WARNING: This product is for research use only, not for human or veterinary use.
Hodoodo CAT#: H596222
CAS#: 133-32-4
Description: 4-Indol-3-ylbutyric acid is a naturally occurring phytohormone auxin (plant growth regulator). Promotes root formation in cuttings, but does not affect ethylene levels.
Hodoodo Cat#: H596222
Name: 4-Indol-3-ylbutyric acid
CAS#: 133-32-4
Chemical Formula: C12H13NO2
Exact Mass: 203.09
Molecular Weight: 203.240
Elemental Analysis: C, 70.92; H, 6.45; N, 6.89; O, 15.74
Synonym: 4-Indol-3-ylbutyric acid; EPA Pesticide Chemical Code 046701; Indolbutyric acid; Hormodin; NSC 3130; NSC3130; NSC-3130;
IUPAC/Chemical Name: 4-(1H-indol-3-yl)butanoic acid
InChi Key: JTEDVYBZBROSJT-UHFFFAOYSA-N
InChi Code: 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)
SMILES Code: O=C(O)CCCC1=CNC2=C1C=CC=C2
Appearance: Solid powder
Purity: >98% (or refer to the Certificate of Analysis)
Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility: Soluble in DMSO
Shelf Life: >2 years if stored properly
Drug Formulation: This drug may be formulated in DMSO
Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code: 2934.99.9001
More Info:
| Biological target: | |
| In vitro activity: | |
| In vivo activity: |
The following data is based on the product molecular weight 203.24 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 1.15 mL | 5.76 mL | 11.51 mL |
| 5 mM | 0.23 mL | 1.15 mL | 2.3 mL |
| 10 mM | 0.12 mL | 0.58 mL | 1.15 mL |
| 50 mM | 0.02 mL | 0.12 mL | 0.23 mL |
| Formulation protocol: | |
| In vitro protocol: | |
| In vivo protocol: |
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8: Quan J, Meng S, Guo E, Zhang S, Zhao Z, Yang X. De novo sequencing and comparative transcriptome analysis of adventitious root development induced by exogenous indole-3-butyric acid in cuttings of tetraploid black locust. BMC Genomics. 2017 Feb 16;18(1):179. doi: 10.1186/s12864-017-3554-4. PubMed PMID: 28209181; PubMed Central PMCID: PMC5314683.
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13: Jásik J, Bokor B, Stuchlík S, Mičieta K, Turňa J, Schmelzer E. Effects of Auxins on PIN-FORMED2 (PIN2) Dynamics Are Not Mediated by Inhibiting PIN2 Endocytosis. Plant Physiol. 2016 Oct;172(2):1019-1031. Epub 2016 Aug 9. PubMed PMID: 27506239; PubMed Central PMCID: PMC5047079.
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15: Anjum S, Abbasi BH. Biomimetic synthesis of antimicrobial silver nanoparticles using in vitro-propagated plantlets of a medicinally important endangered species: Phlomis bracteosa. Int J Nanomedicine. 2016 Apr 22;11:1663-75. doi: 10.2147/IJN.S105532. eCollection 2016. PubMed PMID: 27217745; PubMed Central PMCID: PMC4853015.
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