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05937

Sigma-Aldrich

N,N-Dimethylallylamine

for protein sequence analysis

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Synonym(s):
3-Dimethylamino-1-propene, N-Allyl-dimethylamin, DMAA
Linear Formula:
CH2=CHCH2N(CH3)2
CAS Number:
2155-94-4
Molecular Weight:
85.15
Beilstein:
1734044
EC Number:
218-458-7
MDL number:
MFCD00038234
PubChem Substance ID:
329748185
NACRES:
NA.26

grade

for protein sequence analysis

density

0.719 g/mL at 20 °C (lit.)

SMILES string

CN(C)CC=C

InChI

1S/C5H11N/c1-4-5-6(2)3/h4H,1,5H2,2-3H3

InChI key

GBCKRQRXNXQQPW-UHFFFAOYSA-N

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Signal Word

Danger

Hazard Statements

H225 - H314 - H332

Hazard Classifications

Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

-4.0 °F - closed cup

Flash Point(C)

-20 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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G Braunitzer et al.
Biological chemistry Hoppe-Seyler, 368(3), 195-198 (1987-03-01)
The currently used base for gas-phase sequencing, trimethylamine, can be substituted by more hydrophobic tertiary amines without any problems. We used mainly N,N-dimethylallylamine and 3-(dimethylamino)propyne, both as aqueous solutions at constant temperature (40 degrees C). The advantages of these bases
František Bílek et al.
Colloids and surfaces. B, Biointerfaces, 102, 842-848 (2012-10-30)
Three monomers (allylamine, N-allylmethylamine and N,N-dimethylallylamine) were used for grafting onto air plasma activated LDPE surface. Antibacterial agent triclosan was anchored on such substrates. Influence of graft type on the antibacterial properties was determined. Increase of antibacterial activity and amount

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