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CAS RN: 99-73-0 | Product Number: A5501
4-Bromophenacyl Bromide [for HPLC Labeling]
Purity: >99.0%(T)
Synonyms:
- 2,4'-Dibromoacetophenone
Product Documents:
Size | Unit Price | Shanghai | Tianjin | Japan* |
---|---|---|---|---|
5G |
¥895.00
|
1 | Contact Us | 6 |
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Product Number | A5501 |
Purity / Analysis Method | >99.0%(T) |
Molecular Formula / Molecular Weight | C__8H__6Br__2O = 277.94 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Refrigerated (0-10°C) |
Condition to Avoid | Light Sensitive,Heat Sensitive |
CAS RN | 99-73-0 |
Reaxys Registry Number | 607604 |
PubChem Substance ID | 87563151 |
SDBS (AIST Spectral DB) | 1752 |
Merck Index (14) | 1427 |
MDL Number | MFCD00000200 |
Specifications
Appearance | White to Almost white powder to crystal |
Purity(Argentometric Titration) | min. 99.0 % |
Melting point | 109.0 to 112.0 °C |
Solubility in Toluene | almost transparency |
Effect test of HPLC derivatization | Effective as labeling agent for Hexanoic Acid. |
Properties (reference)
Melting Point | 111 °C |
Solubility (soluble in) | Toluene |
GHS
Pictogram | |
Signal Word | Danger |
Hazard Statements | H314 : Causes severe skin burns and eye damage. H290 : May be corrosive to metals. |
Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P260 : Do not breathe dusts or mists. P234 : Keep only in original container. P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection. P390 : Absorb spillage to prevent material damage. P303 + P361 + P353 : IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water/shower. P301 + P330 + P331 : IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. P363 : Wash contaminated clothing before reuse. P304 + P340 + P310 : IF INHALED: Remove person to fresh air and keep comfortable for breathing. Immediately call a POISON CENTER/doctor. P305 + P351 + P338 + P310 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Immediately call a POISON CENTER/doctor. P406 : Store in corrosive resistant container with a resistant inner liner. P405 : Store locked up. |
Related Laws:
CN Number | 2384 |
RTECS# | AM6950000 |
Transport Information:
UN Number | UN3261 |
Class | 8 |
Packing Group | III |
Customs Control Conditions (Q) |
Application
HPLC Labeling Reagent for Carboxylic Acids
The compound 1 is an HPLC labeling reagent, which has a bromoacetyl group and easily reacts with a carboxyl group to form the corresponding ester in the presence of a base. The resultant ester is stable and can reach the detector without any decomposition under reversed phase HPLC. An excellent chromatogram can be obtained by measuring at 254 nm, an absorption wavelength that is generally used for UV detection.
Application examples:
[Fatty acids]1, 2, 8, 9)
Dissolve a sample in methanol or water, and then neutralize the sample solution with methanol solution of KOH-crown ether. Evaporate to dryness under reduced pressure, and then you will see a generally almost white solid substance remaining (potassium salt of fatty acid). Next, add the HPLC labeling reagent 1 with acetonitrile solution* of 18-crown 6-ether to this white solid and further add acetonitrile for a volume up to 10 mL. Incubate the solution at 80 °C for 15 min. Cool the resultant solution to room temperature and use it as an HPLC sample.
* Benzene can be used in the place of acetonitrile. The mixing ratio (molar ratio) for the HPLC labeling reagent 1 and 18-crown 6-ether should be 20 to 1 and 10 to 1 for the sample fatty acid concentrations at 0.5~20 mM and less than 0.5 mM, respectively. Use the excessive amount of the reagent 1.
[Others]
Dicarboxyl acids2), synthetic prostaglandins3), unsaturated fatty acids4), alkyl methylphosphonate5), ganglioside6), betaine7)
[Fatty acids]1, 2, 8, 9)
Dissolve a sample in methanol or water, and then neutralize the sample solution with methanol solution of KOH-crown ether. Evaporate to dryness under reduced pressure, and then you will see a generally almost white solid substance remaining (potassium salt of fatty acid). Next, add the HPLC labeling reagent 1 with acetonitrile solution* of 18-crown 6-ether to this white solid and further add acetonitrile for a volume up to 10 mL. Incubate the solution at 80 °C for 15 min. Cool the resultant solution to room temperature and use it as an HPLC sample.
* Benzene can be used in the place of acetonitrile. The mixing ratio (molar ratio) for the HPLC labeling reagent 1 and 18-crown 6-ether should be 20 to 1 and 10 to 1 for the sample fatty acid concentrations at 0.5~20 mM and less than 0.5 mM, respectively. Use the excessive amount of the reagent 1.
[Others]
Dicarboxyl acids2), synthetic prostaglandins3), unsaturated fatty acids4), alkyl methylphosphonate5), ganglioside6), betaine7)
TCI Products Pamphlet
HPLC Labeling Reagents ( PDF 10MB )
HPLC Labeling Reagents ( PDF 10MB )
References
- 1)H. D. Durst, Anal. Chem. 1975, 47, 1797.
- 2)E. Grushka, J. Chromatogr. 1975, 112, 673.
- 3)F. A. Fitzpatrick, Anal. Chem. 1976, 48, 499.
- 4)Y. Suzuki, T. Takeuchi, Nihon Gakujutsu Shinkoukai Tanka Suiso Kagaku Dai 116 Iinkai Gyoseki Houkoku 1976, 29, 152.
- 5)P. C. Bossle, J. J. Martin, E. W. Sarver, H. Z. Sommer, J. Chromatogr. 1983, 267, 209.
- 6)H. Nakabayashi, M. Iwamori, Y. Nagai, J. Biochem. 1984, 96, 977.
- 7)S. Konosu, A. Shinagawa, K. Yamaguchi, Bull. Jpn. Soc. Sci. Fisher. 1986, 52, 869.
- 8)M. Alberghina, A. Fiumara, L. Pavone, A. M. Giuffrida, Neurochem. Res. 1984, 9, 1719.
- 9)K. Kihara, S. Rokushika, H. Hatano, Bunseki Kagaku 1984, 33, 647.
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