33353
Boron trichloride - Methanol
12 % (w/w), pkg of 20 × 1 mL
Synonym(s):
BCl3
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About This Item
UNSPSC Code:
41116105
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description
Esterification reagent
reaction suitability
reagent type: derivatization reagent
reaction type: Esterifications
packaging
pkg of 20 × 1 mL
concentration
12 % (w/w)
storage temp.
2-8°C
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General description
Boron trichloride-methanol is a derivatizing reagent. It is basically used in the esterification of fatty acids to fatty acid methyl ester (FAME).
Application
Boron trichloride-Methanol may be used in converting Linoleate to methyl linoleate for understanding the effect of palmitic acid on oxidation of oleic acid.[1]
Other Notes
Reagent for methyl ester, pentafluoropropionyl.
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Description
Pricing
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Danger
Hazard Classifications
Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Eye Dam. 1 - Flam. Liq. 2 - Repr. 1B - Skin Corr. 1B - STOT SE 1
target_organs
Eyes,Central nervous system
supp_hazards
Storage Class
3 - Flammable liquids
wgk_germany
WGK 3
flash_point_f
51.8 °F - closed cup
flash_point_c
11 °C - closed cup
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E. Gelpi et al
Journal of Chromatography A, 12, 701-701 (1974)
J.Segura et al.
Biomedical Mass Spectrometry, 3, 91-91 (1971)
D.R. Knapp
Handbook of Analytical Derivatization Reactions, 218-218 (1979)
J M Onorato et al.
The Journal of biological chemistry, 275(28), 21177-21184 (2000-05-10)
Maillard or browning reactions lead to formation of advanced glycation end products (AGEs) on protein and contribute to the increase in chemical modification of proteins during aging and in diabetes. AGE inhibitors such as aminoguanidine and pyridoxamine (PM) have proven
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