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Methylacrylamide

Methylacrylamide structure

Methylacrylamide 

structure

Methylacrylamide Basic Attributes

85.106

85.10

214-700-0

6728C288M3

DTXSID9041449

2924199090

Characteristics

29.1

0.1

0.9872 g/cm3 @ Temp: 20 °C

102-106 °C

84 °C @ Press: 3.0 Torr

103.6±4.8 °C

1.4340 (estimate)

Safety Information

III

6.1(b)

2810

R20/21/22

23-26-36/37/39

P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, P501

H302

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.

Drug Information

N-methylacrylamide

Methylacrylamide Use and Manufacturing

Methods of Manufacturing

(C) Into a 1000 mL four-necked flask equipped with a stirrer, a thermometer, and a gas introduction line, 400 g of Meo-DEAA obtained in the step (b)6.8 g of potassium hydroxide and 0.4 g of TDA were added.Thereafter, a flask was equipped with a distillation column equipped with a packing material, a condenser and a distillation receiver, a trace nitrogen gas was flowed as a carrier, While stirring the reaction solution, the pot temperature was adjusted to 180 ° C. and the degree of vacuum was adjusted to 60 kPa, The pyrolysis reaction was carried out for 12 hours, 307 g (purity = 93percent, yield = 92percent) of crude N, N-diethylacrylamide (DEAA) was obtained from a water condenser.Further, the obtained crude DEAA was transferred to a distillation purification apparatus equipped with a 20 cm McMahon packing (size 6 mm) packed tower and purified by distillation under reduced pressure (60 ° C./0.13 kPa)As a colorless liquid, 258 g of high purity product DEAA (purity 99.8percent) was obtained. Examples 2 to 18 In Example 1, The starting materials, the catalyst, the solvent, the polymerization inhibitor and the reaction conditions of each step were changed as shown in Table 1, and synthesis was carried out in the same manner as in to obtain the respective target compound.The results are shown in Table 2.

2-Propenamide, N-methyl-: ACTIVE

Computed Properties

Molecular Weight:85.10
XLogP3:0.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:85.052763847
Monoisotopic Mass:85.052763847
Topological Polar Surface Area:29.1
Heavy Atom Count:6
Complexity:67.9
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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