319937
N,N-Dimethylformamide
ACS reagent, ≥99.8%
Synonym(s):
DMF, NSC 5356
About This Item
Recommended Products
grade
ACS reagent
Quality Level
vapor density
2.5 (vs air)
vapor pressure
2.7 mmHg ( 20 °C)
Assay
≥99.8%
form
liquid
autoignition temp.
833 °F
expl. lim.
15.2 %
impurities
≤0.0005 meq/g Titr. acid
≤0.003 meq/g Titr. base
≤0.15% water
evapn. residue
≤0.005%
color
clear
APHA: ≤15
refractive index
n20/D 1.430 (lit.)
pH
7 (20 °C, 200 g/L)
bp
153 °C (lit.)
mp
−61 °C (lit.)
density
0.944 g/mL (lit.)
SMILES string
[H]C(=O)N(C)C
InChI
1S/C3H7NO/c1-4(2)3-5/h3H,1-2H3
InChI key
ZMXDDKWLCZADIW-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
Application
- A formylating agent for organometallic compounds.
- A reactant to prepare Vilsmeier reagent by reacting with phosphorus oxychloride.
- A reagent for amination of aryl chlorides in the presence of potassium t-butoxide.
- A reducing agent for metal salts to prepare metal colloids.
- A catalyst for the regioselective silylation of unprotected carbohydrates.
DMF can also be used in the following:
- DMF-Phosgene catalytic system is used to prepare alkyl halides from alcohols.
- DMF-POCl3 is used to convert acyclic and cyclic enolizable ketones to β-chloro-α, β-unsaturated aldehydes.
- DMF-POCl3 is used to synthesize quinoline-3-carbaldehydes from acylanilides.
- DMF-SOCl2 combination is used to dehydrate oximes to nitriles.
- DMF-Ag2O converts α-bromopropionamides to oxazolidinones.
- DMF is frequently used as a solvent in many chemical reactions, which require a high solvency power.
greener alternative product
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 3 - Repr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point(F)
135.5 °F - closed cup
Flash Point(C)
57.5 °C - closed cup
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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