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1,5-Pentaneethonium Dibromide is a divalent quaternary amine compound that has been utilized in the study of various zeolites, focusing on their synthesis and interactions with cavities and channels within the zeolite structures.

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  • 7128-82-7 Structure
  • Basic information

    1. Product Name: 1,5-PENTANEETHONIUM DIBROMIDE
    2. Synonyms: 1,5-Pentanediaminium, N,N,N,N',N',N'-hexaethyl-, dibromide;1,5-pentanediaminium,N,N,N,N’,N’,N’-hexaethyl-,dibromide;Ammonium, pentamethylenebis(triethyl-, dibromide;N,N,N,N’,N’,N’-hexaethyl-1,5-pentanediaminiumdibromide;pentamethylenebis(triethyl-ammoniudibromide;pentamethylenebis(triethylammoniumbromide);pentamethylenebis[triethylammoniumbromide];1,5-PENTANEETHONIUM DIBROMIDE
    3. CAS NO:7128-82-7
    4. Molecular Formula: 2Br*C17H40N2
    5. Molecular Weight: 432.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 7128-82-7.mol
  • Chemical Properties

    1. Melting Point: 276-278 °C (decomp)
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,5-PENTANEETHONIUM DIBROMIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,5-PENTANEETHONIUM DIBROMIDE(7128-82-7)
    11. EPA Substance Registry System: 1,5-PENTANEETHONIUM DIBROMIDE(7128-82-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 7128-82-7(Hazardous Substances Data)

7128-82-7 Usage

Uses

Used in Zeolite Research:
1,5-Pentaneethonium Dibromide is used as a guest molecule for studying the synthesis and cavity/channel interactions of zeolites. Its application in this field aids in understanding the properties and behavior of zeolites, which are important materials in various industrial applications, such as catalysis and gas separation.

Check Digit Verification of cas no

The CAS Registry Mumber 7128-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,2 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7128-82:
(6*7)+(5*1)+(4*2)+(3*8)+(2*8)+(1*2)=97
97 % 10 = 7
So 7128-82-7 is a valid CAS Registry Number.

7128-82-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Ammonium, pentamethylenebis(triethyl-, dibromide

1.2 Other means of identification

Product number -
Other names pentamethylenebis(triethyl-ammoniudibromide

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:7128-82-7 SDS

7128-82-7Synthetic route

1,5-dibromo-pentane
111-24-0

1,5-dibromo-pentane

triethylamine
121-44-8

triethylamine

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide
7128-82-7

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide

Conditions
ConditionsYield
In acetone for 24h; Reflux;90%
In neat (no solvent) at 110℃; for 24h; Autoclave;64%
With ethanol
In methanol at 65℃; for 72h;
(5-bromopentyl)triethylammonium bromide
104304-09-8

(5-bromopentyl)triethylammonium bromide

triethylamine
121-44-8

triethylamine

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide
7128-82-7

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide

Conditions
ConditionsYield
In propan-1-ol Heating;72%
1,5-dibromo-pentane
111-24-0

1,5-dibromo-pentane

Wang resin-OC(O)CH2N=CPh2

Wang resin-OC(O)CH2N=CPh2

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide
7128-82-7

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 21 percent / hexane / 10 h / Heating
2: 72 percent / propan-1-ol / Heating
View Scheme
triethylamine
121-44-8

triethylamine

DL-methionine nitrile

DL-methionine nitrile

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide
7128-82-7

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 21 percent / hexane / 10 h / Heating
2: 72 percent / propan-1-ol / Heating
View Scheme
1,5-dibromo-pentane
111-24-0

1,5-dibromo-pentane

ethanol
64-17-5

ethanol

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide
7128-82-7

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide

Conditions
ConditionsYield
With triethylamine Heating / reflux;
aluminum(III) nitrate nonahydrate

aluminum(III) nitrate nonahydrate

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide
7128-82-7

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide

sodium hydroxide
1310-73-2

sodium hydroxide

P1 zeolite

P1 zeolite

Conditions
ConditionsYield
With silica gel In water colloidal silica and Et3N(CH2)5NEt3Br2 added to aq. soln. of Al(NO3)3*9H2O and NaOH; stirred (room temp., 1 day); heated (160°C, 8 days,autoclave, rotation 60 rpm); filtered off; washed repeatedly (water); dried overnight (room temp.); elem. anal.; thermal anal.;
aluminum(III) nitrate nonahydrate

