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16980

Sigma-Aldrich

2-Bromododecanoic acid

≥98.0%

Sinónimos:

2-Bromolauric acid

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About This Item

Fórmula lineal:
CH3(CH2)9CHBrCOOH
Número de CAS:
111-56-8
Peso molecular:
279.21
Beilstein/REAXYS Number:
1774990
EC Number:
203-882-7
MDL number:
MFCD00021693
UNSPSC Code:
12352100
PubChem Substance ID:
57647595
NACRES:
NA.22

assay

≥98.0%

form

solid

mp

30-32 °C

solubility

methanol: soluble 1 g/10 mL, clear, colorless

storage temp.

2-8°C

SMILES string

CCCCCCCCCCC(Br)C(O)=O

InChI

1S/C12H23BrO2/c1-2-3-4-5-6-7-8-9-10-11(13)12(14)15/h11H,2-10H2,1H3,(H,14,15)

InChI key

HXKXBCBZXXQPPD-UHFFFAOYSA-N

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Application

2-Bromododecanoic acid was used in the synthesis of carboxylic amphoteric surfactants containing ether tertiary amino and carboxylic groups. It was also used in the synthesis of C12-lipoamino acid.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
1290012V
1290012
035806/1
1196871
35806/1

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Synthesis and properties of amphoteric surfactants.
Gawish SM, et al.
Journal of the American Oil Chemists' Society, 58(6), 757-760 (1981)
Y Pagot et al.
Applied and environmental microbiology, 62(10), 3864-3867 (1996-10-01)
This article provides information about peroxisomal fatty acid metabolism in the yeast Pichia guilliermondii. The existence of inducible mitochondrial carnitine palmitoyltransferase and peroxisomal carnitine octanoyl-transferase activities was demonstrated after culture of this yeast in a medium containing methyl oleate. The
Ying-Shan Chen et al.
Journal of pharmaceutical sciences, 102(7), 2322-2331 (2013-05-23)
Optic neuropathy is associated with retinal ganglion cell (RGC) loss leading to optic nerve damage and visual impairment. Unregulated connexin (Cx) hemichannel opening plays a role in RGC loss. Thus, inhibition via Cx43-specific mimetic peptides (MP) may prevent further cell
S S Sidhu et al.
The Journal of physiology, 528 Pt 1, 165-176 (2000-10-06)
1. Fatty acid-induced cholecystokinin (CCK) secretion in humans and from the enteroendocrine cell line STC-1 depends critically on acyl chain length. 2. Therefore we have characterized the relationship between acyl chain length and the potency of the fatty acid to
K S Echtay et al.
Biochemistry, 40(17), 5243-5248 (2001-04-25)
The functional role of the four intrahelical arginines in uncoupling protein (UCP1) from brown adipose tissue were studied in mutants where they were replaced by noncharged residues. Wild-type and mutant UCP1 were expressed in Saccharomyces cerevisiae. As measured in isolated
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