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I7512

Sigma-Aldrich

Indole-3-butyric acid potassium salt

suitable for plant cell culture, BioReagent

Synonym(s):

4-(3-Indolyl)butanoic acid, IBA

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About This Item

Empirical Formula (Hill Notation):
C12H12KNO2
CAS Number:
Molecular Weight:
241.33
MDL number:
UNSPSC Code:
10171502
PubChem Substance ID:
NACRES:
NA.72

product line

BioReagent

technique(s)

cell culture | plant: suitable

application(s)

agriculture

storage temp.

2-8°C

SMILES string

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

InChI

1S/C12H13NO2.K.H/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

RBRDCGZGWQSQJU-UHFFFAOYSA-N

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Application

Indole-3-butyric acid (IBA) is auxin-family plant hormone. 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.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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’.

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Jan M Schuller et al.
Science (New York, N.Y.), 363(6424), 257-260 (2018-12-24)
Photosynthetic complex I enables cyclic electron flow around photosystem I, a regulatory mechanism for photosynthetic energy conversion. We report a 3.3-angstrom-resolution cryo-electron microscopy structure of photosynthetic complex I from the cyanobacterium Thermosynechococcus elongatus. The model reveals structural adaptations that facilitate
Amy Midori James et al.
Plant physiology, 174(1), 154-171 (2017-03-30)
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Bozidar Casar et al.
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Nature communications, 8, 15858-15858 (2017-07-04)
The capacity of metal-containing porphyrinoids to mediate reductive dehalogenation is implemented in cobamide-containing reductive dehalogenases (RDases), which serve as terminal reductases in organohalide-respiring microbes. RDases allow for the exploitation of halogenated compounds as electron acceptors. Their reaction mechanism is under

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