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B65551

Sigma-Aldrich

1-Bromododecane

97%

Synonym(s):

Dodecyl bromide, Lauryl bromide

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About This Item

Linear Formula:
CH3(CH2)11Br
CAS Number:
143-15-7
Molecular Weight:
249.23
Beilstein/REAXYS Number:
506159
EC Number:
205-587-9
MDL number:
MFCD00000225
UNSPSC Code:
12352100
PubChem Substance ID:
24891918
NACRES:
NA.22

vapor density

8.6 (vs air)

Quality Level

200

assay

97%

form

liquid

refractive index

n20/D 1.458 (lit.)

bp

134-135 °C/6 mmHg (lit.)

mp

−11-−9 °C (lit.)

density

1.038 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCCCBr

InChI

1S/C12H25Br/c1-2-3-4-5-6-7-8-9-10-11-12-13/h2-12H2,1H3

InChI key

PBLNBZIONSLZBU-UHFFFAOYSA-N

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Application

1-Bromododecane can be used for modifying the solubility and processability by alkylation. Some of the reported applications include:
  • Improving the solubility of rigid polycyclic aromatic hydrocarbons used in organic electronics to ease the solution processability.[1][2][3]
  • Inducing hydrophobicity ethoxylated urethanes and polyurethanes.[4][5]
  • Increasing lipophilicity of molecules for biological applications.[6][7]

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315

Hazard Classifications

Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

230.0 °F

flash_point_c

110 °C

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCS4158
MKCV3683
0000225480
MKCM1801
MKCL5045

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Rinku Dutta et al.
Pharmaceutical research, 34(3), 564-578 (2016-12-21)
To determine the pharmacokinetic parameters and biodistribution of GDC-0449 loaded polymeric micelles after systemic administration into common bile duct ligation (CBDL) induced liver fibrotic mice. We used GDC-0449 encapsulated methoxy poly (ethylene glycol)-block-poly (2-methyl-2-carboxyl-propylene carbonate)-graft-dodecanol (PEG-PCD) non-targeted polymeric micelles for
Influence of substituted structure of Percec-type mini-dendritic end groups on aggregation and rheology of hydrophobically modified ethoxylated urethanes (HEURs) in aqueous solution.
Du Z, et al.
Polymer, 135, 131-141 (2018)
Surface hydrophobic modification of polyurethanes by diaryl carbene chemistry: Synthesis and characterization.
Yang P, et al.
Applied Surface Science, 435, 346-351 (2018)
Contorted polycyclic aromatic hydrocarbons with cove regions and zig-zag edges.
Chen Y, et al.
Chemical Communications (Cambridge, England), 53(60), 8474-8477 (2017)
Synthesis and Properties of New N?Heteroheptacenes for Solution?Based Organic Field Effect Transistors.
Zhou F, et al.
Chemistry?A European Journal , 23(51), 12542-12549 (2017)
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