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Thermo Scientific Chemicals
Bromoacetic acid, 98+%
CAS: 79-08-3 | C2H3BrO2 | 138.948 g/mol
化学物質識別子
CAS79-08-3
IUPAC Name2-bromoacetic acid
Molecular FormulaC2H3BrO2
InChI KeyKDPAWGWELVVRCH-UHFFFAOYSA-N
SMILESOC(=O)CBr
さらに表示
仕様
スペックシート
スペックシートAssay (Aqueous acid-base Titration)≥98.0 to ≤102.0%
FormCrystals or powder or crystalline powder or fused solid
Water Content (Karl Fischer Titration)≤1%
Appearance (Color)White to cream to yellow to pale brown
Assay (Silylated GC)≥98.0%
Bromoacetic acid is used in organic synthesis and as an alkylating agent. It is also used as a biochemical for proteomics research. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, dyes and agrochemicals.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Bromoacetic acid is used in organic synthesis and as an alkylating agent. It is also used as a biochemical for proteomics research. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, dyes and agrochemicals.
Solubility
Soluble in water, alcohol
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. It is hygroscopic in nature and sensitive to light and air. Handle and store under inert gas. Incompatible with strong oxidizing agents and strong bases.
Bromoacetic acid is used in organic synthesis and as an alkylating agent. It is also used as a biochemical for proteomics research. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, dyes and agrochemicals.
Solubility
Soluble in water, alcohol
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. It is hygroscopic in nature and sensitive to light and air. Handle and store under inert gas. Incompatible with strong oxidizing agents and strong bases.
RUO – Research Use Only
General References:
- E.A. Barnard.; W.D. Stein. The histidine residue in the active centre of ribonuclease: I. A specific reaction with bromoacetic acid. Journal of Molecular Biology. 1959, 1 (4-5), 339-349.
- Philip J. Elving.; Isadore Rosenthal.; Marilyn Koll Kramer. Polarographic Behavior of Organic Compounds. IX. Iodoacetic Acid and the Bromoacetic Acids. J. Am. Chem. Soc. 1951, 73 (4), 1717-1722.
- Reaction with a dialkyl phosphite followed by an aldehyde has been used in a convenient one-pot synthesis of acrylic acids: J. Org. Chem., 46, 2514 (1981). For examples with reaction schemes, see Chloroacetic acid, A11482 and 2-Bromopropionic acid, A17569.