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16980

Sigma-Aldrich

2-Bromododecanoic acid

≥98.0%

Synonym(s):

2-Bromolauric acid

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About This Item

Linear Formula:
CH3(CH2)9CHBrCOOH
CAS Number:
111-56-8
Molecular Weight:
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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Certificates of Analysis (COA)

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

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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
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
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