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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
Pricing and availability is not currently available.

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

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Anti-HDAC4 Antibody

biological source

mouse

biological source

mouse

biological source

rabbit

biological source

rabbit

clone

3F3, monoclonal

clone

2E10, monoclonal

clone

polyclonal

clone

polyclonal

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

serum

species reactivity

bovine, human, hamster, rat, mouse

species reactivity

mouse, human

species reactivity

rat, human, mouse

species reactivity

human

UniProt accession no.

Q92769

UniProt accession no.

O09106

UniProt accession no.

Q13547

UniProt accession no.

P56524

Gene Information

human ... HDAC2(3066)

Gene Information

human ... HDAC1(3065)
mouse ... Hdac1(433759)

Gene Information

human ... HDAC1(3065)
mouse ... Hdac1(433759)
rat ... Hdac1(297893)

Gene Information

human ... HDAC4(9759)

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
    MKCM1801
    MKCL5045
    MKCF2449
    MKBZ9610V
    MKBT7715V

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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)
    Solution-processable 2,1,3-benzothiadiazole containing compound based on the novel 1-dodecyl-6-dodecoxynaphthyridine-2-one unit for organic field-effect transistors.
    Cameron J, et al.
    Organic Electronics, 49, 400-405 (2017)
    Contorted polycyclic aromatic hydrocarbons with cove regions and zig-zag edges.
    Chen Y, et al.
    Chemical Communications (Cambridge, England), 53(60), 8474-8477 (2017)
    View All Related Papers

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