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58464-25-8

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58464-25-8 Usage

General Description

1,2,3,3-Tetramethylbenz[e]indolium iodide is a chemical compound with the molecular formula C17H18IN. It is a dark red crystalline solid that is commonly used in organic chemistry as a catalyst and in the synthesis of various organic compounds. It is also known for its ability to function as a fluorescent probe for the detection of proteins and nucleic acids in biological samples. 1,2,3,3-Tetramethylbenz[e]indolium iodide is a versatile compound with a wide range of applications in chemical and biological research.

Check Digit Verification of cas no

The CAS Registry Mumber 58464-25-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,6 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58464-25:
(7*5)+(6*8)+(5*4)+(4*6)+(3*4)+(2*2)+(1*5)=148
148 % 10 = 8
So 58464-25-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H18N/c1-11-16(2,3)15-13-8-6-5-7-12(13)9-10-14(15)17(11)4/h5-10H,1-4H3/q+1

58464-25-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,3-tetramethylbenzo[e]indol-3-ium

1.2 Other means of identification

Product number -
Other names 1,1,2,3-tetramethyl-1H-benz[e]indol-3-ium iodide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58464-25-8 SDS

58464-25-8Relevant articles and documents

Viscosity sensitive semisquaraines based on 1, 1, 2-trimethyl-1H-benzo[e]indole: Photophysical properties, intramolecular charge transfer, solvatochromism, electrochemical and DFT study

Khopkar, Sushil,Jachak, Mahesh,Shankarling, Ganapati

, p. 123 - 135 (2019)

1, 1, 2-Trimethyl-1H-benzo[e]indole based D-π-A type semisquaraines denoted as, SSK 1–3 were synthesized to investigate their primary photophysical properties, intramolecular charge transfer, solvatochromism, electrochemical properties and viscosity dependent enhanced emission. These semisquaraines contain 1, 1, 2-trimethyl-1H-benzo[e]indole and squaryl ring as donor and acceptor respectively. These dyes displayed absorption between 437 and 444 nm and emission in the range of 469–493 nm. Stokes shift of the synthesized compounds were in the range of 32–54 nm. The SSK 1–3 exhibited intense yellow-orange colored solid state fluorescence (Fmax = 520–549 nm). These dyes exhibited intramolecular charge transfer characteristics which were confirmed from their oscillator strengths, transition dipole moments, ground and excited state dipole moments and generalized Mulliken-Hash analysis (GMH). Moreover, the positive emission solvatochromic behaviour (Δλem = 21–24 nm) of these dyes was quantitatively analyzed from different solvent polarity plots. More interestingly, these D-π-A type FMRs displayed viscosity sensitive emission enhancement (23 to 32 fold increase in fluorescence intensity) in 99% methanol:glycerol system at the visible region of electromagnetic spectrum (450–650 nm). The molecular structures of SSK 1–3 were correlated with photophysical properties using density functional theory (DFT) and theoretical absorption spectra in eight different solvents were obtained from time dependent density functional theory (TD-DFT).

A novel off-on fluorescent probe for sensitive imaging of mitochondria-specific nitroreductase activity in living tumor cells

Huang, Bo,Chen, Wen,Kuang, Yong-Qing,Liu, Wei,Liu, Xian-Jun,Tang, Li-Juan,Jiang, Jian-Hui

, p. 4383 - 4389 (2017)

Sensitive and selective detection and imaging of nitroreductase (NTR) in cancer cells is of great importance for better understanding their biological functions. Since there are a few fluorescent probes concerning NTR activity specifically located in mito

Large-sized benzo[: E] indolium salt single crystals with high optical nonlinearity

Shang, Shufang,Li, Ruian,Ping, Linjun,Luo, Wenzhen,Hai, Mingtan,Yang, Zhou,Wang, Dong,Cao, Hui,He, Wanli

, p. 5626 - 5632 (2019)

In this paper, a series of D-π-A type benzo[e]indolium salts with highly efficient nonlinear optical performance has been synthesized. Out of the three new benzo[e]indolium salts, (E)-2-(2-hydroxy-3-methoxystyryl)-1,1,3-trimethyl-1H-benzo[e]indol-3-ium iodide (HMTB-1) and (E)-2-(2-hydroxy-4-methoxystyryl)-1,1,3-trimethyl-1H-benzo[e]indol-3-ium iodide (HMTB-2) possess SHG properties, and their maximum powder second harmonic generation (SHG) efficiency is around 0.6 times that of DAST (4-N,N-dimethylamino-4′-N′-methyl-stilbazolium tosylate) at a non-resonant wavelength of λ = 1570 nm. Single crystals of the two noncentrosymmetric salts were successfully grown by using a slow cooling method, and we were able to obtain very large bulk single crystals, about 17 mm × 9 mm × 3 mm, of HMTB-2. X-ray crystallographic analysis indicated that both of the new salts belong to the monoclinic space group Cc (point group m, Z = 4). HMTB-1 forms a noncentrosymmetric phase with methanol through hydrogen bonding.

FRET-based ratiometric fluorescent detection of arginine in mitochondrion with a hybrid nanoprobe

Li, Yueyue,Ban, Yanan,Wang, Ruihui,Wang, Zheng,Li, Zhanxian,Fang, Chenjie,Yu, Mingming

, p. 443 - 446 (2020)

A ratiometric fluorescent hybrid nanoprobe CDs-1 for arginine (Arg), exhibiting high sensitivity (the limit of detection, LOD, being 6.5 × 10?8 mol/L) and excellent selectivity and anti-interference ability, was fabricated through fluorescence resonance energy transfer (FRET) and the electrostatic attraction between positively-charged hemicyanine molecules and negatively-charged carbon dots (CDs). Arg can be quantitatively detected in the concentration range from 6.0 × 10?5 mol/L to 2.7 × 10?4 mol/L. Further, due to its ability to target mitochondrion and low cytotoxicity, intracellular Arg was successfully tracked through ratiometric fluorescence imaging.

Bioorthogonal Ligation-Activated Fluorogenic FRET Dyads

Albitz, Evelin,Kern, Dóra,Kormos, Attila,Bojtár, Márton,T?r?k, Gy?rgy,Biró, Adrienn,Szatmári, ágnes,Németh, Krisztina,Kele, Péter

supporting information, (2021/12/30)

An energy transfer-based signal amplification relay concept enabling transmission of bioorthogonally activatable fluorogenicity of blue-excitable coumarins to yellow/red emitting cyanine frames is presented. Such relay mechanism resulted in improved cyani

Active inorganic sulfur species two-photon fluorescent probe as well as synthesis method and application thereof

-

Paragraph 0051-0052; 0055, (2021/03/24)

The invention relates to an active inorganic sulfur species two-photon fluorescent probe, which takes 1-pyrenecarboxaldehyde-hemicyanine as a parent and has a structural general formula shown in the specification. The active inorganic sulfur species two-p

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