Skip to Content
Merck
CN

33033

Boron trichloride - Methanol

12 % (w/w), pkg of 400 mL

Synonym(s):

BCl3

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

UNSPSC Code:
41116105
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


reaction suitability

reagent type: derivatization reagent
reaction type: Esterifications

packaging

pkg of 400 mL

concentration

12 % (w/w)

storage temp.

2-8°C

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.

Other Notes

Reagent for methyl ester, pentafluoropropionyl.


Still not finding the right product?

Explore all of our products under Boron trichloride - Methanol


signalword

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

WGK 3

flash_point_f

51.8 °F - closed cup

flash_point_c

11 °C - closed cup

Regulatory Information

监管及禁止进口产品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



J.Segura et al.
Biomedical Mass Spectrometry, 3, 91-91 (1971)
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
Gas chromatography-mass spectrometry of catecholamines and tryptamines: determination of gas chromatographic profiles of the amines, their precursors and their metabolites.
E G Peralta et al.
Journal of chromatographic science, 12(11), 701-709 (1974-11-01)



Global Trade Item Number

SKUGTIN
3303304061837810688