Welcome to LookChem.com Sign In|Join Free

CAS

  • or

22113-86-6

Post Buying Request

22113-86-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

22113-86-6 Usage

Conductivity

25.4 mS/cm

Check Digit Verification of cas no

The CAS Registry Mumber 22113-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,1 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22113-86:
(7*2)+(6*2)+(5*1)+(4*1)+(3*3)+(2*8)+(1*6)=66
66 % 10 = 6
So 22113-86-6 is a valid CAS Registry Number.
InChI:InChI=1/C2H7N.HNO3/c1-2-3;2-1(3)4/h2-3H2,1H3;(H,2,3,4)

22113-86-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethylammonium nitrate

1.2 Other means of identification

Product number -
Other names ethanamine,nitric acid

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:22113-86-6 SDS

22113-86-6Synthetic route

ethylamine
75-04-7

ethylamine

ethylammonium nitrate
22113-86-6

ethylammonium nitrate

Conditions
ConditionsYield
With nitric acid In water at 10℃; pH=7.3;100%
With nitric acid In water for 1h; pH=7.3; Cooling with ice;100%
With acide nitrique at 0℃;
ethylammonium nitrate
22113-86-6

ethylammonium nitrate

4-dimethylamino-benzaldehyde
100-10-7

4-dimethylamino-benzaldehyde

4-[(ethylimino)methyl]-N,N-dimethylbenzeneamine
59488-00-5

4-[(ethylimino)methyl]-N,N-dimethylbenzeneamine

Conditions
ConditionsYield
pH=6;97%
ethylammonium nitrate
22113-86-6

ethylammonium nitrate

anthranilic acid
118-92-3

anthranilic acid

orthoformic acid triethyl ester
122-51-0

orthoformic acid triethyl ester

3-ethyl-3H-quinazoline-4-one
3476-65-1

3-ethyl-3H-quinazoline-4-one

Conditions
ConditionsYield
at 45 - 46℃; for 0.416667h; Ionic liquid; Sonication; neat (no solvent);87%
ethylammonium nitrate
22113-86-6

ethylammonium nitrate

anthranilic acid amide
28144-70-9

anthranilic acid amide

orthoformic acid triethyl ester
122-51-0

orthoformic acid triethyl ester

A

4-Hydroxyquinazoline
491-36-1

4-Hydroxyquinazoline

B

3-ethyl-3H-quinazoline-4-one
3476-65-1

3-ethyl-3H-quinazoline-4-one

Conditions
ConditionsYield
at 45 - 46℃; for 0.333333h; Ionic liquid; Sonication; neat (no solvent);A 10%
B 86%
ethylammonium nitrate
22113-86-6

ethylammonium nitrate

4-hydroxy-benzaldehyde
123-08-0

4-hydroxy-benzaldehyde

4-[(ethylimino)methyl]phenol

4-[(ethylimino)methyl]phenol

Conditions
ConditionsYield
pH=6;64%
ethylammonium nitrate
22113-86-6

ethylammonium nitrate

benzaldehyde
100-52-7

benzaldehyde

N-(benzylidene)ethylamine
6852-54-6

N-(benzylidene)ethylamine

Conditions
ConditionsYield
14%
4-nitrobenzaldehdye
555-16-8

4-nitrobenzaldehdye

ethylammonium nitrate
22113-86-6

ethylammonium nitrate

N-(p-nitrobenzylidene)ethylamine
25105-58-2

N-(p-nitrobenzylidene)ethylamine

Conditions
ConditionsYield
10%
calcium cyanamide
156-62-7

calcium cyanamide

ethylammonium nitrate
22113-86-6

ethylammonium nitrate

ethyl guanidine
503-69-5

ethyl guanidine

Conditions
ConditionsYield
at 110℃;
ethylammonium nitrate
22113-86-6

ethylammonium nitrate

N-Cyanoguanidine
127099-85-8, 780722-26-1

N-Cyanoguanidine

ethyl guanidine
503-69-5

ethyl guanidine

Conditions
ConditionsYield
at 170℃;
ethylammonium nitrate
22113-86-6

ethylammonium nitrate

CH3CH2ND3(1+)*NO3(1-)=(CH3CH2ND3)NO3

CH3CH2ND3(1+)*NO3(1-)=(CH3CH2ND3)NO3

Conditions
ConditionsYield
With water-d2
ethylammonium nitrate
22113-86-6

ethylammonium nitrate

acetaldehyde
75-07-0

acetaldehyde

Conditions
ConditionsYield
With ammonium cerium(IV) nitrate; nitric acid In water at 54.9℃; Kinetics; Rate constant; other temperatures; ΔE(activ.), A, ΔH(excit.), ΔS(excit.), ΔG(excit.);
dinitrogen tetraoxide
10544-72-6

