1,3-Benzenedicarboxamide, N,N'-bis(2,2,6,6-tetramethyl-4-piperidinyl)-

Base Information Edit

Chemical Name:1,3-Benzenedicarboxamide, N,N'-bis(2,2,6,6-tetramethyl-4-piperidinyl)-
CAS No.:42774-15-2
Deprecated CAS:212059-00-2,496934-97-5
Molecular Formula:C26H42N4O2
Molecular Weight:442.645
Hs Code.:
European Community (EC) Number:419-710-0
UNII:ZJD6FK539H
DSSTox Substance ID:DTXSID3068417
Nikkaji Number:J1.242.345D
Wikidata:Q72447035
Mol file:42774-15-2.mol

Synonyms:42774-15-2;N1,N3-Bis(2,2,6,6-tetramethylpiperidin-4-yl)isophthalamide;N,N'-BIS(2,2,6,6-TETRAMETHYL-4-PIPERIDINYL)-1,3-BENZENEDICARBOXAMIDE;1,3-Benzenedicarboxamide, N,N'-bis(2,2,6,6-tetramethyl-4-piperidinyl)-;N,N'-Bis(2,2,6,6-tetramethyl-4-piperidyl)isophthalamide;ZJD6FK539H;1-N,3-N-bis(2,2,6,6-tetramethylpiperidin-4-yl)benzene-1,3-dicarboxamide;C26H42N4O2;1,3-Benzenedicarboxamide, N1,N3-bis(2,2,6,6-tetramethyl-4-piperidinyl)-;EC 419-710-0;NYLOSTAB S-EED;UNII-ZJD6FK539H;SCHEMBL310763;DTXSID3068417;MFCD09751152;AKOS022173010;C26-H42-N4-O2;DS-7146;B6154;CS-0162605;FT-0660576;D83388;n,n'-bis(2,2,6,6-tetramethyl-4-piperidinyl)isophthalamide;1,3-Benzenedicarboxamide-N,n'-Bis-(2,2,6,6-Tetramethyl-4-Piperidinyl);N1,N3-bis(2,2,6,6-tetramethylpiperidin-4-yl)benzene-1,3-dicarboxamide

Suppliers and Price of 1,3-Benzenedicarboxamide, N,N'-bis(2,2,6,6-tetramethyl-4-piperidinyl)-

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
N1,N3-bis(2,2,6,6-Tetramethylpiperidin-4-yl)isophthalamide
1g
$ 85.00

Crysdot
N1,N3-Bis(2,2,6,6-tetramethylpiperidin-4-yl)isophthalamide 95+%
100g
$ 574.00

Chemenu
N1,N3-bis(2,2,6,6-tetramethylpiperidin-4-yl)isophthalamide 95%
100g
$ 542.00

Chemenu
N1,N3-bis(2,2,6,6-tetramethylpiperidin-4-yl)isophthalamide 95%
25g
$ 194.00

Chemenu
N1,N3-bis(2,2,6,6-tetramethylpiperidin-4-yl)isophthalamide 95%
10g
$ 102.00

Biosynth Carbosynth
N,N'-Bis(2,2,6,6-tetramethyl-4-piperidinyl)-1,3-benzenedicarboxamide
2 g
$ 766.00

Biosynth Carbosynth
N,N'-Bis(2,2,6,6-tetramethyl-4-piperidinyl)-1,3-benzenedicarboxamide
100 mg
$ 73.00

Biosynth Carbosynth
N,N'-Bis(2,2,6,6-tetramethyl-4-piperidinyl)-1,3-benzenedicarboxamide
250 mg
$ 145.00

Biosynth Carbosynth
N,N'-Bis(2,2,6,6-tetramethyl-4-piperidinyl)-1,3-benzenedicarboxamide
1 g
$ 440.00

Biosynth Carbosynth
N,N'-Bis(2,2,6,6-tetramethyl-4-piperidinyl)-1,3-benzenedicarboxamide
500 mg
$ 255.00

Total 73 raw suppliers

Chemical Property of 1,3-Benzenedicarboxamide, N,N'-bis(2,2,6,6-tetramethyl-4-piperidinyl)- Edit

Chemical Property:

Vapor Pressure:0Pa at 25℃
Boiling Point:605.1 °C at 760 mmHg
PKA:13.67±0.60(Predicted)
Flash Point:155.5 °C
PSA：82.26000
Density:1.09g/cm³
LogP:5.20400
Storage Temp.:under inert gas (nitrogen or Argon) at 2–8 °C
Solubility.:Chloroform (Slightly), Methanol (Slightly, Heated)
Water Solubility.:139mg/L at 30℃
XLogP3:3.2
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:442.33077660
Heavy Atom Count:32
Complexity:623

Purity/Quality:

99% ^*data from raw suppliers

N1,N3-bis(2,2,6,6-Tetramethylpiperidin-4-yl)isophthalamide ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn
Hazard Codes:Xn
Statements: 22-36
Safety Statements: 22-25-26

MSDS Files:

Useful:

Canonical SMILES:CC1(CC(CC(N1)(C)C)NC(=O)C2=CC(=CC=C2)C(=O)NC3CC(NC(C3)(C)C)(C)C)C

Technology Process of 1,3-Benzenedicarboxamide, N,N'-bis(2,2,6,6-tetramethyl-4-piperidinyl)-

There total 5 articles about 1,3-Benzenedicarboxamide, N,N'-bis(2,2,6,6-tetramethyl-4-piperidinyl)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 98.5%