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Merck
CN

18628

11-溴十一酸

purum, ≥98.0% (GC)

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线性分子式:
Br(CH2)10COOH
化学文摘社编号:
分子量:
265.19
EC Number:
220-602-9
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
1767205
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grade

purum

assay

≥98.0% (GC)

bp

173-174 °C/2 mmHg (lit.)

mp

45-48 °C (lit.), 48-51 °C

SMILES string

OC(=O)CCCCCCCCCCBr

InChI

1S/C11H21BrO2/c12-10-8-6-4-2-1-3-5-7-9-11(13)14/h1-10H2,(H,13,14)

InChI key

IUDGNRWYNOEIKF-UHFFFAOYSA-N

General description

11-Bromoundecanoic acid reacts with potassium salt of dimethyl hydantoin to yield 4,4-dimethyl hydantoin-undecanoic acid.

Application

11-Bromoundecanoic acid was used in the synthesis of:
  • 11-phenoxyundecyl phosphate
  • [13,14-2H2]-11-hydroxytetradecanoic acid
  • new acrylate-based cationic reactive surfactants


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存储类别

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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Synthesis of new acrylate-based cationic surfmers and their use in the synthesis of PMMA-clay nanocomposite via heterophase polymerization.
Morizur J-F and Mathias LJ.
Polymer Preprints (American Chemical Society, Division of Polymer Chemistry), 48(1), 340-340 (2007)
Revathi V Padmanabhuni et al.
Industrial & engineering chemistry research, 51(14), 5148-5156 (2012-09-04)
The purpose of this study was to demonstrate that the surface of CaCO(3) fillers could be coated with an N-halamine based fatty acid to make the filler surface organophilic and accomplish antibacterial activity simultaneously, rendering the resulting polymer-filler composites antimicrobial.
I Navarro et al.
Bioorganic & medicinal chemistry, 4(3), 439-443 (1996-03-01)
The synthesis of deuterium labeled 11- and 12-hydroxytetradecanoic acids to study a (11E) desaturase in the moth Spodoptera littoralis is reported. [14,14,14-2H3] 12-hydroxytetradecanoic acid was synthesized in four steps from 11-iodo-1-undecene in 49% overall yield. Deuterium was introduced by reaction