Indole-3-acetic acid sodium salt (CAS 6505-45-9)
See product citations (10)
Alternate Names:
Indole-3-acetic acid sodium salt is also known as Heteroauxin.
Application:
Indole-3-acetic acid sodium salt is Indole-3-acetic acid induces cell division and cell elongation that promotes plant growth.
CAS Number:
6505-45-9
Purity:
>98%
Molecular Weight:
197.17
Molecular Formula:
C10H8NNaO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Indole-3-acetic acid sodium salt is a plant growth regulator and provides a useful standard for analysis of these growth pathways. It induces cell division and cell elongation that promotes plant growth. Indole-3-Acetic acid, also known as Heteroauxin, belongs to the auxin class of naturally occurring plant hormones. It exhibits growth inhibiting effects at high concentrations, including epinasty. Highly concentrated Indole-3-Acetic acid can also prevent "shoot and root" growth, the effects of which formed the basis for which synthetic auxins were developed as herbicides.
Indole-3-acetic acid sodium salt (CAS 6505-45-9) References
- Auxin-induced ethylene triggers abscisic acid biosynthesis and growth inhibition. | Hansen, H. and Grossmann, K. 2000. Plant Physiol. 124: 1437-48. PMID: 11080318
- Determination of uremic solutes in biological fluids of chronic kidney disease patients by HPLC assay. | Calaf, R., et al. 2011. J Chromatogr B Analyt Technol Biomed Life Sci. 879: 2281-6. PMID: 21727042
- Conversion L-tryptophan to melatonin in the gastrointestinal tract: the new high performance liquid chromatography method enabling simultaneous determination of six metabolites of L-tryptophan by native fluorescence and UV-VIS detection. | Zagajewski, J., et al. 2012. J Physiol Pharmacol. 63: 613-21. PMID: 23388477
- Pseudomonas aeruginosa uses T3SS to inhibit diabetic wound healing. | Goldufsky, J., et al. 2015. Wound Repair Regen. 23: 557-64. PMID: 25912785
- Regulated protein depletion by the auxin-inducible degradation system in Drosophila melanogaster. | Trost, M., et al. 2016. Fly (Austin). 10: 35-46. PMID: 27010248
- The Uremic Toxin Indoxyl-3-Sulfate Induces CYP1A2 In Primary Human Hepatocytes. | Liu, H., et al. 2016. Drug Metab Lett. 10: 195-199. PMID: 27449409
- Environmental Growth Conditions of Trichoderma spp. Affects Indole Acetic Acid Derivatives, Volatile Organic Compounds, and Plant Growth Promotion. | Nieto-Jacobo, MF., et al. 2017. Front Plant Sci. 8: 102. PMID: 28232840
- The Cohesin Ring Uses Its Hinge to Organize DNA Using Non-topological as well as Topological Mechanisms. | Srinivasan, M., et al. 2018. Cell. 173: 1508-1519.e18. PMID: 29754816
- Conditional control of fluorescent protein degradation by an auxin-dependent nanobody. | Daniel, K., et al. 2018. Nat Commun. 9: 3297. PMID: 30120238
- Uremic metabolites impair skeletal muscle mitochondrial energetics through disruption of the electron transport system and matrix dehydrogenase activity. | Thome, T., et al. 2019. Am J Physiol Cell Physiol. 317: C701-C713. PMID: 31291144
- Auxin-mediated rapid degradation of target proteins in hippocampal neurons. | Nakano, R., et al. 2019. Neuroreport. 30: 908-913. PMID: 31373971
- Cohesin-Dependent and -Independent Mechanisms Mediate Chromosomal Contacts between Promoters and Enhancers. | Thiecke, MJ., et al. 2020. Cell Rep. 32: 107929. PMID: 32698000
- Microtubules play a crucial role in regulating actin organization and cell initiation in cotton fibers. | Zeng, J., et al. 2022. Plant Cell Rep. 41: 1059-1073. PMID: 35217893
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Indole-3-acetic acid sodium salt, 2 g | sc-215171 | 2 g | $70.00 | |||
Indole-3-acetic acid sodium salt, 10 g | sc-215171A | 10 g | $252.00 | |||
Indole-3-acetic acid sodium salt, 100 g | sc-215171B | 100 g | $752.00 |