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200999

Sigma-Aldrich

12-Bromododecanoic acid

97%

Sinônimo(s):

12-Bromolauric acid

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About This Item

Fórmula linear:
Br(CH2)11CO2H
Número CAS:
73367-80-3
Peso molecular:
279.21
Beilstein:
1771588
Número CE:
277-401-4
Número MDL:
MFCD00002738
Código UNSPSC:
12352100
ID de substância PubChem:
24851988
NACRES:
NA.22

Ensaio

97%

pf

52-55 °C (lit.)

solubilidade

chloroform: soluble 50 mg/mL, clear to slightly hazy, colorless to faintly yellow

cadeia de caracteres SMILES

OC(=O)CCCCCCCCCCCBr

InChI

1S/C12H23BrO2/c13-11-9-7-5-3-1-2-4-6-8-10-12(14)15/h1-11H2,(H,14,15)

chave InChI

YYKBWYBUCFHYPR-UHFFFAOYSA-N

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Aplicação

12-Bromododecanoic acid ligand was used as a model fatty acid in the elucidation of the x-ray structure of bovine beta-lactoglobulin.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

230.0 °F - closed cup

Ponto de fulgor (°C)

110 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

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S Modi et al.
Biochemistry, 34(28), 8982-8988 (1995-07-18)
The binding of the substrates sodium laurate and sodium 12-bromolaurate to the heme-containing domain of Bacillus megaterium cytochrome P450 BM3 (CYP102) has been studied by measurement of the relaxation effects of the unpaired electrons of the heme iron on the
A simple synthesis of bromine-77-labeled alkyl bromides.
M R Kilbourn et al.
The International journal of applied radiation and isotopes, 33(5), 391-392 (1982-05-01)
G C Roberts
Neurochemical research, 21(9), 1117-1124 (1996-09-01)
NMR spectroscopy has proved to be a valuable tool in the study of the interactions between enzymes and their substrates. The kinds of structural and dynamic information which can be obtained are illustrated by studies of three enzymes involved in
B Y Qin et al.
FEBS letters, 438(3), 272-278 (1998-11-25)
The X-ray structure of bovine beta-lactoglobulin with the ligand 12-bromododecanoic acid as a model for fatty acids has been determined at a resolution of 2.23 A in the trigonal lattice Z form. The ligand binds inside the calyx, resolving a
Xiang He et al.
The Journal of biological chemistry, 280(24), 22697-22705 (2005-04-26)
The fatty acid omega-hydroxylation regiospecificity of CYP4 enzymes may result from presentation of the terminal carbon to the oxidizing species via a narrow channel that restricts access to the other carbon atoms. To test this hypothesis, the oxidation of 12-iodo-
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