Basic information Safety Supplier Related

Bis(4-amino-2-chloro-3,5-diethylphenyl)methane

Basic information Safety Supplier Related

Bis(4-amino-2-chloro-3,5-diethylphenyl)methane Basic information

Product Name:
Bis(4-amino-2-chloro-3,5-diethylphenyl)methane
Synonyms:
  • LONZACURE(R) M-CDEA-GS
  • 4,4'-Methylenebis-3-Chloro-2,6-Diethylaniline(MCDEA)
  • Bis(4-amino-2-chloro-3,5-diethylphenyl)methane
  • 4,4'-METHYLENEBIS(3-CHLORO-2,6-DIETHYLAN
  • MCDEA,Bis(4-amino-2-chloro-3,5-diethylphenyl)methane
  • LONZACURE(R) M-CDEA
  • Benzenamine, 4,4-methylenebis3-chloro-2,6-diethyl-
  • Bis-(4-amino-3-chloro-2,6-diethylphenyl)-methane
CAS:
106246-33-7
MF:
C21H28Cl2N2
MW:
379.37
EINECS:
402-130-7
Mol File:
106246-33-7.mol
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Bis(4-amino-2-chloro-3,5-diethylphenyl)methane Chemical Properties

Melting point:
88 °C
Boiling point:
506.4±45.0 °C(Predicted)
Density 
1.154±0.06 g/cm3(Predicted)
bulk density
610-650kg/m3
vapor pressure 
0Pa at 25℃
storage temp. 
Store below +30°C.
solubility 
17000 in mg/100g standard fat at 20 ℃
form 
powder to lump
pka
3.76±0.25(Predicted)
color 
White to Light yellow to Light orange
Water Solubility 
20μg/L at 20℃
InChI
InChI=1S/C21H28Cl2N2/c1-5-12-9-14(18(22)16(7-3)20(12)24)11-15-10-13(6-2)21(25)17(8-4)19(15)23/h9-10H,5-8,11,24-25H2,1-4H3
InChIKey
VIOMIGLBMQVNLY-UHFFFAOYSA-N
SMILES
C(C1=CC(CC)=C(N)C(CC)=C1Cl)C1=CC(CC)=C(N)C(CC)=C1Cl
LogP
6.5 at 20℃
CAS DataBase Reference
106246-33-7(CAS DataBase Reference)
EPA Substance Registry System
Benzenamine, 4,4'-methylenebis[3-chloro-2,6-diethyl- (106246-33-7)
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Safety Information

HS Code 
2921.59.1700
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Bis(4-amino-2-chloro-3,5-diethylphenyl)methane Usage And Synthesis

Chemical Properties

Crystalline Powder

Uses

LONZACURE(R) M-CDEA is an excellent chain extender for elastomeric polyurethanes (PU) and also a curing agent for epoxides (EP). It provides improved mechanical and dynamic properties which cannot be achieved with standard formulations.

Uses

LONZACURE(R) M-CDEA GS is the granulated version of LONZACURE(R) M-CDEA and therefore especially suitable for automatic feeding systems in production lines. It is an excellent chain extender for elastomeric polyurethanes (PU) and also.

Flammability and Explosibility

Not classified

Synthesis

13680-35-8

106246-33-7

The general procedure for the synthesis of 4,4'-methylenebis(2,6-diethylaniline) from 4,4'-methylenebis(3-chloro-2,6-diethylaniline) is as follows: 310 g (1 mol) of 4,4'-methylenebis(2,6-diethylaniline) (MDEA) was added to a three-necked flask fitted with a stirrer, thermometer and dropping funnel. At room temperature, 292.5 g (2.4 mol) of 30% hydrochloric acid solution was slowly added through the dropping funnel and stirred for 15 minutes until complete dissolution. Subsequently, 255.5 g (2.1 mol) of 30% hydrochloric acid solution was added, the reaction temperature was maintained at 45 °C and 262.3 g (2.7 mol) of 35% hydrogen peroxide solution was added slowly dropwise at this temperature and the dropwise process lasted for 2 hours. After completion of the dropwise addition, the reaction temperature was raised to 65°C and maintained for 1 hour. After completion of the reaction, the reaction mixture was cooled to below 10°C and left to stand for 10 hours. The solids and liquids were separated by pressurized filtration. The acidic mother liquor obtained from the separation was stored in an analytical grade vessel for subsequent synthesis of 4,4'-methylenebis(2,6-diethylaniline) (MDEA). The solid obtained by filtration was transferred to a three-necked flask and 200 g of water was added, followed by 280 g of 31% sodium hydroxide solution and stirred until neutralization was complete. After neutralization, the aqueous phase was separated by cooling, and the resulting solid was recrystallized from methanol using conventional methods to obtain white granular crystals, i.e., the target product 4,4'-methylenebis(3-chloro-2,6-diethylaniline). The purity of the product was analyzed by high performance liquid chromatography (HPLC) as 95.8%, in which 3,5-dichloro-4,4'-methylenebis(2,6-diethylaniline) was 0.5% and 3-chloro-4,4'-methylenebis(2,6-diethylaniline) was 1.3%. The above steps were repeated, the aqueous phase was separated after neutralization, the solid obtained was cooled and the fractions with boiling points of 245-250°C (fractions 7-8) were collected using a 30 x 0.5 magnetic ring distillation column. After distillation, the content of 4,4'-methylenebis(3-chloro-2,6-diethylaniline) was increased to 99.3% with a distillation yield of 95%, and this product can meet the demand of high-end polyurethane products.

References

[1] Patent: CN108329212, 2018, A. Location in patent: Paragraph 0040-0045
[2] Patent: CN105693526, 2016, A. Location in patent: Paragraph 0028; 0030; 0031

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