Skip to Content
Merck
All Photos(1)

Key Documents

T76805

Sigma-Aldrich

2,3,3-Trimethylindolenine

98%

Synonym(s):

2,3,3-Trimethyl-3H-indole

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C11H13N
CAS Number:
Molecular Weight:
159.23
Beilstein:
119740
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

refractive index

n20/D 1.549 (lit.)

bp

228-229 °C/744 mmHg (lit.)

density

0.992 g/mL at 25 °C (lit.)

SMILES string

CC1=Nc2ccccc2C1(C)C

InChI

1S/C11H13N/c1-8-11(2,3)9-6-4-5-7-10(9)12-8/h4-7H,1-3H3

InChI key

FLHJIAFUWHPJRT-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

2,3,3-Trimethylindolenine is an indolenine compound used as a reactant in organic synthesis reactions.

Application

  • Squarylium-based chromogenic anion sensors.: This research explores the synthesis and application of squarylium-based sensors, which includes 2,3,3-Trimethylindolenine as a crucial component. The study focuses on the effectiveness of these sensors in detecting various anions through chromogenic changes, highlighting the compound′s role in developing advanced chemical sensing technologies (Lee EM et al., 2012).

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

199.4 °F - closed cup

Flash Point(C)

93 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Chanuk Jeong et al.
Journal of controlled release : official journal of the Controlled Release Society, 329, 50-62 (2020-12-02)
Near-infrared (NIR)-induced dye-based theranostic drug delivery carriers are used for critical image-guided chemo-photothermal cancer therapy. However, most carriers fail to deliver sufficient heat and fluorescence efficiently due to direct π-π stacking of the aromatic rings of the NIR dye and
Juewei Ning et al.
Molecular medicine reports, 15(6), 3761-3766 (2017-04-26)
The future of personalized cancer treatments relies on the development of functional agents that have tumor-targeted anticancer activities and can be detected in tumors using imaging. However, application of these functional agents in the clinic has been limited due to
Hang Zhang et al.
Nature communications, 10(1), 3267-3267 (2019-07-25)
Living systems have inspired research on non-biological dynamic materials and systems chemistry to mimic specific complex biological functions. Upon pursuing ever more complex life-inspired non-biological systems, mimicking even the most elementary aspects of learning is a grand challenge. We demonstrate
Antonio Setaro et al.
Nature communications, 8, 14281-14281 (2017-01-31)
Covalent functionalization tailors carbon nanotubes for a wide range of applications in varying environments. Its strength and stability of attachment come at the price of degrading the carbon nanotubes sp
Ilkoo Noh et al.
Advanced science (Weinheim, Baden-Wurttemberg, Germany), 5(3), 1700481-1700481 (2018-03-30)
A noninvasive and selective therapy, photodynamic therapy (PDT) is widely researched in clinical fields; however, the lower efficiency of PDT can induce unexpected side effects. Mitochondria are extensively researched as target sites to maximize PDT effects because they play crucial

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service