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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-882-7
Beilstein/REAXYS Number:
1774990
MDL number:
InChI key
HXKXBCBZXXQPPD-UHFFFAOYSA-N
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)
SMILES string
CCCCCCCCCCC(Br)C(O)=O
assay
≥98.0%
form
solid
solubility
methanol: soluble 1 g/10 mL, clear, colorless
storage temp.
2-8°C
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Y Pagot et al.
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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
Synthesis and properties of amphoteric surfactants.
Gawish SM, et al.
Journal of the American Oil Chemists' Society, 58(6), 757-760 (1981)
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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
K S Echtay et al.
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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
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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