4-Ethoxybenzoic acid
featured

    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 592023

CAS#: 619-86-3

Description: 4-Ethoxybenzoic acid is a luminescent bioapplication.


Chemical Structure

img
4-Ethoxybenzoic acid
CAS# 619-86-3

Theoretical Analysis

MedKoo Cat#: 592023
Name: 4-Ethoxybenzoic acid
CAS#: 619-86-3
Chemical Formula: C9H10O3
Exact Mass: 166.06
Molecular Weight: 166.180
Elemental Analysis: C, 65.05; H, 6.07; O, 28.88

Price and Availability

Size Price Availability Quantity
25g USD 240 2 Weeks
Bulk inquiry

Synonym: 4-Ethoxybenzoic acid; NSC 8705; NSC8705; NSC-8705

IUPAC/Chemical Name: 4-Ethoxybenzoic acid

InChi Key: SHSGDXCJYVZFTP-UHFFFAOYSA-N

InChi Code: InChI=1S/C9H10O3/c1-2-12-8-5-3-7(4-6-8)9(10)11/h3-6H,2H2,1H3,(H,10,11)

SMILES Code: O=C(O)C1=CC=C(OCC)C=C1

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: >3 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: 2934.99.03.00

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 166.18 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.

Recalculate based on batch purity %
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:

Molarity Calculator

Calculate the mass, volume, or concentration required for a solution.
=
x
x
g/mol

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

Reconstitution Calculator

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.

=
÷

Dilution Calculator

Calculate the dilution required to prepare a stock solution.
x
=
x

1: Runowski M, Ekner-Grzyb A, Mrówczyńska L, Balabhadra S, Grzyb T, Paczesny J, Zep A, Lis S. Synthesis and organic surface modification of luminescent, lanthanide-doped core/shell nanomaterials (LnF3@SiO2@NH2@organic acid) for potential bioapplications: spectroscopic, structural, and in vitro cytotoxicity evaluation. Langmuir. 2014 Aug 12;30(31):9533-43. doi: 10.1021/la501107a. Epub 2014 Jul 30. PubMed PMID: 25036848.

2: Wang Y, Kim JH, Baek JB, Miller GW, Pennell KD. Transport behavior of functionalized multi-wall carbon nanotubes in water-saturated quartz sand as a function of tube length. Water Res. 2012 Sep 15;46(14):4521-31. doi: 10.1016/j.watres.2012.05.036. Epub 2012 May 30. PubMed PMID: 22704927; PubMed Central PMCID: PMC3395080.

3: Kumar NA, Jeon IY, Sohn GJ, Jain R, Kumar S, Baek JB. Highly conducting and flexible few-walled carbon nanotube thin film. ACS Nano. 2011 Mar 22;5(3):2324-31. doi: 10.1021/nn103630y. Epub 2011 Mar 3. PubMed PMID: 21370892.

4: Bolling BW, Parkin KL. Phenolic derivatives from soy flour ethanol extract are potent in vitro quinone reductase (QR) inducing agents. J Agric Food Chem. 2008 Nov 26;56(22):10473-80. doi: 10.1021/jf801541t. PubMed PMID: 18956872.

5: Matsuzaki F, Wariishi H. Functional diversity of cytochrome P450s of the white-rot fungus Phanerochaete chrysosporium. Biochem Biophys Res Commun. 2004 Nov 5;324(1):387-93. PubMed PMID: 15465031.

6: Niedan V, Pavasars I, Oberg G. Chloroperoxidase-mediated chlorination of aromatic groups in fulvic acid. Chemosphere. 2000 Sep;41(5):779-85. PubMed PMID: 10834381.

7: Middleton RE, Strnad NP, Cohen JB. Photoaffinity labeling the torpedo nicotinic acetylcholine receptor with [(3)H]tetracaine, a nondesensitizing noncompetitive antagonist. Mol Pharmacol. 1999 Aug;56(2):290-9. PubMed PMID: 10419547.

8: Stubbins JF, Pearson C, Qureshi GD. Inhibition of platelet aggregation by an irreversible local anesthetic. Thromb Res. 1988 Aug 15;51(4):417-23. PubMed PMID: 3187964.

9: Mazzone G, Arrigo-Reina R, Amico-Roxas M. [Research on monoamine oxidase inhibitors: synthesis of N-alkyl and N-aralkyl substituted ethylsyringoylhydrazides]. Farmaco Sci. 1976 Jul;31(7):517-26. Italian. PubMed PMID: 947782.