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3323-53-3

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3323-53-3 Usage

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 3323-53-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3323-53:
(6*3)+(5*3)+(4*2)+(3*3)+(2*5)+(1*3)=63
63 % 10 = 3
So 3323-53-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H16N2.C6H10O4/c7-5-3-1-2-4-6-8;7-5(8)3-1-2-4-6(9)10/h1-8H2;1-4H2,(H,7,8)(H,9,10)/p-2

3323-53-3Synthetic route

1,6-Hexanediamine
124-09-4

1,6-Hexanediamine

Adipic acid
124-04-9

Adipic acid

hexanediyldiamine; adipate
3323-53-3

hexanediyldiamine; adipate

Conditions
ConditionsYield
With water
With methanol
With ethanol
hexanedinitrile
111-69-3

hexanedinitrile

hexanediyldiamine; adipate
3323-53-3

hexanediyldiamine; adipate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: sodium; NH3; ethanol
2: ethanol; water
View Scheme
Adipic acid
124-04-9

Adipic acid

N,N'-dimethyl-1,6-hexanediamine
13093-04-4

N,N'-dimethyl-1,6-hexanediamine

hexanediyldiamine; adipate
3323-53-3

hexanediyldiamine; adipate

Conditions
ConditionsYield
In ethanol
hexanediyldiamine; adipate
3323-53-3

hexanediyldiamine; adipate

55-amino-6,15,20,29,34,43,48-heptaoxo-7,14,21,28,35,42,49-heptaaza-pentapentacontanoic acid
10436-24-5

55-amino-6,15,20,29,34,43,48-heptaoxo-7,14,21,28,35,42,49-heptaaza-pentapentacontanoic acid

Conditions
ConditionsYield
With ethylene glycol
hexanediyldiamine; adipate
3323-53-3

hexanediyldiamine; adipate

Conditions
ConditionsYield
With ethylene glycol Neben anderen Verbindungen;
hexanediyldiamine; adipate
3323-53-3

hexanediyldiamine; adipate

ethylene glycol
107-21-1

ethylene glycol

N',N'''-bis-(6-amino-hexyl)-N,N''-hexanediyl-bis-adipamide
104397-76-4

N',N'''-bis-(6-amino-hexyl)-N,N''-hexanediyl-bis-adipamide

hexanediyldiamine; adipate
3323-53-3

hexanediyldiamine; adipate

6,15,20,29-tetraoxo-7,14,21,28-tetraaza-tetratriacontanedioic acid
119568-58-0

6,15,20,29-tetraoxo-7,14,21,28-tetraaza-tetratriacontanedioic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: ethylene glycol / Neben anderen Verbindungen
2: 160 - 180 °C
View Scheme

3323-53-3Downstream Products

3323-53-3Relevant articles and documents

Synthesis and characterization of a water-soluble nylon copolyamide

Bai, Yongping,Huang, Lei,Huang, Tong,Long, Jun,Zhou, Yongfeng

, p. 4171 - 4176 (2013/07/26)

A novel water-soluble copolyamide based on Nylon 66 was synthesized via solution-melt polycondensation of hexanedioic acid and sodium 5-sulfoisophthalate with 1,6-diaminohexane. The chemical structures of the products were ascertained by various spectroscopic techniques (FT-IR, Raman, and 1H NMR). The thermal properties of the polyamides under consideration were measured by TGA and DSC. According to the temperature dependence of FTIR spectra, it was found that the average strength of the intermolecular hydrogen bond of the water-soluble copolyamides becomes weak with increasing the temperature. It was found that the obtained random copolyamides could self-assemble into spherical micelles in aqueous solution with the size dependent on the hydrophilic fraction according to the DLS and TEM measurements.

Manufacture of a highly concentrated aqueous solution of a dicarboxylic acid diamine salt and a nylon precondensate

-

, (2008/06/13)

A process for the manufacture of a highly concentrated aqueous solution of a salt of a dicarboxylic acid and a diamine, as well as of a nylon precondensate, by reacting an alkanedicarboxylic acid of 6 to 12 carbon atoms and a diamine of the formula NH2 RNH2, where R is alkylene of 6 to 12 carbon atoms or is STR1 An aqueous solution, of lower concentration, of a salt of a dicarboxylic acid and a diamine, containing an appropriate dissolved excess of the particular dicarboxylic acid, is reacted with the particular diamine in the molten state, in an equivalent amount to the dissolved dicarboxylic acid, the reaction being carried out under superatmospheric pressure and the final reaction temperature being kept at from 140° to 210° C. The solution obtained is used for the manufacture of a nylon.

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