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2162-74-5

2162-74-5 Structure

2162-74-5 Structure
IdentificationBack Directory
[Name]

Bis(2,6-diisopropylphenyl)carbodiimide
[CAS]

2162-74-5
[Synonyms]

carbod
Staboxol
staboxol1
HRstab-409
Stabilizer 7000
RARECHEM AQ A4 0133
Bis(2,6-diisopropylp
STABILIZER 7000 / 7000 F
VLOOKUP(C10,[1]Export!$D:$H,5,0)
(2,6-diisopropylphenyl)carbodiimide
BIS(2,6-DIISOPROPYLPHENYL)CARBODIIMIDE
bis(2,6-diisopropylphenyl)-carbodiimid
Bis(2,6-diisopropylphenyl)carbodiimide >
Bis(2,6-diisopropylphenyl)carbodiimide ,98%
N,N'-Bis(2,6-diisopropylphenyl)carbodiimide
2,2’,6,6’-Tetraisopropyldiphenylcarbodiimide
(2,6-diisopropylphenyl)carbodiimide/C25H34N2
N,N'-Methanediylidenebis(2,6-diisopropylaniline)
N,N'-bis[2,6-di(propan-2-yl)phenyl]methanediimine
N,N'-Bis[2,6-di(propan-2-yl)phenyl]methanediamine
N,N'-bis[2,6-di(propan-2-yl)phenyl]methanediimine
n,n’-methanetetraylbis[2,6-bis(1-methylethyl)-benzenamin
n,n’-methanetetraylbis(2,6-bis(1-methylethyl)-benzenamin
n,n’-methanetetraylbis(2,6-bis(1-methylethyl)benzenamine)
Benzenamine, N,N-methanetetraylbis2,6-bis(1-methylethyl)-
N,N’-methanetetraylbis[2,6-bis(1-methylethyl)-Benzenamine
(2,6-diisopropylphenyl)-[(2,6-diisopropylphenyl)iminomethylene]amine
[EINECS(EC#)]

218-487-5
[Molecular Formula]

C25H34N2
[MDL Number]

MFCD00082211
[MOL File]

2162-74-5.mol
[Molecular Weight]

362.55
Chemical PropertiesBack Directory
[Melting point ]

51 °C
[Boiling point ]

152-162 °C(Press: 0.05 Torr)
[density ]

0.95±0.1 g/cm3(Predicted)
[vapor pressure ]

0.006Pa at 20℃
[Fp ]

197℃
[storage temp. ]

Sealed in dry,2-8°C
[form ]

powder to lump
[color ]

White to Almost white
[Water Solubility ]

50μg/L at 20℃
[InChI]

InChI=1S/C25H34N2/c1-16(2)20-11-9-12-21(17(3)4)24(20)26-15-27-25-22(18(5)6)13-10-14-23(25)19(7)8/h9-14,16-19H,1-8H3
[InChIKey]

XLDBGFGREOMWSL-UHFFFAOYSA-N
[SMILES]

N(C1C(=CC=CC=1C(C)C)C(C)C)=C=NC1C(=CC=CC=1C(C)C)C(C)C
[LogP]

6.2 at 30℃
[CAS DataBase Reference]

2162-74-5
[EPA Substance Registry System]

Benzenamine, N,N'-methanetetraylbis[ 2,6-bis(1-methylethyl)-(2162-74-5)
Questions And AnswerBack Directory
[Uses]

N,N'-Di(2,6-diisopropylphenyl)carbodiimide is an anti-hydrolysis agent. Anti-hydrolysis agent K-1 is a sterically hindered aromatic carbodiimide anti-hydrolysis stabilizer. It reacts with the hydrolysis product carboxylic acid or water, preventing autocatalytic hydrolysis degradation and improving the service life of many polymers, especially enhancing their anti-hydrolysis and hydrolysis stability under harsh operating conditions such as high temperature, humidity, and acid/alkali environments. Its main applications include stabilizing polyester products, polyurethane products (such as PU systems, MDI prepolymers, TPU, adhesives), polyamide-nylon products, and hydrolyzable plastics such as EVA.
Hazard InformationBack Directory
[Chemical Properties]

White solid
[Hazard]

A poison by ingestion.
[Safety Profile]

A poison by ingestion,intraperitoneal, and inhalation. When heated todecomposition it emits toxic vapors of NOx.
[Synthesis]

Thiourea, N,N'-bis[2,6-bis(1-methylethyl)phenyl]-

25348-97-4

Bis(2,6-diisopropylphenyl)carbodiimide

2162-74-5

General procedure for the synthesis of N,N'-bis(2,6-diisopropylphenyl)carbodiimide from the compound (CAS: 25348-97-4): to a stirred DippN(H)C(S)N(H)Dipp (7.93 g, 20.0 mmol) and triethylamine (NEt3, 5.58 mL, 40.0 mmol) ethyl acetate (100 mL ) solution, iodine (I2, 5.58 g, 22.0 mmol) was added in batches over 30 min. The reaction mixture was stirred at room temperature for 2 h. Subsequent filtration gave a brown filtrate. The volatile components of the filtrate were removed by distillation under reduced pressure to give a brown solid. The solid was extracted with pentane (4 x 50 mL) and the extract was filtered through a short silica column. The brown filtrate obtained was added to activated copper powder (Cu, 3.00 g, 48.0 mmol). The mixture was stirred at room temperature for 16 h to form a black suspension. The suspension was filtered through silica to obtain a colorless filtrate. The volatile components in the filtrate were removed by distillation under reduced pressure and the solid obtained was dried under vacuum to give the target product N,N'-bis(2,6-diisopropylphenyl)carbodiimide as a colorless crystalline solid. Yield: 4.74 g (65%). The 1H NMR spectrum of the product was in agreement with the data reported by Cowley et al. [24]

[References]

[1] Synlett, 2009, # 4, p. 607 - 610
[2] New Journal of Chemistry, 2016, vol. 40, # 9, p. 7627 - 7636
[3] Dalton Transactions, 2008, # 33, p. 4419 - 4423
[4] Polyhedron, 2016, vol. 116, p. 64 - 75
[5] European Journal of Inorganic Chemistry, 2014, # 9, p. 1446 - 1453
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H301
[Precautionary statements ]

P264-P270-P301+P310+P330-P405-P501
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39-24/25
[RIDADR ]

2811
[RTECS ]

CY0887250
[TSCA ]

TSCA listed
[REACH Registrations]

Active
[HazardClass ]

6.1
[PackingGroup ]

III
[HS Code ]

29213000
[Toxicity]

LD50 orl-rat: 200 mg/kg NTIS** OTS0545280
Spectrum DetailBack Directory
[Spectrum Detail]

Bis(2,6-diisopropylphenyl)carbodiimide(2162-74-5)1HNMR
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