388246
Dimethylamine solution
2.0 M in methanol
Synonym(s):
N,N-Dimethylamine
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About This Item
Linear Formula:
(CH3)2NH
CAS Number:
Molecular Weight:
45.08
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
605257
Concentration:
1.90 -2.20 M (NaOH, titration), 2.0 M in methanol
Form:
liquid
form
liquid
Quality Level
concentration
1.90 -2.20 M (NaOH, titration), 2.0 M in methanol
density
0.775 g/mL at 25 °C
functional group
amine
SMILES string
CNC
InChI
1S/C2H7N/c1-3-2/h3H,1-2H3
InChI key
ROSDSFDQCJNGOL-UHFFFAOYSA-N
General description
Dimethylamine, a secondary amine, is used as a raw material for the production of many agrichemicals and pharmaceuticals. The solvents dimethylformamide (DMF) and dimethylacetamide (DMA) are derived from dimethylamine. It is also used as a precursor for the preparation of amido derivatives.
Application
Dimethylamine can be used as a precursor for the preparation of a number of chemical building blocks such as dimethyl(3-chloropropyl)amine , 2-chloro-N,N-dimethylethanimidamide , and 4, 6-dichloro-2-(dimethylamino)-1,3,5-triazine .
Packaging
The 25 mL Sure/Seal™ bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.
Legal Information
Sure/Seal is a trademark of Sigma-Aldrich Co. LLC
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Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 1 - STOT SE 3
target_organs
Eyes, Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
41.0 °F - closed cup
flash_point_c
5 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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4-Dimethylaminobutyraldehyde diethyl acetal
FENG R-l, et al.
JOURNAL-SHANDONG UNIVERSITY OF SCIENCE AND TECHNOLOGY NATURAL SCIENCE, 5 (2011)
Synthesis of 2-amino-4-imino-4, 5-dihydrothiazoles from N-sulfonyl-α -chloroamidines and thiourea
Abdelaal SM and Bauer L
Journal of Heterocyclic Chemistry, 25(6), 1849-1856 (1988)
Synthesis of 3-{4-[4-dimethylamino-6-(4-methyl-2-oxo-2H-chromen-7-yloxy)-[1, 3, 5] triazin-2-ylamino]-phenyl}-2-phenyl-5-(4-pyridin-2-yl-piperazin-1-ylmethyl)-thiazolidin-4-one and their biological evaluation
Patel D, et al.
Medicinal Chemistry Research, 21(10), 2926-2944 (2012)