solubility soluble in ethanol, diethyl ether, acetone, benzene
Magnetic susceptibility (χ) -80.44·10 cm/mol
Hazards
Occupational safety and health (OHS/OSH):
Main hazards potential occupational carcinogen
GHS labelling:
Pictograms GHS06: ToxicGHS08: Health hazard
Signal word Danger
Hazard statements H301, H311, H331, H341, H350
Precautionary statements P201, P202, P261, P264, P270, P271, P280, P281, P301+P310, P302+P352, P304+P340, P308+P313, P311, P312, P321, P322, P330, P361, P363, P403+P233, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2 1 0
Flash point 118 °C (244 °F; 391 K) (open cup)
Autoignition
temperature 		415 °C (779 °F; 688 K)
Lethal dose or concentration (LD, LC):
LD50 (median dose) 2000 mg/kg (rat, oral)
1400 mg/kg (mouse, oral)
870 mg/kg (rabbit, oral)
NIOSH (US health exposure limits):
PEL (Permissible) TWA 0.5 mg/m
REL (Recommended) : Ca TWA 0.5 mg/m
IDLH (Immediate danger) 50 mg/m
Related compounds
Related compounds m-Anisidine
p-Anisidine
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒N verify (what is  ?) Infobox references
Chemical compound

o-Anisidine (2-anisidine) is an organic compound with the formula CH3OC6H4NH2. A colorless liquid, commercial samples can appear yellow owing to air oxidation. It is one of three isomers of the methoxy-containing aniline derivative.

Production and use

It is prepared via methanolysis of 2-chloronitrobenzene:

NaOCH3 + ClC6H4NO2 → CH3OC6H4NO2 + NaCl

The resulting o-nitroanisole is reduced to o-anisidine.

o-Anisidine is used in the manufacture of dyes. It is nitrated to give 4-nitroanisidine. It is also a precursor to o-dianisidine.

One special use is as a heartwood indicator. An acid solution of o-anisidine is diazotized by adding a sodium nitrite solution. This mixture is applied to the wood and by reaction with polyphenols in the heartwood a reddish brown azo dye is formed.

Direct Blue 15 is an azo dye produced from o-anisidine

Safety and environmental aspects

o-Anisidine is a dangerous pollutant from the production of dyes. It is listed as RCRA hazardous waste, with the code K181. The International Agency for Research on Cancer (IARC) has classified o-anisidine as a Group 2B, possible human carcinogen.

References

  1. Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 669. doi:10.1039/9781849733069-00648. ISBN 978-0-85404-182-4. The names 'toluidine', 'anisidine', and 'phenetidine' for which o-, m-, and p- have been used to distinguish isomers, and 'xylidine' for which numerical locants, such as 2,3-, have been used, are no longer recommended, nor are the corresponding prefixes 'toluidine', 'anisidino', 'phenetidine', and 'xylidino'.
  2. Weast, Robert C., ed. (1981). CRC Handbook of Chemistry and Physics (62nd ed.). Boca Raton, Florida: CRC Press. p. C-98. ISBN 0-8493-0462-8.
  3. ^ NIOSH Pocket Guide to Chemical Hazards. "#0034". National Institute for Occupational Safety and Health (NIOSH).
  4. "o-Anisidine". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  5. Gerald Booth (2007). "Nitro Compounds, Aromatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_411. ISBN 978-3527306732.
  6. "Hazardous Waste". 2015-07-23.
  7. "o-Anisidine".

External links

Categories: