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Merck

I7512

Indole-3-butyric acid potassium salt

BioReagent, suitable for plant cell culture

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
NACRES:
NA.72
PubChem Substance ID:
UNSPSC Code:
10171502
MDL number:
Quality level:
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Product Name

Indole-3-butyric acid potassium salt, BioReagent, suitable for plant cell culture

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);;

SMILES string

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

InChI key

RBRDCGZGWQSQJU-UHFFFAOYSA-N

product line

BioReagent

technique(s)

cell culture | plant: suitable

application(s)

agriculture

storage temp.

2-8°C

Quality Level

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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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Jan M Schuller et al.
Science (New York, N.Y.), 363(6424), 257-260 (2018-12-24)
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Hongbo Guo et al.
Emerging infectious diseases, 23(2), 220-231 (2016-11-22)
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Bozidar Casar et al.
Zeitschrift fur medizinische Physik, 27(3), 232-242 (2017-03-25)
The influence of the Integral Quality Monitor (IQM) transmission detector on photon beam properties was evaluated in a preclinical phase, using data from nine participating centres: (i) the change of beam quality (beam hardening), (ii) the influence on surface dose
Carolijn Smids et al.
Infection, 45(1), 41-49 (2016-06-19)
The purpose of this study was to evaluate the diagnostic value of From January 2006 to August 2013 patients with a clinical suspicion of spondylodiscitis, with an infection, or with fever of unknown origin were retrospectively included if Sixty-eight patients
Cindy Kunze et al.
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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