Skip to Content
Merck
CN

357480

2-Methoxyethoxymethyl chloride

technical grade

Synonym(s):

β-Methoxyethoxymethyl chloride, MEM-chloride

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
CH3OCH2CH2OCH2Cl
CAS Number:
3970-21-6
Molecular Weight:
124.57
UNSPSC Code:
12352101
NACRES:
NA.22
PubChem Substance ID:
24861920
MDL number:
MFCD00000888
Beilstein/REAXYS Number:
1900576

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

2-Methoxyethoxymethyl chloride, technical grade

InChI

1S/C4H9ClO2/c1-6-2-3-7-4-5/h2-4H2,1H3

SMILES string

COCCOCCl

InChI key

BIAAQBNMRITRDV-UHFFFAOYSA-N

grade

technical grade

form

liquid

refractive index

n20/D 1.427 (lit.)

bp

50-52 °C/13 mmHg (lit.)

density

1.091 g/mL at 25 °C (lit.)

functional group

chloro
ether

storage temp.

2-8°C

Quality Level

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

OH-protecting reagent. MEM ethers are stable to a variety of reaction conditions and are selectively cleaved under aprotic conditions in the presence of a wide rangeof OH-protected moieties.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 1A - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

129.2 °F - closed cup

flash_point_c

54 °C - closed cup

ppe

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

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCN4333
BCCM3224
BCCH4596
BCCG1365
BCCD8899

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

The Journal of Organic Chemistry, 59, 1011-1011 (1994)
Protection of uracil residue with methoxyethoxymethyl group.
T Ito et al.
Nucleic acids symposium series, (12)(12), 51-54 (1983-01-01)
Synthesis of oligoribonucleotides using the methoxyethoxymethyl group as the protecting groups of the base residues and the hydroxyl functions.
T Ito et al.
Nucleic acids symposium series, (15)(15), 89-92 (1984-01-01)
Greene, T.W. Wuts, P.G.M.
Protective Groups in Organic Synthesis (1991)

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