GLPBio

Indole-3-butyric acid-d 2

Catalog No.: GC80498Purity:>99.50%Synonyms: Indolebutyric acid-d 2
Indole-3-butyric acid -d 2 (Indolebutyric acid-d 2 ) is the deuterium labeled Indole-3-butyric acid.

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Indole-3-butyric acid-d 2
5mgIn Stock
$126.00
1
10mgIn Stock
$202.00
1
25mgIn Stock
$403.00
1

Zitate (Citations)

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    Nature
    641, 529–536 (2025)
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    628, 630–638 (2024)
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    632, 686–694 (2024)
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    Nature
    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
  • Cell cover
    Cell
    183(7):1867-1883 (2020)
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    Science
    388(6745) (2025)
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    387(6739) (2025)
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    387(6734) (2025)
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    35, 97–116 (2025)
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    34, 683–706 (2024)
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    33, 273–287 (2023)
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    33, 546–561 (2023)
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    33, 904–922 (2023)
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    31, 1291–1307 (2021)

Beschreibung (Description)

Indole-3-butyric acid -d 2 (Indolebutyric acid-d 2 ) is the deuterium labeled Indole-3-butyric acid. Indole-3-butyric acid (3-indolebutyric acid) is a plant growth auxin and a good rooting agent. It can promote herbs and woody ornamental plant rooting and used for improving fruit rate. Indole 3-butyric acid is an auxin precursor, and is converted to indole 3-acetic acid (IAA) in a peroxisomal β-oxidation process [1].

In Vitro, Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs.

References:
[1]. Damodaran S, Strader LC. Indole 3-Butyric Acid Metabolism and Transport in Arabidopsis thaliana. Front Plant Sci. 2019 Jul 3;10:851.
[2]. Fattorini L, et al. Indole-3-butyric acid promotes adventitious rooting in Arabidopsis thaliana thin cell layers by conversion into indole-3-acetic acid and stimulation of anthranilate synthase activity. BMC Plant Biol. 2017 Jul 11;17(1):121.
[3]. Schlicht M, et al. Indole-3-butyric acid induces lateral root formation via peroxisome-derived indole-3-acetic acid and nitric oxide. New Phytol. 2013 Oct;200(2):473-482.

Produktdokumente (Product Documents)

Purity:>99.50%Appearance:A solid

Chemische Eigenschaften (Chemical Properties)

Synonyme
Indolebutyric acid-d 2
Summenformel
C12H11D2NO2
Molekulargewicht
205.25
Löslichkeit
DMSO: 100 mg/mL (487.21 mM; Need ultrasonic)
Lagerung
Store at -20°C
Versandbedingungen
Evaluierungsmuster werden mit Kühlakkus versandt. Andere verfügbare Größen werden bei Raumtemperatur oder auf Anfrage mit Kühlakkus versandt.

Rechner (Calculators)Molarität / Verdünnung / Molekulargewicht / Einheitenumrechnung / In-vivo-Formulierung / Löslichkeit

g/mol

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