Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

33056-U

Supelco

BCl3-2-Chloroethanol

10 % (w/w), pkg of 10 × 1 mL

Synonym(s):

Boron trichloride

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

UNSPSC Code:
41115710

grade

derivatization grade ((GC derivatization))

description

Esterification reagent

reaction suitability

reagent type: derivatization reagent
reaction type: Esterifications

packaging

pkg of 10 × 1 mL
box of 10 ampules (1mL each)

concentration

10 % (w/w)

storage temp.

2-8°C

General description

BCl3-2-Chloroethanol is a derivatizing reagent. It helps in forming methyl esters. It is considered less toxic in nature.[1]

Application

BCl3-2-Chloroethanol may be used as derivatizing reagent for determination of 2,4-dichlorophenoxyacetic acid using GC-ECD.[1]

Other Notes

Reagent for 2-chloroethyl ester.

signalword

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 1 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1 - Repr. 1B - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

138.2 °F - closed cup

flash_point_c

59 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support.

Already Own This Product?

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

Visit the Document Library

An improved gas chromatographic method for the analysis of 2,4-D free acid in soil.
D W Woodham et al.
Journal of agricultural and food chemistry, 19(1), 186-188 (1971-01-01)
K C Ting et al.
Journal of AOAC International, 81(1), 93-98 (1998-03-21)
2,4-Dichlorophenoxyacetic acid (2,4-D) residues in fresh produce is officially analyzed as its methyl ester form by gas chromatography with electron capture detection (GC-ECD). Because of safety concerns with diazomethane, the reagent used to form methyl esters, a less toxic and

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service