Ethyl hexafluoroglutaryl chloride, 97%, Thermo Scientific Chemicals
Ethyl hexafluoroglutaryl chloride, 97%, Thermo Scientific Chemicals
Thermo Scientific™

Ethyl hexafluoroglutaryl chloride, 97%, Thermo Scientific Chemicals

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Quantity:
5 g
Catalog number L14049.06
also known as L14049-06
Price (USD)/ Each
364.00
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Quantity:
5 g
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Price (USD)/ Each
364.00
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Ethyl hexafluoroglutaryl chloride, 97%, Thermo Scientific Chemicals
Catalog numberL14049.06
Price (USD)/ Each
364.00
-
Add to cart
Specifications
Chemical Name or MaterialEthyl hexafluoroglutaryl chloride
CAS18381-53-8
Health Hazard 1H314-H335
Health Hazard 2GHS H Statement
H314-H318
Causes severe skin burns and eye damage.
Causes serious eye damage.
Health Hazard 3P260-P264b-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P501c
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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.
RUO – Research Use Only

General References:

  1. 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.
  2. 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.