aluminum(III) nitrate nonahydrate

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide
7128-82-7

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide

potassium hydroxide

potassium hydroxide

SUZ-4 zeolite

SUZ-4 zeolite

Conditions
ConditionsYield
With silica gel In water colloidal silica and Et3N(CH2)5NEt3Br2 added to aq. soln. of Al(NO3)3*9H2O and KOH; stirred (room temp., 1 day); heated (160°C, 8 days, autoclave, rotation 60 rpm); filtered off; washed repeatedly (water); dried overnight (room temp.); elem. anal.; thermal anal.;
N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide
7128-82-7

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide

C17H40N2(2+)*2HO(1-)

C17H40N2(2+)*2HO(1-)

Conditions
ConditionsYield
With anion exchange resin DIAION
N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide
7128-82-7

N1,N1,N1,N5,N5,N5-hexaethylpentane-1,5-diamonium dibromide

C17H40N2(2+)*2F6P(1-)

C17H40N2(2+)*2F6P(1-)

Conditions
ConditionsYield
With ammonium hexafluorophosphate In water for 4h;

7128-82-7Downstream Products

7128-82-7Relevant articles and documents

The use of a diammonium salt in the synthesis of organic carbonates from epoxides and CO2: promoting effect of support

Arzumanyan, A. V.,Chowdhury, B.,Davankov, V. A.,Lyubimov, S. E.,Muzafarov, A. M.,Zvinchuk, A. A.

, p. 1076 - 1079 (2020)

Onium salt, N1, N1, N1, N5, N5, N5-hexaethylpentane-1,5-diammonium dibromide, was used as a catalyst for the addition of CO2 to epoxides. An influence of insoluble supports on the rate of the process as well as possibility of recycling of the catalytic system are described. In addition, the effects of temperature and CO2 pressure on the yields of products are discussed.

Binuclear pyridine acid ionic liquid, and preparation method and application thereof

-

Paragraph 0042; 0044-0046, (2021/08/21)

The invention discloses a binuclear pyridine acid ionic liquid, and a preparation method and application thereof. The chemical formula of the ionic liquid is Cn [N222] 2 [Py] 2, triethylamine, dibromo alkane and 3, 6-clopyralid are used as raw materials, the binuclear pyridine acid weeding ionic liquid is obtained through an alkanization reaction, a double decomposition reaction and a neutralization reaction, and the prepared binuclear pyridine acid ionic liquid has the characteristics of being medium in water solubility, not prone to volatilization and migration, high in biological activity and the like, and when acting on herbicides in pesticide chemistry, the binuclear pyridine acid ionic liquid has efficient herbicide physicochemical properties, high herbicidal activity and low crop toxicity.

Dinuclear quaternary ammonium salt ionic liquid compound as well as preparation method and application thereof

-

Paragraph 0054-0055, (2021/09/01)

The present invention discloses a double-core quaternary ammonium salt ionic liquid compound having two quaternary ammonium root cations and selected from the group consisting of formate. The acetate, propionate, butyrate, acetate radical anion. The invention further discloses a preparation method and of the ionic liquid, H and thereof. 2 The application of S absorption removal. The ionic liquid is novel in structure, convenient to synthesize and capable of effectively avoiding the defects of large pollution, strong corrosion, high energy consumption and the like of a traditional organic amine process. In addition, the ionic liquid H according to the present invention is used with respect to a normal ionic liquid. 2 S Absorbs capacity higher, and the effect is showing.

Imine macrocycle with a deep cavity: Guest-selected formation of syn/anti configuration and guest-controlled reconfiguration

He, Zhenfeng,Ye, Gang,Jiang, Wei

supporting information, p. 3005 - 3012 (2015/02/05)

A dynamic covalent bond is one of the ideal linkages for the construction of large and robust organic architectures. In the present article, we show how organic templates can efficiently transform a complex dynamic imine library into a dynamic imine macrocycle. Not only is the constitution well controlled, but also the syn/anti host configuration is efficiently selected and even the orientation of the guest in the asymmetric cavity of the host can be well aligned. This is attributed to the delicate balance and the cooperation of multiple noncovalent interactions between the hosts and the guests. Through sequential additions of three guests in appropriate amounts, controlled structural reconfiguration of dynamic covalent architectures has been achieved for the first time.

