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Indole-3-butyric acid (potassium)

Indole-3-butyric acid (Indolebutyric acid) potassium is a plant growth auxin and a good rooting agent. It can promote herbs and woody ornamental plant rooting and used for improving fruit rate. Indole 3-butyric acid potassium is an auxin precursor, and is converted to indole 3-acetic acid (IAA) in a peroxisomal β-oxidation process[1].

Product Specifications

CAS Number

[60096-23-3]

Product Name Alternative

Indolebutyric acid (potassium)

UNSPSC

12352005

Hazard Statement

H302, H315, H319, H335

Target

Endogenous Metabolite

Type

Reference compound

Related Pathways

Metabolic Enzyme/Protease

Field of Research

Others

Assay Protocol

https://www.medchemexpress.com/indole-3-butyric-acid-potassium.html

Purity

99.77

Solubility

DMSO : 25 mg/mL (ultrasonic) |H2O : 100 mg/mL (ultrasonic)

Smiles

O=C(O[K])CCCC1=CNC2=C1C=CC=C2

Molecular Formula

C12H12KNO2

Molecular Weight

241.33

Precautions

H302, H315, H319, H335

References & Citations

[1]Damodaran S, Strader LC. Indole 3-Butyric Acid Metabolism and Transport in Arabidopsis thaliana. Front Plant Sci. 2019 Jul 3;10:851.|[2]Fattorini L, et al. Indole-3-butyric acid promotes adventitious rooting in Arabidopsis thaliana thin cell layers by conversion into indole-3-acetic acid and stimulation of anthranilate synthase activity. BMC Plant Biol. 2017 Jul 11;17 (1) :121.|[3]Schlicht M, et al. Indole-3-butyric acid induces lateral root formation via peroxisome-derived indole-3-acetic acid and nitric oxide. New Phytol. 2013 Oct;200 (2) :473-482.

Shipping Conditions

Room Temperature

Storage Conditions

Store at room temperature, keep dry and cool

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

Microbial Metabolite

Available Sizes

Curated Selection

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