Date published: 2025-12-17

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2-Bromododecanoic acid (CAS 111-56-8)

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Alternate Names:
2-Bromolauric acid; Dodecanoic acid
Application:
2-Bromododecanoic acid is used in the synthesis of carboxylic amphoteric surfactants
CAS Number:
111-56-8
Purity:
≥97%
Molecular Weight:
279.21
Molecular Formula:
C12H23BrO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2-Bromododecanoic acid functions as an inhibitor in certain biochemical reactions. It acts by binding to specific enzymes or proteins, thereby disrupting their normal function and inhibiting the progression of the reaction. This disruption occurs at the molecular level, where the 2-Bromododecanoic acid′s structure allows it to interact with the active site of the enzyme or protein, preventing the substrate from binding and inhibiting the catalytic activity. 2-Bromododecanoic Acid′s mechanism of action involves interfering with the normal progression of the reaction, ultimately leading to a decrease in the production of the desired product. In this way, 2-Bromododecanoic acid plays a role in modulating the activity of specific enzymes or proteins within experimental applications.


2-Bromododecanoic acid (CAS 111-56-8) References

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  2. Calcium mobilisation and CCK secretion induced by modified fatty acids and latex microspheres reveal dual receptor mechanisms for lipid stimulation of STC-1 cells.  |  Kazmi, S., et al. 2003. J Physiol. 553: 759-73. PMID: 14555726
  3. Physicochemical properties of anionic triple-chain surfactants in alkaline solutions.  |  Yoshimura, T. and Esumi, K. 2004. J Colloid Interface Sci. 276: 450-5. PMID: 15271573
  4. Synthesis of amphiphilic derivatives of rose bengal and their tumor accumulation.  |  Sugita, N., et al. 2007. Bioconjug Chem. 18: 866-73. PMID: 17367181
  5. Oral absorption enhancement of dipeptide L-Glu-L-Trp-OH by lipid and glycosyl conjugation.  |  Bergeon, JA., et al. 2008. Biopolymers. 90: 633-43. PMID: 18428206
  6. Ester Formation via Symbiotic Activation Utilizing Trichloroacetimidate Electrophiles.  |  Mahajani, NS., et al. 2019. J Org Chem. 84: 7871-7882. PMID: 31117564
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  8. Chiral discrimination by albumin: a mechanistic study of liquid chromatographic optical resolution of nonaromatic carboxylic acids.  |  Allenmark, S. 1993. Chirality. 5: 295-9. PMID: 8398590
  9. Involvement of carnitine acyltransferases in peroxisomal fatty acid metabolism by the yeast Pichia guilliermondii.  |  Pagot, Y. and Belin, JM. 1996. Appl Environ Microbiol. 62: 3864-7. PMID: 8837442
  10. Evaluation of Selective Interaction of Ga3+ with N-Octadecanoyl-N-phenylhydroxylamine by L-B Technique.  |  Okushita, H. and Shimidzu, T. 1996. J Colloid Interface Sci. 183: 315-9. PMID: 8954669
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Bromododecanoic acid, 5 g

sc-223434
5 g
$55.00