16980
2-Bromododecanoic acid
≥98.0%
Synonym(s):
2-Bromolauric acid
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About This Item
Linear Formula:
CH3(CH2)9CHBrCOOH
CAS Number:
Molecular Weight:
279.21
Beilstein:
1774990
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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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