dinitrogen tetraoxide

ethylammonium nitrate
22113-86-6

ethylammonium nitrate

nitrosyl chloride

nitrosyl chloride

A

ethyl nitrite
109-95-5

ethyl nitrite

B

ethanol
64-17-5

ethanol

water-d2
7789-20-0

water-d2

ethylammonium nitrate
22113-86-6

ethylammonium nitrate

CH3CH2ND3(1+)*NO3(1-)=(CH3CH2ND3)NO3

CH3CH2ND3(1+)*NO3(1-)=(CH3CH2ND3)NO3

Conditions
ConditionsYield
In water-d2 concn. (vacuum, room temp., 24 h), drying (over molecular sieves, 3 d);
piperidine
110-89-4

piperidine

ethylammonium nitrate
22113-86-6

ethylammonium nitrate

2,4-Dinitrofluorobenzene
70-34-8

2,4-Dinitrofluorobenzene

A

2,4-dinitro-N-ethylaniline
3846-50-2

2,4-dinitro-N-ethylaniline

B

1-(2,4-dinitrophenyl)piperidine
839-93-0

1-(2,4-dinitrophenyl)piperidine

Conditions
ConditionsYield
In acetonitrile at 25℃; Kinetics; Equilibrium constant; Concentration;
ethylammonium nitrate
22113-86-6

ethylammonium nitrate

2,4-Dinitrofluorobenzene
70-34-8

2,4-Dinitrofluorobenzene

N-butylamine
109-73-9

N-butylamine

A

2,4-dinitro-N-butylaniline
13059-86-4

2,4-dinitro-N-butylaniline

B

2,4-dinitro-N-ethylaniline
3846-50-2

2,4-dinitro-N-ethylaniline

Conditions
ConditionsYield
In acetonitrile at 25℃; Kinetics; Equilibrium constant; Concentration;
ethylammonium nitrate
22113-86-6

ethylammonium nitrate

anthranilic acid amide
28144-70-9

anthranilic acid amide

orthoformic acid triethyl ester
122-51-0

orthoformic acid triethyl ester

aniline
62-53-3

aniline

A

3-phenyl-4(3H)-quinazolinone
16347-60-7

3-phenyl-4(3H)-quinazolinone

B

4-Hydroxyquinazoline
491-36-1

4-Hydroxyquinazoline

C

3-ethyl-3H-quinazoline-4-one
3476-65-1

3-ethyl-3H-quinazoline-4-one

Conditions
ConditionsYield
at 45 - 46℃; Ionic liquid; Sonication; neat (no solvent);A 4.1 %Chromat.
B 12.1 %Chromat.
C 46.7 %Chromat.
BrCeCl3(1-)*C21H38N(1+)

BrCeCl3(1-)*C21H38N(1+)

ethylammonium nitrate
22113-86-6

ethylammonium nitrate

cerium(IV) oxide

cerium(IV) oxide

Conditions
ConditionsYield
at 400℃; for 1h; Temperature;

22113-86-6Upstream product

22113-86-6Relevant articles and documents

Structure-energy relations in hen egg white lysozyme observed during refolding from a quenched unfolded state

Cho, Theresa Y.,Byrne, Nolene,Moore, David J.,Pethica, Brian A.,Austen Angell,Debenedetti, Pablo G.

, p. 4441 - 4443 (2009)

We use infrared spectroscopy to study the evolution of protein folding intermediate structures on arbitrarily slow time scales by rapidly quenching thermally unfolded hen egg white lysozyme in a glassy matrix, followed by reheating of the protein to refold; upon comparison with differential scanning calorimetric experiments, low-temperature structural changes that precede the formation of energetic native contacts are revealed. The Royal Society of Chemistry 2009.

Volumetric properties of ethylammonium nitrate + γ-butyrolactone binary systems: Solvation phenomena from density and raman spectroscopy

Zarrougui, Ramzi,Dhahbi, Mahmoud,Lemordant, Daniel

, p. 1531 - 1548 (2010)

The densities of binary mixtures of ethylammonium nitrate (EAN) ionic liquid (IL) and γ-butyrolactone (BL) have been measured over the entire range of concentrations at 293.15, 298.15, 303.15, 308.15, 313.15 and 318.15 K and under ambient pressure. Experimental densities were used to calculate excess molar volumes VmE, isobaric and excess isobaric expansion coefficients α and α E. The excess molar volumes have both negative and positive values, while the excess isobaric expansion coefficients are negative over the entire composition range. The V mE values have been fitted to the Redlich-Kister polynomial equation, and other volumetric properties such as the partial molar volumes V mi, the excess partial molar volume Vmi E and the partial molar volumes at infinite dilution V miE were calculated. The results have been interpreted in terms of dipole-dipole interactions, hydrogen bonds formation and structural factors of these mixtures. The FT-Raman spectroscopy study of the intensity variations of some characteristic bands such as the C=O stretching band at 1763 cm-1, C-O symmetric stretching band at 932 cm-1 and C-C stretching band at 872 cm-1 of BL has been undertaken. The solvation phenomenon is evidenced by the modifications of these band intensities due to the presence of the IL ions. Moreover, the Raman spectroscopy corroborates the volumetric study. The average number of BL molecules in the primary solvation shell of the ethylammonium cation lies between 3 and 4 depending on the temperature.

