Skip to Content
Merck
CN

73137

2,2-Dimethoxypropane

analytical standard

Synonym(s):

Acetone dimethyl acetal

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
(CH3)2C(OCH3)2
CAS Number:
77-76-9
Molecular Weight:
104.15
UNSPSC Code:
41116107
NACRES:
NA.02
PubChem Substance ID:
329764648
EC Number:
201-056-0
Beilstein/REAXYS Number:
635678
MDL number:
MFCD00008479

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

2,2-Dimethoxypropane, analytical standard

InChI

1S/C5H12O2/c1-5(2,6-3)7-4/h1-4H3

InChI key

HEWZVZIVELJPQZ-UHFFFAOYSA-N

SMILES string

COC(C)(C)OC

grade

analytical standard

vapor density

3.59 (vs air)

vapor pressure

60 mmHg ( 15.8 °C)

assay

≥99.4% (GC)

shelf life

limited shelf life, expiry date on the label

expl. lim.

31 %, 58 °F
6 %, 27 °F

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.378 (lit.)
n20/D 1.378

bp

79-81 °C
83 °C (lit.)

density

0.847 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

2,2-Dimethoxypropane may be used as an analytical standard for the determination of the analyte in biological samples by headspace gas chromatography-mass spectrometry (HS-GC/MS) technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

General description

2,2-Dimethoxypropane is an organic compound, which may be used as a protecting agent in the process of the synthesis of structurally related alkaloids like narciclasine and lycoricidine using phenylbromide as the starting material.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

14.0 °F - closed cup

flash_point_c

-10 °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
BCCN5537
BCCM3441
BCCK6894
BCCK7767
BCCG2060

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

Quantitative determination of n-propane, iso-butane, and n-butane by headspace GC-MS in intoxications by inhalation of lighter fluid
Bouche MPLA, et al.
Journal of Analytical Toxicology, 26(1), 35-42 (2002)
Total Synthesis of Lycoricidine and Narciclasine by Chemical Dearomatization of Bromobenzene
Southgate.HE, et al.
Angewandte Chemie (Weinheim an der Bergstrasse, Germany), 129(47), 15245-15248 (2017)
Akito Takeuchi et al.
Biomedical chromatography : BMC, 24(5), 465-471 (2009-08-19)
A method for routinely determination of dimethyl sulfoxide (DMSO) and dimethyl sulfone (DMSO(2)) in human urine was developed using gas chromatography-mass spectrometry. The urine sample was treated with 2,2-dimethoxypropane (DMP) and hydrochloric acid for efficient removal of water, which causes
R Dierichs et al.
Histochemistry, 74(2), 263-269 (1982-01-01)
Dehydration with 2,2-dimethoxypropane acidified with 1 n HCl in an 1:100 volume ratio has been found to be unsuitable for the preservation of cell membranes in single cell preparations. Reducing the HCl concentration to 0.1 or 0.01 n results in
H J Beckmann et al.
Histochemistry, 76(3), 407-412 (1982-01-01)
Dehydration with 2,2-dimethoxypropane acidified with either 1 N HCL or 0.05 N HCL in an 1:100 ratio has been found to extract various biologically active lipids. The effect is enhanced by an increased proton concentration and seems to occur only
View All Related Papers

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