Revision as of 21:05, 25 August 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'ChemSpiderID_Ref', 'DrugBank_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'ChEBI_Ref') per [[Misplaced Pages:WikiProject Chemicals/Chembox validati← Previous edit | Latest revision as of 01:11, 14 December 2024 edit undo2a00:23c5:fe1c:3701:e4f5:c417:56ac:aead (talk) grammar | ||
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{{Chembox | {{Chembox | ||
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⚫ | | verifiedrevid = |
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⚫ | | verifiedrevid = 446718238 | ||
| Name = 2-Tolidine | | Name = 2-Tolidine | ||
| Reference = <ref name="BGIA GESTIS">{{GESTIS|Name=ortho-Tolidin|ZVG=17950|CAS=119-93-7|Date=6.6.2008}}</ref> | | Reference = <ref name="BGIA GESTIS">{{GESTIS|Name=ortho-Tolidin|ZVG=17950|CAS=119-93-7|Date=6.6.2008}}</ref> | ||
| ImageFile = 2-tolidine.svg | | ImageFile = 2-tolidine.svg | ||
⚫ | | ImageAlt = | ||
| ImageSize = 200px | |||
| PIN = 3,3′-Dimethyl--4,4′-diamine | |||
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⚫ | | OtherNames = ''o''-Tolidine; Orthotolidine; Diaminoditolyl; Diaminotolyl; Bianisidine; Tolidine blue; 3,3'-Dimethylbenzidine; 4,4'-Bi-''o''-] | ||
| IUPACName = 4-(4-Amino-3-methylphenyl)-2-methylaniline | |||
⚫ | |Section1={{Chembox Identifiers | ||
⚫ | | OtherNames = ''o''-Tolidine; Orthotolidine; Diaminoditolyl; Diaminotolyl; Bianisidine; Tolidine blue; 3,3'-Dimethylbenzidine; 4,4'-Bi-''o''-toluidine | ||
| CASNo_Ref = {{cascite|correct|CAS}} | |||
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| CASNo = 119-93-7 | ||
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| ChEMBL = 85109 | ||
| UNII_Ref = {{fdacite|correct|FDA}} | |||
| UNII = 63HLO2IV6K | |||
| PubChem = 8413 | |||
| KEGG_Ref = {{keggcite|correct|kegg}} | | KEGG_Ref = {{keggcite|correct|kegg}} | ||
| KEGG = C14443 | | KEGG = C14443 | ||
| |
| SMILES = CC1=C(C=CC(=C1)C2=CC(=C(C=C2)N)C)N | ||
| InChI = 1/C14H16N2/c1-9-7-11(3-5-13(9)15)12-4-6-14(16)10(2)8-12/h3-8H,15-16H2,1-2H3 | |||
| InChIKey = NUIURNJTPRWVAP-UHFFFAOYAK | |||
| StdInChI_Ref = {{stdinchicite|changed|chemspider}} | |||
| StdInChI = 1S/C14H16N2/c1-9-7-11(3-5-13(9)15)12-4-6-14(16)10(2)8-12/h3-8H,15-16H2,1-2H3 | |||
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} | |||
| StdInChIKey = NUIURNJTPRWVAP-UHFFFAOYSA-N | |||
| ChEBI_Ref = {{ebicite|correct|EBI}} | |||
| ChEBI = 34320 | |||
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | |||
| ChemSpiderID = 8106 | |||
| EINECS = 204-358-0 | |||
}} | }} | ||
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|Section2={{Chembox Properties | ||
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| C=14 | H=16 | N=2 | ||
| |
| Appearance = White to reddish crystals or powder | ||
| |
| Density = 1.23 g/cm<sup>3</sup> | ||
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| MeltingPtC = 129 | ||
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| BoilingPtC = 300.5 | ||
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| Solubility = 1.3 g/L}} | ||
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|Section3={{Chembox Hazards | ||
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| MainHazards = potential carcinogen | ||
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| FlashPtC = 244 | ||
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| AutoignitionPtC = | ||
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| GHSPictograms = {{GHS07}}{{GHS08}}{{GHS09}} | ||
| GHSSignalWord = Danger | |||
| SPhrases = {{S53}} {{S45}} {{S61}} | |||
| HPhrases = {{H-phrases|302|350|411}} | |||
| PPhrases = {{P-phrases|201|202|264|270|273|281|301+312|308+313|330|391|405|501}} | |||
| IDLH = Ca | |||
| PEL = Handle with care | |||
| REL = Ca C 0.02 mg/m<sup>3</sup> | |||
}} | }} | ||
}} | }} | ||
'''2-Tolidine''' ('''orthotolidine''', '''o-tolidine'''; not to be confused with ]) is an organic compound with the chemical formula (C<sub>6</sub>H<sub>4</sub>(CH<sub>3</sub>)NH<sub>2</sub>)<sub>2</sub>. Several isomers are known; the 3-tolidine derivative is also important commercially. It is a colorless compound although commercial samples are often colored. It is slightly soluble in water. It forms ] with acids, such as the ], which is commercially available. | |||
'''Tolidine''' is a group of ]ic ]s, the most prevalent of which is 2-tolidine (''o''-tolidine). | |||
2-Tolidine can be produced by many ] from a ] derivative derived from ].<ref>Noller, Carl R.: ''Textbook of Organic Chemistry'', Springer Verlag, 1960</ref> | |||
==Chemistry== | |||
