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Quality Level
Assay
98%
form
powder
mp
205 °C (dec.) (lit.)
SMILES string
Cc1[nH]c2ccccc2c1CC(O)=O
InChI
1S/C11H11NO2/c1-7-9(6-11(13)14)8-4-2-3-5-10(8)12-7/h2-5,12H,6H2,1H3,(H,13,14)
InChI key
QJNNHJVSQUUHHE-UHFFFAOYSA-N
Related Categories
General description
2-Methyl-3-indoleacetic acid is a common plant growth hormone. Relative activity of 2-methyl-3-indoleacetic acid in promoting growth (elongation) in plant cells was evaluated.
Application
- Reactant for preparation of N-methyl-N-[[(nitrophenyl)sulfonyl]oxy]indoleacetamide derivatives
- Reactant for preparation of indomethacin analogs and derivatives
- Reactant for coupling reaction with diazomethane
- Reactant for prepnaration of (methylindolyl)methyltriazolethiones and (methylindolyl)methylthiadiazolylamines as antidepressant/anticonvulsant agents
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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On the Mechanism of Action of Growth Regulators.
Plant physiology, 28(2), 218-232 (1953-04-01)
Advances in the catalytic production of valuable levulinic acid derivatives.
ChemCatChem, 4(9), 1230-1237 (2012)
Electrophoresis, 41(3-4), 183-193 (2019-12-19)
In this paper, the development of a simple dilute-and-shoot method for quantifying urinary creatinine by CE-ESI-MS was described. The creatinine analysis time was about 7 min/sample by conventional single injection (SI) method and can be significantly reduced to less than 2 min/sample
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