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Merck
CN

249416

2-Ethylhexyl bromide

contains 1% potassium carbonate as stabilizer, 95%

Synonym(s):

1-Bromo-2-ethylhexane

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About This Item

Linear Formula:
CH3(CH2)3CH(C2H5)CH2Br
CAS Number:
18908-66-2
Molecular Weight:
193.12
NACRES:
NA.22
PubChem Substance ID:
24854990
UNSPSC Code:
12352100
MDL number:
MFCD00000220
Assay:
95%
Form:
liquid

Key Documents

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InChI

1S/C8H17Br/c1-3-5-6-8(4-2)7-9/h8H,3-7H2,1-2H3

SMILES string

CCCCC(CC)CBr

InChI key

NZWIYPLSXWYKLH-UHFFFAOYSA-N

assay

95%

form

liquid

contains

1% potassium carbonate as stabilizer

refractive index

n20/D 1.4538 (lit.)

bp

75-77 °C/16 mmHg (lit.)

density

1.086 g/mL at 25 °C (lit.)

functional group

alkyl halide, bromo

storage temp.

2-8°C

Quality Level

100

Related Categories

Application

2-Ethylhexyl bromide has been used in the synthesis of:
  • methoxy-4-(2-ethylhexyloxy)benzene
  • photovoltaic conjugated polymer, having benzo[1,2-b:4,5-b′]difuran building block
  • 1-bromo-4-(2′-ethylhexyloxy)benzene3

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

156.2 °F - closed cup

flash_point_c

69 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCT3155
MKCN2939
MKCJ7206
MKCG4406
MKBZ1138V

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MEH-PPV: improved synthetic procedure and molecular weight control.
Neef CJ and Ferraris JP.
Macromolecules, 33(7), 2311-2314 (2000)
Lijun Huo et al.
Chemical communications (Cambridge, England), 48(27), 3318-3320 (2012-03-01)
A new building block of benzo[1,2-b:4,5-b']difuran (BDF) was firstly designed and synthesized. The newly designed unit was applied for constructing a new photovoltaic low band gap polymer, PBDFDTBT, which exhibited promising power conversion efficiency of 5.0%.
Siva Doddi et al.
Journal of fluorescence, 26(6), 1939-1949 (2016-11-01)
We report the synthesis and characterization of a new fluorescent dyad SP-DPP-SP(9) via efficient palladium-catalyzed Sonogashira coupling of prop-2-yn-1-yl 3-(3',3'dimethyl-6-nitrospiro[chromene-2,2'-indolin]-1'-yl)propanoatespiropyran, SP(8), a well known photochromic accepter, with 3,6-bis(5-bromothiophen-2-yl)-2,5-bis((R)-2-ethylhexyl)-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-dione, DPP(4), a highly fluorescent donor. Under visible light exposure the SP unit
Efficient 9-alkylphenyl-9-pyrenylfluorene substituted pyrene derivatives with improved hole injection for blue light-emitting diodes.
Tang C, et al.
Journal of Materials Chemistry, 16(41), 4074-4080 (2006)
Kavya S Keremane et al.
Photochemistry and photobiology, 97(2), 289-300 (2020-10-02)
Developing effective and low-cost organic hole-transporting materials (HTMs) is crucial for the construction of high-performance perovskite solar cells (PSCs) and to promote their production in commercial ventures. In this context, we herein report the molecular design, synthesis and characterization of
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