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132-32-1

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132-32-1 Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 132-32-1 differently. You can refer to the following data:
1. brown fine crystalline powder and chunks
2. 3-Amino-9-ethylcarbazole is a brown or tan, crystalline compound.

Uses

Different sources of media describe the Uses of 132-32-1 differently. You can refer to the following data:
1. 3-Amino-9-ethylcarbazole (AEC) has been used as a chromogen in immunohistochemistry to visualize the cells. It has also been used as a substrate in enzyme-linked immune absorbent spot (ELISpot).
2. 3-Amino-9-ethylcarbazole has been used to visualize the bound primary antibody by using a streptavidin method. It has also been used in visualizing tissue sections from tumour samples.

Definition

A hydrochloride salt and free amine solid compound.

General Description

Tan powder.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

3-Amino-9-ethylcarbazole neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. May generate hydrogen, a flammable gas, in combination with strong reducing agents such as hydrides.

Hazard

Questionable carcinogen; poison.

Health Hazard

ACUTE/CHRONIC HAZARDS: When heated to decomposition 3-Amino-9-ethylcarbazole emits toxic fumes.

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Some are oxidizers and may ignite combustibles (wood, paper, oil, clothing, etc.). Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated.

Safety Profile

Suspected carcinogen with experimental carcinogenic data. Poison by ingestion and intraperitoneal routes. When heated to decomposition it emits toxic fumes of NOx,.

Potential Exposure

Plant workers engaged in the manufacture of this compound and its use in pigment manufacture. Laboratory workers using this material in colorimetric enzyme assays and as a biological stain

Shipping

UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.

Incompatibilities

3-Amino-9-ethylcarbazole neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. May generate hydrogen, a flammable gas, in combination with strong reducing agents such as hydrides.

Waste Disposal

Incinerator equipped with a scrubber or thermal unit to reduce nitrogen oxides emissions.

Check Digit Verification of cas no

The CAS Registry Mumber 132-32-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 132-32:
(5*1)+(4*3)+(3*2)+(2*3)+(1*2)=31
31 % 10 = 1
So 132-32-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H14N2/c1-2-16-13-6-4-3-5-11(13)12-9-10(15)7-8-14(12)16/h3-9H,2,15H2,1H3

132-32-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (A2167)  3-Amino-9-ethylcarbazole [for Biochemical Research]  >90.0%(HPLC)(T)

  • 132-32-1

  • 1g

  • 260.00CNY

  • Detail
  • TCI America

  • (A2167)  3-Amino-9-ethylcarbazole [for Biochemical Research]  >90.0%(HPLC)(T)

  • 132-32-1

  • 5g

  • 750.00CNY

  • Detail
  • Alfa Aesar

  • (B22529)  3-Amino-9-ethylcarbazole, 95%   

  • 132-32-1

  • 25g

  • 513.0CNY

  • Detail
  • Alfa Aesar

  • (B22529)  3-Amino-9-ethylcarbazole, 95%   

  • 132-32-1

  • 100g

  • 1492.0CNY

  • Detail
  • Sigma-Aldrich

  • (06696)  3-Amino-9-ethylcarbazole  for HPLC derivatization, ≥97.0% (HPLC)

  • 132-32-1

  • 06696-1G

  • 236.34CNY

  • Detail
  • Sigma-Aldrich

  • (06696)  3-Amino-9-ethylcarbazole  for HPLC derivatization, ≥97.0% (HPLC)

  • 132-32-1

  • 06696-10G

  • 1,102.14CNY

  • Detail
  • Sigma-Aldrich

  • (06696)  3-Amino-9-ethylcarbazole  for HPLC derivatization, ≥97.0% (HPLC)

  • 132-32-1

  • 06696-10X1G

  • 2,048.67CNY

  • Detail

132-32-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Amino-9-ethylcarbazole

