Skip to Content
Merck
All Photos(4)

Key Documents

View All Documentation

57310

Sigma-Aldrich

Indole-3-butyric acid

≥98.0% (T)

Synonym(s):

4-(3-Indolyl)butanoic acid, 4-(3-Indolyl)butyric acid, IBA

Sign Into View Organizational & Contract Pricing
All Photos(4)

About This Item

Empirical Formula (Hill Notation):
C12H13NO2
CAS Number:
133-32-4
Molecular Weight:
203.24
Beilstein:
171120
EC Number:
205-101-5
MDL number:
MFCD00005664
UNSPSC Code:
12352106
PubChem Substance ID:
57651621
NACRES:
NA.77

Quality Level

100

Assay

≥98.0% (T)

mp

122-125 °C

SMILES string

OC(=O)CCCc1c[nH]c2ccccc12

InChI

1S/C12H13NO2/c14-12(15)7-3-4-9-8-13-11-6-2-1-5-10(9)11/h1-2,5-6,8,13H,3-4,7H2,(H,14,15)

InChI key

JTEDVYBZBROSJT-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Indole-3-butyric acid (IBA) has been used as a standard to monitor IBA in urine samples by tandem mass spectrometry-selected reaction monitoring (SRM) and Ultra-high performance liquid chromatography (UHPLC), as a standard for high performance liquid chromatography (HPLC) for the quantification of IBA in foliar tissues of Coffea canephora seedlings.

Biochem/physiol Actions

Indole-3-butyric acid (IBA) is a naturally occurring phytohormone auxin (plant growth regulator). It promotes root formation in cuttings but does not affect ethylene levels. IBA might be a precursor for indole-3-acetic acid (IAA) through β oxidation pathway. IBA is present in plant species like Zea mays, Pisum sativum and Arabidopsis. IBA is more potent than IAA for inducing root formation.

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Transport of the two natural auxins, indole-3-butyric acid and indole-3-acetic acid, in Arabidopsis
Rashotte AM, et al.
Plant Physiology, 133(2), 761-772 (2003)
Dynamics of the concentration of IAA and some of its conjugates during the induction of somatic embryogenesis in Coffea canephora
Ayil-Gutierrez B, et al.
Plant signaling & behavior, 8(11), e26998-e26998 (2013)
K W Mudge et al.
Plant physiology, 61(2), 271-273 (1978-02-01)
Light-grown mung bean (Phaseolus aureus Roxb.) cuttings were treated with buffered and nonbuffered solutions of Ethephon, indole butyric acid (IBA), and the combination of both. Ethephon treatment resulted in increased tissue ethylene levels with increasing solution pH, but had no
Joohyun Kang et al.
Proceedings of the National Academy of Sciences of the United States of America, 107(5), 2355-2360 (2010-02-06)
Abscisic acid (ABA) is a ubiquitous phytohormone involved in many developmental processes and stress responses of plants. ABA moves within the plant, and intracellular receptors for ABA have been recently identified; however, no ABA transporter has been described to date.
Tereza Pavlova et al.
Analytica chimica acta, 987, 72-80 (2017-09-17)
While over 10% of the human metabolome is directly associated with the gut microbial metabolism, specific metabolites are largely uncharacterized. Therefore, methods for the identification and quantification of microbiota-associated metabolites in biological fluids such as urine or plasma are necessary
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service