3-Indole-acetic acid sodium salt - ≥98% , CAS No.6505-45-9

CAS: 6505-45-9 Cat. No.: I276187 Peso molecular: 197.17 Número EC: 800-071-5

GRADE & PURITY ≥98%

Synonyms

SCHEMBL468235 | F20491 | Sodium 2-(1H-indol-3-yl)acetate | 1H-Indole-3-aceticacid,sodium salt(1:1) | 1H-Indole-3-acetic acid, monosodium salt | AS-64458 | sodium;2-(1H-indol-3-yl)acetate | HY-18569A | C10H8NNaO2 | AKOS016004419 | A867753 | Indole-3-acetic

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

Descripción general

Product Describtion:

3-Indole-acetic acid sodium salt is a plant growth regulator. Indole-3-acetic acid induces cell division and cell elongation that promotes plant growth.

Product Application:

3-Indole-acetic acid (IAA) sodium salt has been used:
to alter the root developmental processes in Arabidopsis thaliana seedlings；
as a standard for the determination of IAA by high-performance liquid chromatography using Chlorella sorokiniana and Azospirillum brasilense sample culture media；
as one of the plant hormone to treat interspecific hybrids (Elaeis oleifera Cortés x Elaeis guineensis Jacq.) and study its effect on bunch formation in parthenocarpic fruits and oil production in oil palm.

Specifications

Sinónimos

SCHEMBL468235 | F20491 | Sodium 2-(1H-indol-3-yl)acetate | 1H-Indole-3-aceticacid, sodium salt(1:1) | 1H-Indole-3-acetic acid, monosodium salt | AS-64458 | sodium;2-(1H-indol-3-yl)acetate | HY-18569A | C10H8NNaO2 | AKOS016004419 | A867753 | Indole-3-acetic

Especificaciones y pureza

≥98%

Mecanismos bioquímicos y fisiológicos

3-Indole-acetic acid (IAA), a plant hormone, belongs to the class of auxins. It is also synthesized by bacterial pathogens, fungi, and organisms that live in a symbiotic relationship with plants and algae. IAA induces the growth and development of the hos

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Protected from light

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504769617
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504769617
• Sonrisas canónicas: C1=CC=C2C(=C1)C(=CN2)CC(=O)[O-].[Na+]
• IUPAC Name: sodium;2-(1H-indol-3-yl)acetate
• InChIKey: YGSPWCVTJRFZEL-UHFFFAOYSA-M
• INCHI: 1S/C10H9NO2.Na/c12-10(13)5-7-6-11-9-4-2-1-3-8(7)9;/h1-4,6,11H,5H2,(H,12,13);/q;+1/p-1
• Isómeros SMILES: C1=CC=C2C(=C1)C(=CN2)CC(=O)[O-].[Na+]
• Peso molecular: 197.17
• Reaxy-Rn: 8092878
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8092878&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Indoles and derivatives
      • Subclass Indolyl carboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Indoles and derivatives
• Subclass: Indolyl carboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Indole-3-acetic acid derivatives
• Alternative Parents: 3-alkylindoles Substituted pyrroles Benzenoids Heteroaromatic compounds Carboxylic acid salts Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organonitrogen compounds Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic cations
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Indole-3-acetic acid derivative - 3-alkylindole - Indole - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Carboxylic acid salt - Carboxylic acid derivative - Azacycle - Organic alkali metal salt - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxide - Carbonyl group - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic salt - Organic sodium salt - Hydrocarbon derivative - Organic cation - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as indole-3-acetic acid derivatives. These are compounds containing an acetic acid (or a derivative) linked to the C3 carbon atom of an indole.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Solubilidad: H2O: soluble
• Peso molecular: 197.170 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 197.045 Da
• Monoisotopic Mass: 197.045 Da
• Topological Polar Surface Area: 55.900 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 210.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

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