Measurements and correlation of viscosity and conductivity for the mixtures of ethylammonium nitrate with organic solvents

Litaeim, Yousra,Dhahbi, Mahmoud

, p. 42 - 50 (2010)

Transport physicochemical properties of binary mixtures ionic liquid/organic solvent (IL/OS) were studied. Systematical measurements of viscosities (η) and conductivities (Λ) for the binary mixtures of ethylammonium nitrate (EAN) with different OS, over the whole composition range and at temperature ranging from 273.15 K to 313.15 K, were performed. The variation tendency of viscosities/conductivities with composition of the mixtures was explained through the disruption of molecular solutes to ionic association or aggregation of the ionic liquids and correlation between them is carried out by means of Walden product (W). A semi-empirical equation proposed by Jones and Dole was used to describe the variation of viscosity with salt concentration (C). At low concentration of EAN, molar conductivity follows cube root law predicted by the quasi-lattice model. The two transport processes are well described by Arrhenius type laws from which the activation energies for the viscosity (Ea,η) and conductivity (Ea,Λ) are deduced.

Anhydrous proton exchange membranes at elevated temperatures: Effect of protic ionic liquids and crosslinker on proton conductivity

Yang, Yi,Gao, Hejun,Zheng, Liqiang

, p. 17683 - 17689 (2015)

A series of novel anhydrous proton exchange membranes (poly(vinyl alcohol)-citric acid-ionic liquid (PVA-CA-IL)) were prepared using the low cost ionic liquids ethylammonium nitrate (EAN), diethylammonium nitrate (DEAN), and triethylammonium nitrate (TEAN) as conductive fillers in PVA support membrane. The properties of the PVA-CA-IL membranes can be controlled by changing the molar ratio of the PVA, ILs and CA. The thermal stability of PVA-CA-IL membrane was measured by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC), and the microstructure was investigated using scanning electron microscopy (SEM) and the Anton-paar SAX Sess mc2 system (SAXS). The effects of temperature, ILs and crosslinker dosage on proton conductivity were also systematically investigated. The results showed that the PVA-CA-IL membranes had excellent performance. The proton conductivity of PVA-CA-EAN (mole ratio = 1:0.05:0.4) could reach up to 7.8 mS cm-1 at 140 °C. The introduction of ionic liquid into PVA membrane constituted a new and efficient kind of anhydrous proton exchange membrane. This journal is

First fluorinated zwitterionic micelle with unusually slow exchange in an ionic liquid

Wang, Xiaolin,Long, Panfeng,Dong, Shuli,Hao, Jingcheng

, p. 14380 - 14385 (2013)

The micellization of a fluorinated zwitterionic surfactant in ethylammonium nitrate (EAN) was investigated. The freeze-fracture transmission electron microscope (FF-TEM) observations confirm the formation of spherical micelles with the average diameter 25.45 ± 3.74 nm. The micellization is an entropy-driven process at low temperature but an enthalpy-driven process at high temperature. Two sets of 19F NMR signals above the critical micelle concentration (cmc) indicate that the unusually slow exchange between micelles and monomers exists in ionic liquid; meanwhile, surfactant molecules are more inclined to stay in micelle states instead of monomer states at higher concentration. Through the analysis of the half line width (Δν 1/2), we can obtain the kinetic information of fluorinated zwitterionic micellization in an ionic liquid.

Cytotoxicity of protic ionic liquids towards the HaCat cell line derived from human skin

Abraham, Amanda N.,Arunkumar, Radhika,Drummond, Calum J.,Greaves, Tamar L.,Shukla, Ravi

, (2020/07/03)

In this work we have investigated the toxicity of 10 PILs, consisting of ethyl-, ethanol-, diethanol- and triethanolammonium cations paired with nitrate, formate, acetate and glycolate anions. Their toxicity was quantified by the EC50 values of each of these PILs towards HaCat cells, which are derived from human skin cells. Additional salts and solvents were used for comparison including DMSO, choline chloride, potassium nitrate, sodium acetate and ethanol to distinguish if the toxicity changes were due to ionicity, short chain amphiphilic behaviour, or specific ion effects. The toxicity followed the general trend of choline chloride acetate containing PILs DMSO sodium acetate ethanol nitrate containing PILs or salt. Ethanolammonium acetate and ethylammonium acetate were identified as having the lowest toxicities of the PILs, being slightly more toxic than choline chloride or DMSO. Overall the toxicity was found to be highly dependent on the cation and anion combination, with the anion having a stronger affect. It was evident that the PILs can be tailored to vary their toxicities, and this is expected to be dependent on which cell lines are used.

Protic ionic liquids as catalysts for a three-component coupling/hydroarylation/dehydrogenation tandem reaction

Muntzeck, Maren,Wilhelm, René

, p. 515 - 519 (2018/06/18)

Protic ionic liquids with nitrate anions were used as solvents and catalysts for a three-component oxidative dehydrogenation tandem reaction via the coupling and hydroarylation of benzaldehyde, aniline, and phenylacetylene to a quinoline derivative. The reaction was supported by air and microwave irradiation. The presence of nitrate as counter anion in the protic ionic liquids was essential for the reaction.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 22113-86-6