์ฝ˜ํ…์ธ ๋กœ ๊ฑด๋„ˆ๋›ฐ๊ธฐ
Merck
๋ชจ๋“  ์‚ฌ์ง„(1)

์ฃผ์š” ๋ฌธ์„œ

241970

Sigma-Aldrich

Tetrapentylammonium bromide

≥99%

๋™์˜์–ด(๋“ค):

Tetra-n-pentylammonium bromide

๋กœ๊ทธ์ธ์กฐ์ง ๋ฐ ๊ณ„์•ฝ ๊ฐ€๊ฒฉ ๋ณด๊ธฐ


About This Item

Linear Formula:
[CH3(CH2)4]4N(Br)
CAS Number:
Molecular Weight:
378.47
Beilstein:
3658171
EC Number:
MDL number:
UNSPSC ์ฝ”๋“œ:
12352116
PubChem Substance ID:
NACRES:
NA.22

Quality Level

๋ถ„์„

≥99%

mp

100-101 ยฐC (lit.)

SMILES string

[Br-].CCCCC[N+](CCCCC)(CCCCC)CCCCC

InChI

1S/C20H44N.BrH/c1-5-9-13-17-21(18-14-10-6-2,19-15-11-7-3)20-16-12-8-4;/h5-20H2,1-4H3;1H/q+1;/p-1

InChI key

SPALIFXDWQTXKS-UHFFFAOYSA-M

์œ ์‚ฌํ•œ ์ œํ’ˆ์„ ์ฐพ์œผ์‹ญ๋‹ˆ๊นŒ? ๋ฐฉ๋ฌธ ์ œํ’ˆ ๋น„๊ต ์•ˆ๋‚ด

๊ด€๋ จ ์นดํ…Œ๊ณ ๋ฆฌ

์ผ๋ฐ˜ ์„ค๋ช…

Tetrapentylammonium bromide is a quaternary ammonium salt with pentyl chains and a bromide counterion, which is generally used as a phase transfer catalyst.

์• ํ”Œ๋ฆฌ์ผ€์ด์…˜

Tetrapentylammonium bromide can be used:
  • As a versatile structure-directing agent for the synthesis of Zeolite-like heterobimetallic cyanide frameworks.
  • As an alkylating agent for rhodium(I)-catalyzed alkylation reaction of benzylic amines and for N-alkylation of azaheterocycles.
  • As a precursor to prepare a Cobalt-complex, {[(Pentyl)4N]3CoBr3}Cl2, which is used as a catalyst in the synthesis of multiwalled carbon nanotubes (MWCNTs).


Electrochemical synthesis of stable graphite intercalation compounds (GICs) containing tetrapentylammonium cations has been reported.

ํ”ฝํ† ๊ทธ๋žจ

Exclamation mark

์‹ ํ˜ธ์–ด

Warning

์œ ํ•ด ๋ฐ ์œ„ํ—˜ ์„ฑ๋ช…์„œ

์˜ˆ๋ฐฉ์กฐ์น˜ ์„ฑ๋ช…์„œ

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

ํ‘œ์  ๊ธฐ๊ด€

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (ยฐF)

Not applicable

Flash Point (ยฐC)

Not applicable

๊ฐœ์ธ ๋ณดํ˜ธ ์žฅ๋น„

dust mask type N95 (US), Eyeshields, Gloves


๊ฐ€์žฅ ์ตœ์‹  ๋ฒ„์ „ ์ค‘ ํ•˜๋‚˜๋ฅผ ์„ ํƒํ•˜์„ธ์š”:

์‹œํ—˜ ์„ฑ์ ์„œ(COA)

Lot/Batch Number

์ ํ•ฉํ•œ ๋ฒ„์ „์„ ์ฐพ์„ ์ˆ˜ ์—†์œผ์‹ ๊ฐ€์š”?

ํŠน์ • ๋ฒ„์ „์ด ํ•„์š”ํ•œ ๊ฒฝ์šฐ ๋กœํŠธ ๋ฒˆํ˜ธ๋‚˜ ๋ฐฐ์น˜ ๋ฒˆํ˜ธ๋กœ ํŠน์ • ์ธ์ฆ์„œ๋ฅผ ์ฐพ์„ ์ˆ˜ ์žˆ์Šต๋‹ˆ๋‹ค.

์ด ์ œํ’ˆ์„ ์ด๋ฏธ ๊ฐ€์ง€๊ณ  ๊ณ„์‹ญ๋‹ˆ๊นŒ?

๋ฌธ์„œ ๋ผ์ด๋ธŒ๋Ÿฌ๋ฆฌ์—์„œ ์ตœ๊ทผ์— ๊ตฌ๋งคํ•œ ์ œํ’ˆ์— ๋Œ€ํ•œ ๋ฌธ์„œ๋ฅผ ์ฐพ์•„๋ณด์„ธ์š”.

๋ฌธ์„œ ๋ผ์ด๋ธŒ๋Ÿฌ๋ฆฌ ๋ฐฉ๋ฌธ

์ด๋ฏธ ์—ด๋žŒํ•œ ๊ณ ๊ฐ

Slide 1 of 5

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Tetrabutylphosphonium bromide 98%

Sigma-Aldrich

189138

Tetrabutylphosphonium bromide

Tetramethylammonium bromide 98%

Sigma-Aldrich

195758

Tetramethylammonium bromide

Cetrimonium bromide United States Pharmacopeia (USP) Reference Standard

USP

1102974

Cetrimonium bromide

Tetrabutylammonium bromide ReagentPlus®, ≥99.0%

Sigma-Aldrich

193119

Tetrabutylammonium bromide

Tetrabutylammonium chloride ≥97.0% (NT)

Sigma-Aldrich

86870

Tetrabutylammonium chloride

Quaternary Ammonium Salts as Alkylating Reagents in C-H Activation Chemistry.
Spettel M, et al.
Organic Letters, 19(16), 4287-4290 (2017)
Chemical modification of polymers via phase transfer catalysis
Nishikubo T.
Handbook of Phase Transfer Catalysis, 480-509 (1997)
Novel catalyst based on Co-complex to prepare MWCNT.
Alonso-Nu?ez G, et al.
Materials Letters, 109, 163-166 (2013)
Quaternary ammonium salts as highly efficient and green alkylating agents for N-alkylation of azaheterocycles under microwave irradiation.
Khalafi-Nezhad A, et al.
Journal of the Iranian Chemical Society, 5(1), S40-S46 (2008)
The electrochemical synthesis of the graphite intercalation compounds containing tetra-n-alkylammonium cations.
Sirisaksoontorn W and Lerner MM.
Journal of Sol-Gel Science and Technology, 2(9), M28-M32 (2013)

์ž์‚ฌ์˜ ๊ณผํ•™์žํŒ€์€ ์ƒ๋ช… ๊ณผํ•™, ์žฌ๋ฃŒ ๊ณผํ•™, ํ™”ํ•™ ํ•ฉ์„ฑ, ํฌ๋กœ๋งˆํ† ๊ทธ๋ž˜ํ”ผ, ๋ถ„์„ ๋ฐ ๊ธฐํƒ€ ๋งŽ์€ ์˜์—ญ์„ ํฌํ•จํ•œ ๋ชจ๋“  ๊ณผํ•™ ๋ถ„์•ผ์— ๊ฒฝํ—˜์ด ์žˆ์Šต๋‹ˆ๋‹ค..

๊ณ ๊ฐ์ง€์›ํŒ€์œผ๋กœ ์—ฐ๋ฝ๋ฐ”๋ž๋‹ˆ๋‹ค.