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133-32-4

133-32-4 structural image
Product Name: Indole-3-butyric acid
Formula: C12H13NO2
Synonyms: 4-(3-Indolyl)butanoic acid;4-(3-Indolyl)butyric acid;IBA
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CHEMICAL AND PHYSICAL PROPERTIES

Physical Description White or slightly yellow solid; [Merck Index] Off-white powder; [MSDSonline]
Color/Form White to slightly yellow crystals
Odor Essentially odorless
Melting Point 124.5 °C
Solubility 250 mg/L (at 20 °C)
Vapor Pressure 0.00000117 [mmHg]
LogP 2.3
Henry's Law Constant Henry's Law constant: 1.3X10-11 atm cu m/mol@ 25 °C /Estimated/
Stability/Shelf Life Very stable in neutral, acidic and alkaline media.
Dissociation Constants pKa = 4.7 /Estimated/
Kovats Retention Index 1885
Other Experimental Properties Hydroxyl radical reaction rate constant: 2.0X10-10 cu cm/molecule-sec @ 25 °C /Estimated/
Chemical Classes Pesticides -> Plant Growth Regulators

SAFETY INFORMATION

Signal word Danger
Pictogram(s)

Skull and Crossbones
Acute Toxicity
GHS06
GHS Hazard Statements H301:Acute toxicity,oral
Precautionary Statement Codes P264:Wash hands thoroughly after handling.
P264:Wash skin thouroughly after handling.
P270:Do not eat, drink or smoke when using this product.
P301+P310:IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P405:Store locked up.
P501:Dispose of contents/container to..…

COMPUTED DESCRIPTORS

Molecular Weight 203.24 g/mol
XLogP3 2.3
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 4
Exact Mass 203.094628657 g/mol
Monoisotopic Mass 203.094628657 g/mol
Topological Polar Surface Area 53.1 Ų
Heavy Atom Count 15
Formal Charge 0
Complexity 230
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
Covalently-Bonded Unit Count 1
Compound Is Canonicalized Yes

PRODUCT INTRODUCTION

description

Indole-3-butyric acid is a substance that is closely related in structure and function to a natural growth regulator found in plants. Indole-3-butyric acid is used on many crops and ornamentals to promote growth and development of roots, flowers and fruits, and to increase crop yields. Growers find it more effective and efficient than its natural counterpart because plants cannot break it down as quickly. No harm to humans or the environment is expected to result from use of indole-3-butyric acid.

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