Skip to the beginning of the images gallery

Indole-3-butyric acid potassium salt - 95%, high purity , CAS No.60096-23-3

1 Citations

COA

Grade & Purity:

≥95%

Cas Number: 60096-23-3
Molecular Weight: 241.3
PubChem CID: 23664348
PubChem SID: 504769491

In stock

Item Number

I185489

Grouped product items
SKU	Size	Availability	Price
I185489-5g	5g	3	$12.90
I185489-10g	10g	2	$19.90
I185489-25g	25g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$38.90
I185489-100g	100g	2	$136.90
I185489-500g	500g	1	$615.90

Water soluble auxin-family plant hormone.

View related series

Metabolite (5307)

Basic Description

Synonyms	Indole-3-butyric acid potassium salt \| Indole-3-butyric acid, potassium salt \| SY033643 \| indole-3-butyric acid-potassium salt \| AS-16118 \| potassium;4-(1H-indol-3-yl)butanoate \| 4-indol-3-ylbutanoic acid, potassium salt \| INDOLE-3-BUTYRIC ACID POTASSIUM
Specifications & Purity	≥95%
Biochemical and Physiological Mechanisms	Water soluble auxin-family plant hormone. Thought to be a precursor of indole-3-acetic acid (IAA) the most abundant and the basic auxin natively occurring and functioning in plants. IAA generates the majority of auxin effects in intact plants, and is the
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Note	Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Toxic, refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Indoles and derivatives
    - Subclass Indoles

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Indoles and derivatives
Subclass	Indoles
Intermediate Tree Nodes	Not available
Direct Parent	3-alkylindoles
Alternative Parents	Substituted pyrroles Benzenoids Heteroaromatic compounds Carboxylic acid salts Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organonitrogen compounds Organic potassium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic cations
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	3-alkylindole - Substituted pyrrole - Benzenoid - Pyrrole - Heteroaromatic compound - Carboxylic acid salt - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Organic alkali metal salt - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic salt - Organic potassium salt - Carbonyl group - Organic cation - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as 3-alkylindoles. These are compounds containing an indole moiety that carries an alkyl chain at the 3-position.
External Descriptors	Not available
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

Names and Identifiers

Pubchem Sid	504769491
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504769491
IUPAC Name	potassium;4-(1H-indol-3-yl)butanoate
INCHI	InChI=1S/C12H13NO2.K/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);/q;+1/p-1
InChIKey	KTWDHJYSJOSTSJ-UHFFFAOYSA-M
Smiles	C1=CC=C2C(=C1)C(=CN2)CCCC(=O)[O-].[K+]
Isomeric SMILES	C1=CC=C2C(=C1)C(=CN2)CCCC(=O)[O-].[K+]
Molecular Weight	241.3
Reaxy-Rn	31520089
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=31520089&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot Number	Certificate Type	Date	Item
L2417209	Certificate of Analysis	Dec 26, 2024	I185489
A2006178	Certificate of Analysis	Oct 07, 2023	I185489

Chemical and Physical Properties

Molecular Weight	241.330 g/mol
XLogP3
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	4
Exact Mass	241.051 Da
Monoisotopic Mass	241.051 Da
Topological Polar Surface Area	55.900 Å²
Heavy Atom Count	16
Formal Charge	0
Complexity	235.000
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

Documents & Articles

Solution Calculators

Molarity Calculator

Determine the necessary mass, volume, or concentration for preparing a solution.

Mass

Concentration

Volume

M. Wt*

g/mol

*When preparing stock solutions, always use the batch-specific molecular weight of the product found on the vial label and the Certificate of Analysis (available online).

Dilution Calculator

Determine the dilution needed to prepare a stock solution.

Concentration 1 (C1)

Volume 1 (V1)

Concentration 2 (C2)

Volume 2 (V2)

Reconstitution Calculator

The reconstitution calculator enables you to quickly determine the volume of a reagent needed to reconstitute your vial. Just enter the mass of the reagent and the target concentration, and the calculator will do the rest.

Volume (to add to vial)

Mass (in vial)

Desired Reconstitution Concentration