Skip to Content
Merck

I7512

Indole-3-butyric acid potassium salt

BioReagent, suitable for plant cell culture

Synonym(s):

4-(3-Indolyl)butanoic acid, IBA

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C12H12KNO2
CAS Number:
60096-23-3
Molecular Weight:
241.33
NACRES:
NA.72
PubChem Substance ID:
24896117
UNSPSC Code:
10171502
MDL number:
MFCD00058442
Quality level:
200

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

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

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

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)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000510243
0000510243
0000498029
0000498029
0000447197

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

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
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
Amy Midori James et al.
Plant physiology, 174(1), 154-171 (2017-03-30)
The accumulation of proanthocyanidins is regulated by a complex of transcription factors composed of R2R3 MYB, basic helix-loop-helix, and WD40 proteins that activate the promoters of biosynthetic genes. In poplar (genus
Rubini Kannangara et al.
Nature communications, 8(1), 1987-1987 (2017-12-08)
Carminic acid, a glucosylated anthraquinone found in scale insects like Dactylopius coccus, has since ancient times been used as a red colorant in various applications. Here we show that a membrane-bound C-glucosyltransferase, isolated from D. coccus and designated DcUGT2, catalyzes
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
View All Related Papers

Related Content

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