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Merck

45532

Supelco

Ácido indol-3-butírico

PESTANAL®, analytical standard

Sinónimos:

IBA, Ácido 4-(3-indolil)butanoico, Ácido 4-(3-indolil)butírico

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About This Item

Fórmula empírica (notación de Hill):
C12H13NO2
Número de CAS:
Peso molecular:
203.24
Beilstein/REAXYS Number:
171120
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

OC(=O)CCCc1c[nH]c2ccccc12

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)

InChI key

JTEDVYBZBROSJT-UHFFFAOYSA-N

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General description

Indole-3-butyric acid is a plant hormone in the auxin family[1] and is widely used in agriculture since it induces rooting[2] in various plants species such as mung bean (Vigna radiata L.) cuttings.[1]

Application

Indole-3-butyric acid may be used as a reference standard in the determination of indole-3-butyric acid in mung bean sprouts using high performance liquid chromatography with chemiluminescence (CL) detection.[3]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


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Certificados de análisis (COA)

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Los clientes también vieron

Genetic analysis of indole-3-butyric acid responses in Arabidopsis thaliana reveals four mutant classes.
Zolman KB, et al.
Genetics, 156(3), 1323-1337 (2000)
Determination of indole-3-acetic acid and indole-3-butyric acid in mung bean sprouts using high performance liquid chromatography with immobilized ru (bpy) 32+-kmno4 chemiluminescence detection.
Xi Z, et al.
Talanta, 79(2), 216-221 (2009)
Comparison of movement and metabolism of indole-3-acetic acid and indole-3-butyric acid in mung bean cuttings.
Wiesman Z, et al.
Physiologia Plantarum, 74(3), 556-560 (1988)
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Chemosphere, 84(2), 213-219 (2011-05-17)
Exogenous application of plant-growth promoting substances may potentially improve phytoremediation of metal-polluted substrates by increasing shoot and root growth. In a pot-based study, fodder radish (Raphanus sativus L. var. oleiformis Pers.) was grown in As-Zn-Cu-Co-Pb-contaminated pyrite waste, and treated with
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Analytical chemistry, 84(18), 7721-7728 (2012-08-30)
The conserved nucleotide binding site (NBS), found within the Fab variable domain of antibodies, remains a not-so-widely known and underutilized site. Here we describe a novel affinity chromatography method that utilizes the NBS as a target for selectively purifying antibodies

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