Indole-3-butyric acid
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Indole-3-butyric acid | |
---|---|
General | |
Systematic name | 1H-Indole-3-butanoic acid |
Other names | indole-3-butyric acid 3-indolebutyric acid |
Molecular formula | C12H13NO2 |
SMILES | OC(CCCC2=CNC1=CC=CC=C12)=O |
Molar mass | 203.24 g/mol |
Appearance | white to light yellow crystals |
CAS number | [133-32-4] |
Properties | |
Density and phase | ? g/cm3 (20 °C), ? |
Solubility in water | ? g/100 ml (? °C) |
Melting point | 125 °C |
Boiling point | decomposes |
Acidity (pKa) | ? |
Basicity (pKb) | ? |
Chiral rotation [α]D | achiral |
Viscosity | ? cP at ? °C |
Structure | |
Crystal structure | ? cubic |
Dipole moment | ? D |
Hazards | |
MSDS | External MSDS |
Main hazards | |
NFPA 704 | |
Flash point | ? °C |
R/S statement | R: R25 R36/37/38 S: S26 S28 S36/37/39 S38 S45 |
RTECS number | NL5250000 |
Related compounds | |
Related | auxin indole-3-acetic acid |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
Indole-3-butyric acid (1H-Indole-3-butanoic acid, IBA) is a white to light-yellow crystalline solid, with the molecular formula C12H13NO2. It melts at 125 °C in atmospheric pressure and decomposes before boiling.
[edit] As a Plant Hormone
IBA is a plant hormone in the auxin family and is an ingredient in many commercial plant rooting horticultural products.
For use as such, it should be dissolved in about 75% (or purer) alcohol (as IBA does not dissolve in water), until a concentration from between 10,000 ppm to 50,000 ppm is achieved - this solution should then be diluted to the required concentration using distilled water. The solution should be kept in a cool, dark place for best results.
This compound had been thought to be strictly synthetic; however, it was reported that the compounds was isolated from leaves and seeds of maize and other species(Hopkins 1999).
[edit] References
- William. G.Hopkins(1999). Introduction to Plant Physiology. John Wiley and Sons. ISBN:0-471-19281-3
- Super-Grow website
- Oxford University Chemistry website