Designing the synthesis of catalytically active Ti-β by using various new templates in the presence of fluoride anion

Sasidharan, Manickam,Bhaumik, Asim

experimental part, p. 16282 - 16294 (2012/01/14)

Crystallization of large-pore Ti-β by using a variety of diquaternary ammonium derivatives of dibromoalkane and amines such as triethylamine, 1,4-diazabicyclo[2,2,2]octane (DABCO), and quinuclidine as structure-directing agents (SDA) is described. The size of hydrophobic bridging alkyl-chain length of the template [R3N+-(CH2)x-N +R3](OH-)2 directs the final crystalline product: Ti-β, Ti-ZSM-12, Ti-nonasil or Ti-ZSM-5, as x gradually changes from 6 to 1, in the fluoride medium under hydrothermal conditions. A dense phase such as Ti-nonasil (clathrasil type) is crystallized as the size of hydrophobic bridging alkyl-chain length decreases. The use of F- anions as a mineralizer and Ti4+ as a heteroatom in the synthesis gel also influences the selectivity of final crystalline product. The phase purity and incorporation of Ti4+ into the lattice of β (BEA) and ZSM-12 frameworks are confirmed using XRD, UV-visible, FT-IR, 29Si NMR spectroscopes, elemental analysis (ICP), surface area measurements and catalytic test reactions. The morphology of Ti-β samples is dependent on the nature of the structure-directing agent as revealed by the scanning electron microscopic (SEM) observations. The catalytic activity in the epoxidation of 4-vinyl-1-cyclohexene is increased with the amount of tetrahedral Ti4+ atoms in the framework. The new templates can be effectively used for preparation of catalytically active Ti-β with the minimum number of framework defect sites.

Process for manufacturing molecular sieve of MFS framework type and its use

-

Page/Page column 6, (2008/06/13)

A method of making a crystalline molecular sieve of MFS framework type, said method comprising the steps of (a) adding at least one source of ions of tetravalent element (Y), at least one source of ions of trivalent element (X), at least one hydroxide source (OH?), at least one structure-directing-agent (R), at least one seed source (Seed), and water (H2O) to form a mixture having the following mole composition (expressed in term of oxide): [in-line-formulae]YO2:(n)X2O3:(x)OH?:(y)R:(z)H2O+(m)Seed[/in-line-formulae] wherein the m is in the range of from about 10 wtppm to about 2 wt. % (based on total weight of the synthesis mixture), the n is in the range of from about 0.005 to 0.05, the x is in the range of from about 0.01 to about 0.3, the y is in the range of from about 0.03 to about 2; and the z is in the range of from about 3 to about 30; and (b) treating said mixture under crystallization conditions to form said crystalline molecular sieve substantially free of non-MFS material, wherein said crystallization conditions comprise a temperature in the range of from about 150° C. to about 250° C., and crystallization time less than 100 hr, the weight hourly throughput is at least 0.001 hr?1.

Ion channel topography of the neuronal nicotinic acetylcholine receptor: Pharmacochemical approaches

Gmiro,Brovtsyna,Serdyuk,Lukomskaya

, p. 116 - 127 (2007/10/03)

Forty-three bisammonium ganglionic blockers were synthesized to study the structure of the ion channel of nicotinic acetylcholine receptor. The conformational parameters of these blockers were studied, and their effects toward the ganglionic transmission in situ on the sympathetic feline superior cervical ganglia and in vitro on the parasympathetic guinea-pig small intestine ganglia were determined. A model of the binding site for the bisammonium ganglionic blockers in the neuronal ion channel was proposed.

The Quarternisation of Tertiary Amines with Dihalomethane

Almarzoqi, B.,George, A. V.,Isaacs, N. S.

, p. 601 - 608 (2007/10/02)

Whereas dichloromethane is inert towards reaction with most tertiary amines under atmospheric conditions, it readily reacts with a wide variety at high pressures to produce α-chloro quaternary ammonium and even bis-ammonium salts.The reaction of dichloromethane and dibromomethane with eleven tertiary amines and properties of the products are described.

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