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Merck
CN

I7512

Sigma-Aldrich

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:
60096-23-3
Molecular Weight:
241.33
MDL number:
MFCD00058442
UNSPSC Code:
10171502
PubChem Substance ID:
24896117
NACRES:
NA.72

Key Documents

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product line

BioReagent

Quality Level

200

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000498029
0000498029
0000447197
0000447197
0000403515

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Cindy Kunze et al.
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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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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
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Theranostics, 9(2), 554-572 (2019-02-28)
Heat shock protein 90 is an ATP-dependent molecular chaperone important for folding, maturation and clearance of aberrantly expressed proteins and is abundantly expressed (1-2% of all proteins) in the cytosol of all normal cells. In some tumour cells, however, strong
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
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
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