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2-Methylindole-3-acetic acid

Base Information Edit
  • Chemical Name:2-Methylindole-3-acetic acid
  • CAS No.:1912-43-2
  • Molecular Formula:C11H11NO2
  • Molecular Weight:189.214
  • Hs Code.:2933990090
  • DSSTox Substance ID:DTXSID90343337
  • Nikkaji Number:J703.166A
  • Wikidata:Q72491863
  • ChEMBL ID:CHEMBL312858
  • Mol file:1912-43-2.mol
2-Methylindole-3-acetic acid

Synonyms:2-Methylindole-3-acetic acid;1912-43-2;2-(2-methyl-1H-indol-3-yl)acetic acid;(2-Methyl-1H-indol-3-yl)acetic acid;2-Methyl-3-indoleacetic acid;1H-Indole-3-acetic acid, 2-methyl-;MFCD00075006;2-(2-methyl-1~{H}-indol-3-yl)ethanoic acid;2-Methylindole-3-aceticacid;SMR000036607;2-Me-IAA;Oprea1_079937;MLS000039417;SCHEMBL379103;2-methyl-idole-3-acetic acid;2-Methylindole-3- acetic acid;CHEMBL312858;(2-methyl-3-indolyl)acetic acid;DTXSID90343337;CHEBI:182632;HMS2462J09;2-methyl-1h-indole-3-acetic acid;AMY25853;BCP27439;(2-Methyl-indol-3-yl)-acetic acid;BBL012863;STK119955;2-Methyl-3-indoleacetic acid, 98%;AKOS000113538;AC-6734;CS-W015941;FS-2263;(2-Methyl-1H-indol-3-yl)acetic acid #;A4222;FT-0613059;EN300-31810;M-3960;AN-666/13378006;SR-01000397827;Q-102907;SR-01000397827-1;Z335447192;QN5

Suppliers and Price of 2-Methylindole-3-acetic acid
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • 2-Methylindole-3-acetic acid
  • 5g
  • $ 433.00
  • TRC
  • 2-Methylindole-3-aceticAcid
  • 2.5g
  • $ 80.00
  • Sigma-Aldrich
  • 2-Methyl-3-indoleacetic acid 98%
  • 5g
  • $ 104.00
  • Matrix Scientific
  • (2-Methyl-1H-indol-3-yl)acetic acid
  • 500mg
  • $ 10.00
  • Crysdot
  • 2-Methylindole-3-aceticacid 95+%
  • 100g
  • $ 459.00
  • Chemenu
  • 2-Methylindole-3-aceticacid 95%
  • 100g
  • $ 434.00
  • American Custom Chemicals Corporation
  • 2-METHYL INDOLE-3-ACETIC ACID 95.00%
  • 50G
  • $ 2673.83
  • Ambeed
  • 2-Methylindole-3-aceticacid 98%
  • 10g
  • $ 59.00
  • Ambeed
  • 2-Methylindole-3-aceticacid 98%
  • 5g
  • $ 33.00
  • Ambeed
  • 2-Methylindole-3-aceticacid 98%
  • 1g
  • $ 10.00
Total 83 raw suppliers
Chemical Property of 2-Methylindole-3-acetic acid Edit
Chemical Property:
  • Melting Point:205 °C (dec.)(lit.) 
  • Boiling Point:418.158 °C at 760 mmHg 
  • PKA:4.19±0.30(Predicted) 
  • Flash Point:206.695 °C 
  • PSA:53.09000 
  • Density:1.3 g/cm3 
  • LogP:2.10340 
  • Storage Temp.:2-8°C(protect from light) 
  • Solubility.:DMSO (Slightly), Methanol (Slightly) 
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:189.078978594
  • Heavy Atom Count:14
  • Complexity:229
Purity/Quality:

98%,99%, *data from raw suppliers

2-Methylindole-3-acetic acid *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Safety Statements: 22-24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=C(C2=CC=CC=C2N1)CC(=O)O
  • Uses 2-Methylindole-3-acetic Acid is a derivative of Indole-3-acetic acid which is a plant growth regulator. It induces cell division and cell elongation that promotes plant growth.
Technology Process of 2-Methylindole-3-acetic acid

There total 23 articles about 2-Methylindole-3-acetic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With hydrogenchloride; acetic acid; for 4h; Heating;
DOI:10.1002/jlac.198319831010
Guidance literature:
With acetic acid; for 4h; Reflux;
DOI:10.3184/174751916X14737735069962
Guidance literature:
With zinc(II) chloride; at 140 ℃; Behandeln des entstandenen Aethylesters mit alkoh. Kalilauge;
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