1.2 Other means of identification

Product number -
Other names 9-Ethylcarbazol-3-amine,AEC

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:132-32-1 SDS

132-32-1Related news

Structural dependences of the η 6 complexes of 3-Amino-9-ethylcarbazole (cas 132-32-1) with chromium tricarbonyl fragment on third-order optical nonlinearities09/30/2019

Degenerate four-wave mixing measurements, using the 35 ps pulses at 532 nm, have been employed to investigate the third-order nonlinear optical parameters of two chromium tricarbonyl complexes η 6-bonded to 3-amino-9-ethylcarbazole at either the NH2-substituted aryl ring (1) or the unsubstitute...detailed

Novel fluorescence sensor based on covalent immobilization of 3-Amino-9-ethylcarbazole (cas 132-32-1) via electrostatically assembled gold nanoparticle layer09/29/2019

A novel technique of immobilizing indicator dyes by electrostatic adsorption and covalent bonding to fabricate optical sensors was developed. 3-Amino-9-ethylcarbazole (AEC) was attached to the outmost surface of quartz glass slide via aminosilanizing the slide, crosslinking chitosan, adsorbing A...detailed

A novel fluorescence sensor based on covalent immobilization of 3-Amino-9-ethylcarbazole (cas 132-32-1) by using silver nanoparticles as bridges and carriers10/01/2019

A novel technique of covalent immobilization of indicator dyes in the preparation of fluorescence sensors is developed. Silver nanoparticles are used as bridges and carriers for anchoring indicator dyes. 3-amino-9-ethylcarbazole (AEC) was employed as an example of indicator dyes with terminal am...detailed

132-32-1Relevant articles and documents

A carbazole-based turn-on fluorescent probe for the detection of hydrazine in aqueous solution

Wang, Wei-Dong,Hu, Yang,Li, Qiao,Hu, Sheng-Li

, p. 206 - 211 (2018)

A carbazole-based fluorescent probe, 2-(9-ethyl-9H-carbazol-3-yl) isoindoline-1,3-dione, with a low detection limit (2.673 × 10?6 M) for the detection of hydrazine is designed and synthesized based on Gabriel reaction. The probe responds selectively to hydrazine over other amino compounds with marked fluorescence enhancement. Moreover, test paper experiments indicated its great potential in the environment monitoring of hydrazine in aqueous solution.

Introduction of a luminescent sensor for tracking trace levels of hydrazine in insect pollinated cropland flowers

Chattopadhyay, Ansuman,Das, Sujoy,Rissanen, Kari,Saha, Shrabani,Sahoo, Prithidipa,Sarkar, Olivia

supporting information, p. 17095 - 17100 (2021/10/04)

In recent years the excessive use of hydazine containing chemical pesticides and insecticides in farming practices is well pronounced, which directly or indirectly impart a great threat towards the total environment. Considering the above fact we are motivated to introduce a new, efficient and simple chemodosimeter (NCD) based on a carbazole-naphthalimide framework to recognize and estimate the mutagenic hydrazine within several affected cropland flowers. ProbeNCDcan detect hydrazine in a nanomolar range (65 nM or 2 ppb) in the presence of other metal ions, anions and amines, which gives it not only great potential but also makes it selective and sensitive. The sensing mechanism is confirmed by UV-vis, emission, and mass spectroscopy, and computational studies. We have successfully characterized probeNCDby1H and13C NMR and mass spectrometry as well as by single crystal analysis.

Use for RL intermediate condensation product synthesis process (by machine translation)

-

Paragraph 0017; 0018, (2017/08/29)

The present invention discloses a use for RL intermediate condensation product synthesis process, the process comprises the steps of: carbazole alkylation N - ethyl carbazole made, by nitration, reduction to generate a 3 - amino - N - ethyl carbazole, then in the organic solvent in the condensation reaction, use for intermediate condensate obtained RL; in this invention the condensation reaction using an alcohol as a solvent to replace the traditional O-chlorobenzene, improves the 3 - amino - N - ethyl carbazole conversion rate, and improves the use for RL crude purity and yield, and the process is stable, simple operation, high safety factor. (by machine translation)

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