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Ethyl hexafluoroglutaryl chloride, 97%, Thermo Scientific Chemicals
仕様
化学物質名または材質Ethyl hexafluoroglutaryl chloride
CAS18381-53-8
健康被害1H314-H335
健康被害2GHS H Statement
H314-H318
Causes severe skin burns and eye damage.
Causes serious eye damage.
H314-H318
Causes severe skin burns and eye damage.
Causes serious eye damage.
健康被害3P260-P264b-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P501c
さらに表示
Ethyl hexafluoroglutaryl chloride is used as a derivatising agent in gas chromatography. It is an active reagent used for the quantization of amphetamine and methamphetamine in urine by gas chromatography/mass spectroscopy (GC/MS).
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
Ethyl hexafluoroglutaryl chloride is used as a derivatising agent in gas chromatography. It is an active reagent used for the quantization of amphetamine and methamphetamine in urine by gas chromatography/mass spectroscopy (GC/MS).
Solubility
Miscible with water.
Notes
Moisture sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents, bases and water.
Ethyl hexafluoroglutaryl chloride is used as a derivatising agent in gas chromatography. It is an active reagent used for the quantization of amphetamine and methamphetamine in urine by gas chromatography/mass spectroscopy (GC/MS).
Solubility
Miscible with water.
Notes
Moisture sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents, bases and water.
RUO – Research Use Only
General References:
- Pace, A.; Buscemi, S.; Vivona, N. The synthesis of fluorinated heteroaromatic compounds. Part 1. Five-membered rings with more than two heteroatoms. Org. Prep. Proc. Int. 2005, 37 (5), 447-506.
- Prakash, G. S.; Hu, J.; Olah, G. A. Alkylation of in situ generated fluorinated alkoxides: novel synthesis of partially fluorinated ethers. Arkivoc 2003, 3, 104-119.