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Merck

I5386

Indole-3-butyric acid

suitable for plant cell culture, BioReagent

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C12H13NO2
CAS Number:
133-32-4
Molecular Weight:
203.24
UNSPSC Code:
10171502
NACRES:
NA.72
PubChem Substance ID:
24896067
EC Number:
205-101-5
Beilstein/REAXYS Number:
171120
MDL number:
MFCD00005664
Form:
solid
Assay:
≥98% (TLC)

Key Documents

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InChI key

JTEDVYBZBROSJT-UHFFFAOYSA-N

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)

SMILES string

OC(=O)CCCc1c[nH]c2ccccc12

product line

BioReagent

assay

≥98% (TLC)

form

solid

technique(s)

cell culture | plant: suitable

application(s)

agriculture

storage temp.

2-8°C

Quality Level

200

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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

Preparation and Use

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

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

ppe

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

I5386-25G: + I5386-VAR: + I5386-1G: + I5386-BULK: + I5386-5G: + I5386-100MG:

jan

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Certificates of Analysis (COA)

Lot/Batch Number
0000527387
0000527387
0000508028
0000511521
0000508030

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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
Yi-Hsuan Chen et al.
Plant cell reports, 31(6), 1085-1091 (2012-01-21)
Lateral root (LR) development performs the essential tasks of providing water, nutrients, and physical support to plants. Therefore, understanding the regulation of LR development is of agronomic importance. In this study, we examined the effect of nitric oxide (NO), auxin
View All Related Papers

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