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I5386

Sigma-Aldrich

Indole-3-butyric acid

BioReagent, suitable for plant cell culture

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Synonym(s):
4-(3-Indolyl)butanoic acid, 4-(3-Indolyl)butyric acid, IBA
Empirical Formula (Hill Notation):
C12H13NO2
CAS Number:
Molecular Weight:
203.24
Beilstein/REAXYS Number:
171120
EC Number:
MDL number:
PubChem Substance ID:

product line

BioReagent

technique(s)

cell culture | plant: suitable

application(s)

agriculture

storage temp.

2-8°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

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1 of 4

This Item
I7512573101.00354
vibrant-m

I5386

Indole-3-butyric acid

vibrant-m

57310

Indole-3-butyric acid

vibrant-m

1.00354

Indole-3-butyric acid

product line

BioReagent

product line

BioReagent

product line

-

product line

-

technique(s)

cell culture | plant: suitable

technique(s)

cell culture | plant: suitable

technique(s)

-

technique(s)

-

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

-

storage temp.

2-30°C

application(s)

agriculture

application(s)

agriculture

application(s)

-

application(s)

-

Application

Indole-3-butyric acid (IBA) is auxin-family plant hormone (phytohormone). IBA is thought to be a precursor of indole-3-acetic acid (IAA) the most abundant and the basic auxin natively occurring and functioning in plants. IAA generates the majority of auxin effects in intact plants, and is the most potent native auxin.

Preparation Note

related product

Product No.
Description
Pricing

pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Shengbin Liu et al.
Plant physiology (2021-10-19)
In cultivated grasses, tillering, leaf, and inflorescence architecture, as well as abscission ability, are major agronomical traits. In barley (Hordeum vulgare), maize (Zea mays), rice (Oryza sativa), and brachypodium (Brachypodium distachyon), NOOT-BOP-COCH-LIKE (NBCL) genes are essential regulators of vegetative and
Lucia C Strader et al.
Plant physiology, 153(4), 1577-1586 (2010-06-22)
Genetic evidence in Arabidopsis (Arabidopsis thaliana) suggests that the auxin precursor indole-3-butyric acid (IBA) is converted into active indole-3-acetic acid (IAA) by peroxisomal beta-oxidation; however, direct evidence that Arabidopsis converts IBA to IAA is lacking, and the role of IBA-derived
Fatima Naim et al.
PloS one, 15(1), e0227994-e0227994 (2020-01-25)
Introducing a new trait into a crop through conventional breeding commonly takes decades, but recently developed genome sequence modification technology has the potential to accelerate this process. One of these new breeding technologies relies on an RNA-directed DNA nuclease (CRISPR/Cas9)
Kamil Ruzicka et al.
Proceedings of the National Academy of Sciences of the United States of America, 107(23), 10749-10753 (2010-05-26)
Differential distribution of the plant hormone auxin within tissues mediates a variety of developmental processes. Cellular auxin levels are determined by metabolic processes including synthesis, degradation, and (de)conjugation, as well as by auxin transport across the plasma membrane. Whereas transport
Lucia C Strader et al.
Molecular plant, 4(3), 477-486 (2011-03-02)
Plant growth and morphogenesis depend on the levels and distribution of the plant hormone auxin. Plants tightly regulate cellular levels of the active auxin indole-3-acetic acid (IAA) through synthesis, inactivation, and transport. Although the transporters that move IAA into and

Protocols

Reference guide and preparation guide for antibiotic and antimycotic use in plant tissue culture.

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