:(CH<sub>3</sub>C<sub>6</sub>H<sub>4</sub>)<sub>2</sub>N<sub>2</sub>H<sub>2</sub> → (C<sub>6</sub>H<sub>3</sub>(CH<sub>3</sub>)NH<sub>2</sub>)<sub>2</sub> | |||
2-Tolidine is slightly soluble in water (1.3 g/L) and has a melting point of 129 °C. It readily forms ] with acids, such as the ] which is commercially available. 2-Tolidine can be produced by a ] from a hydrazine derivative.<ref>Noller, Carl R.: ''Textbook of Organic Chemistry'', Springer Verlag, 1960</ref> | |||
==Uses== | ==Uses== | ||
2-Tolidine |
2-Tolidine ] is used mainly for dye production.<ref name=Ullmann1>K. Hunger. W. Herbst "Pigments, Organic" in ''Ullmann's Encyclopedia of Industrial Chemistry'', Wiley-VCH, Weinheim, 2012. {{doi|10.1002/14356007.a20_371}}</ref> 2-Tolidine is an intermediate for the production of soluble ]s and insoluble pigments used particularly in the textile, leather and paper industries. | ||
], a derivative of o-tolidine]] | |||
It is also used for the production of certain ]s. | |||
⚫ | 2-Tolidine |
||
] | |||
⚫ | 2-Tolidine was widely used as a reagent or indicator in analytical, clinical and forensic chemistry, such as in the analytical determination of gold, or determination of the ] level in ] water. | ||
==Safety== | ==Safety== | ||
2-Tolidine is toxic and possibly |
2-Tolidine is toxic and possibly ]ic. It is listed as an ], meaning it is "possibly carcinogenic to humans". Animal studies have shown that animals exposed to tolidine developed tumors in the liver, kidney, and mammary glands.<ref>{{cite web |url=https://www.cdc.gov/niosh/npg/npgd0618.html |title=CDC - NIOSH Pocket Guide to Chemical Hazards - o-Tolidine |website=www.cdc.gov}}</ref> | ||
{{clear|left}} | |||
==References== | ==References== | ||
<references/> | <references/> | ||
{{Authority control}} | |||
] | ] | ||
] | |||
] | |||
] |
Latest revision as of 01:11, 14 December 2024
Names | |
---|---|
Preferred IUPAC name 3,3′-Dimethyl--4,4′-diamine | |
Other names o-Tolidine; Orthotolidine; Diaminoditolyl; Diaminotolyl; Bianisidine; Tolidine blue; 3,3'-Dimethylbenzidine; 4,4'-Bi-o-toluidine | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.003.962 |
EC Number |
|
KEGG | |
PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
InChI
| |
SMILES
| |
Properties | |
Chemical formula | C14H16N2 |
Molar mass | 212.296 g·mol |
Appearance | White to reddish crystals or powder |
Density | 1.23 g/cm |
Melting point | 129 °C (264 °F; 402 K) |
Boiling point | 300.5 °C (572.9 °F; 573.6 K) |
Solubility in water | 1.3 g/L |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards | potential carcinogen |
GHS labelling: | |
Pictograms | |
Signal word | Danger |
Hazard statements | H302, H350, H411 |
Precautionary statements | P201, P202, P264, P270, P273, P281, P301+P312, P308+P313, P330, P391, P405, P501 |
Flash point | 244 °C (471 °F; 517 K) |
NIOSH (US health exposure limits): | |
PEL (Permissible) | Handle with care |
REL (Recommended) | Ca C 0.02 mg/m |
IDLH (Immediate danger) | Ca |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references |
2-Tolidine (orthotolidine, o-tolidine; not to be confused with o-toluidine) is an organic compound with the chemical formula (C6H4(CH3)NH2)2. Several isomers are known; the 3-tolidine derivative is also important commercially. It is a colorless compound although commercial samples are often colored. It is slightly soluble in water. It forms salts with acids, such as the hydrochloride, which is commercially available.
2-Tolidine can be produced by many benzidine rearrangement from a hydrazine derivative derived from 2-nitrotoluene.
- (CH3C6H4)2N2H2 → (C6H3(CH3)NH2)2
Uses
2-Tolidine aromatic amine is used mainly for dye production. 2-Tolidine is an intermediate for the production of soluble azo dyes and insoluble pigments used particularly in the textile, leather and paper industries.
It is also used for the production of certain elastomers.
2-Tolidine was widely used as a reagent or indicator in analytical, clinical and forensic chemistry, such as in the analytical determination of gold, or determination of the chlorine level in swimming pool water.
Safety
2-Tolidine is toxic and possibly carcinogenic. It is listed as an IARC Group 2B carcinogen, meaning it is "possibly carcinogenic to humans". Animal studies have shown that animals exposed to tolidine developed tumors in the liver, kidney, and mammary glands.
References
- Record of ortho-Tolidin in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 6.6.2008.
- Noller, Carl R.: Textbook of Organic Chemistry, Springer Verlag, 1960
- K. Hunger. W. Herbst "Pigments, Organic" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2012. doi:10.1002/14356007.a20_371
- "CDC - NIOSH Pocket Guide to Chemical Hazards - o-Tolidine". www.cdc.gov.