Documents
271012
N,N-Dimethylacetamide
anhydrous, 99.8%
Recommended Products
grade
anhydrous
Quality Level
vapor density
3 (vs air)
vapor pressure
2 mmHg ( 25 °C)
4 mmHg ( 38 °C)
Assay
99.8%
form
liquid
autoignition temp.
914 °F
expl. lim.
1.8 %, 100 °F
11.5 %, 160 °F
impurities
<0.005% water
evapn. residue
<0.001%
refractive index
n20/D 1.437 (lit.)
pH
4 (20 °C, 200 g/L)
bp
164.5-166 °C (lit.)
mp
−20 °C (lit.)
density
0.937 g/mL at 25 °C (lit.)
SMILES string
CN(C)C(C)=O
InChI
1S/C4H9NO/c1-4(6)5(2)3/h1-3H3
InChI key
FXHOOIRPVKKKFG-UHFFFAOYSA-N
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This Item | DX1545 | 17308 | DX1543 |
|---|---|---|---|
| vapor density 3 (vs air) | vapor density - | vapor density 3 (vs air) | vapor density - |
| vapor pressure 2 mmHg ( 25 °C), 4 mmHg ( 38 °C) | vapor pressure 1.76 hPa ( 20 °C) | vapor pressure 2 mmHg ( 25 °C), 4 mmHg ( 38 °C) | vapor pressure 1.76 hPa ( 20 °C) |
| assay 99.8% | assay ≥98% (GC) | assay ≥99.8% (GC) | assay ≥99.9% (GC) |
| form liquid | form liquid | form liquid | form liquid |
| autoignition temp. 914 °F | autoignition temp. - | autoignition temp. 914 °F | autoignition temp. - |
Application
- Palladium (II) acetate-butyldi-1-adamantylphosphine catalyzed arylation of 2-isobutylthiazole with chlorobenzene to form 5-phenyl-2-isobutylthiazole.
- Synthesis of β-, γ-, and δ-metallo ester intermediates that can react with acid chlorides to form γ-, δ-, and ε-keto esters.
- Synthesis of (R)-(-)-methyl 1,1′-binaphthyl-2,2′-diylphosphate that can be used as a precursor for preparing (R)-(+)-1,1′-binaphthalene-2,2′-diol.
Packaging
Other Notes
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Eye Irrit. 2 - Repr. 1B
Storage Class Code
6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 2
Flash Point(F)
147.2 °F - closed cup
Flash Point(C)
64 °C - closed cup
Personal Protective Equipment
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All of the preformed catalysts used in the kit are air and moisture stable complexes in their commercially available form. Once activated by base under the reaction conditions they become sensitive to air. To best enable scale-up success, the use of standard Schlenk technique is recommended.
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