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Tetrabutylphosphonium chloride

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96%

Sinônimo(s):

Tetra-n-butylphosphonium chloride

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About This Item

Fórmula linear:
(CH3CH2CH2CH2)4P(Cl)
Número CAS:
2304-30-5
Peso molecular:
294.88
Beilstein:
4019186
Número CE:
218-964-8
Número MDL:
MFCD00011854
Código UNSPSC:
12352001
ID de substância PubChem:
24848685
NACRES:
NA.22

Ensaio

96%

Formulário

liquid

características do produto alternativo mais ecológico

Catalysis
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sustainability

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62-66 °C (dec.) (lit.)

categoria alternativa mais ecológica

Aligned,

cadeia de caracteres SMILES

[Cl-].CCCC[P+](CCCC)(CCCC)CCCC

InChI

1S/C16H36P.ClH/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H/q+1;/p-1

chave InChI

IBWGNZVCJVLSHB-UHFFFAOYSA-M

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Descrição geral

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.

Aplicação


  • Insight into Cellulose Dissolution with the Tetrabutylphosphonium Chloride-Water Mixture using Molecular Dynamics Simulations.: This study investigates the molecular dynamics of cellulose dissolution in a Tetrabutylphosphonium chloride-water mixture, providing insights into its potential application in biomass processing and material science (Crawford and Ismail, 2020).

  • Thermodynamic and Transport Properties of Tetrabutylphosphonium Hydroxide and Tetrabutylphosphonium Chloride-Water Mixtures via Molecular Dynamics Simulation.: The research focuses on the thermodynamic and transport properties of Tetrabutylphosphonium chloride in water mixtures, highlighting its relevance in developing advanced ionic liquids for various industrial applications (Crawford and Ismail, 2020).

  • End-of-life Treatment of Poly(vinyl chloride) and Chlorinated Polyethylene by Dehydrochlorination in Ionic Liquids.: This article explores the use of Tetrabutylphosphonium chloride as an ionic liquid for the dehydrochlorination of PVC and CPE, demonstrating its utility in sustainable polymer recycling processes (Glas et al., 2014).

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 1 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1C - Skin Sens. 1B

Código de classe de armazenamento

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

>266.0 °F - closed cup

Ponto de fulgor (°C)

> 130 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificados de análise (COA)

Lot/Batch Number
MKCQ0277
MKCM3540
MKCM4645
MKCJ5911
MKCJ1433

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Wenbao Ma et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(30), 7287-7296 (2017-04-06)
The efficient and environmentally benign epoxidation of allylic alcohols has been attained by using new kinds of monomeric peroxotantalate anion-functionalized ionic liquids (ILs=[P
B J Dunn et al.
Toxicology, 24(3-4), 245-250 (1982-01-01)
Tetrabutyl phosphonium chloride and tetrabutyl phosphonium bromide were evaluated for their potential to cause primary dermal irritation and acute dermal toxicity in rabbits. Both chemicals were found to not only be severely irritating to skin, but the pure hygroscopic chemicals
Guohui Zhou et al.
The journal of physical chemistry. B, 111(25), 7078-7084 (2007-06-08)
An all-atom force field was set up for a new class of ionic liquids (ILs), tetrabutylphosphonium amino acid, on the basis of the AMBER force field with determining parameters related to the phosphorus atom and modifying several parameters. Ab initio
Mitsuru Abe et al.
Chemical communications (Cambridge, England), 48(12), 1808-1810 (2012-01-06)
Tetrabutylphosphonium hydroxide containing 40 wt% water dissolved 20 wt% cellulose at the final concentration within 5 minutes under mild stirring at 25 °C.
Shohei Saita et al.
Chemical communications (Cambridge, England), 49(1), 93-95 (2012-11-21)
The phase separation temperature of the tetrabutylphosphonium trifluoroacetate-water mixture, which undergoes a lower critical solution temperature-type phase transition, is highly sensitive to the hydrophilicity of added salts; this system can be used to compare the hydrophilicity of the added ions.
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