ContaminantDB: 4-(Isopropylamino) Diphenylamine

Identification Taxonomy Biological Properties Physical Properties Toxicity Profile Spectra Concentrations Links References XML

Record Information

Version

1.0

Creation Date

2016-05-19 02:56:18 UTC

Update Date

2016-11-09 01:13:54 UTC

Accession Number

CHEM008992

Identification

Common Name

4-(Isopropylamino) Diphenylamine

Class

Small Molecule

Description

The N-substituted diamine that is 1,4-phenylenediamine substituted at one N with an isopropyl group and at the other with a phenyl group.

Contaminant Sources

HPV EPA Chemicals
OECD HPV Chemicals
STOFF IDENT Compounds
ToxCast & Tox21 Chemicals

Contaminant Type

Not Available

Chemical Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
-Isopropylaminodiphenylamine	ChEBI
4-(Isopropylamino)diphenylamine	ChEBI
4-Anilino-N-isopropylaniline	ChEBI
IPPD	ChEBI
N-(1-Methylethyl)-n'-phenyl-1,4-benzenediamine	ChEBI
N-Isopropyl-n'-phenyl-1,4-phenylenediamine	ChEBI
N-Isopropyl-N-phenyl-4-phenylenediamine	MeSH
N-Isopropyl-n'-phenyl-P-phenylenediamine	MeSH
N-Isopropyl-N-phenyl-4-phenylenediamine hydrochloride	MeSH
P-Isopropylaminodiphenylamine	MeSH
Phenylisopropyl-P-phenylenediamine	MeSH

Chemical Formula

C₁₅H₁₈N₂

Average Molecular Mass

226.323 g/mol

Monoisotopic Mass

226.147 g/mol

CAS Registry Number

101-72-4

IUPAC Name

N1-phenyl-N4-(propan-2-yl)benzene-1,4-diamine

Traditional Name

IPPD

SMILES

CC(C)NC1=CC=C(NC2=CC=CC=C2)C=C1

InChI Identifier

InChI=1S/C15H18N2/c1-12(2)16-14-8-10-15(11-9-14)17-13-6-4-3-5-7-13/h3-12,16-17H,1-2H3

InChI Key

OUBMGJOQLXMSNT-UHFFFAOYSA-N

Chemical Taxonomy

Description

belongs to the class of organic compounds known as phenylisopropylamines. These are organic aromatic compounds containing a 1-phenylpropan-2-amine moiety.

Kingdom

Organic compounds

Super Class

Organic nitrogen compounds

Class

Organonitrogen compounds

Sub Class

Amines

Direct Parent

Phenylisopropylamines

Alternative Parents

Substituents

Phenylisopropylamine
Aniline or substituted anilines
Secondary aliphatic/aromatic amine
Benzenoid
Monocyclic benzene moiety
Secondary amine
Organopnictogen compound
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

N-substituted diamine (CHEBI:63569 )

Biological Properties

Status

Detected and Not Quantified

Origin

Not Available

Cellular Locations

Not Available

Biofluid Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Applications

Not Available

Biological Roles

Not Available

Chemical Roles

Not Available

Physical Properties

State

Not Available

Appearance

Not Available

Experimental Properties

Property	Value
Melting Point	Not Available
Boiling Point	Not Available
Solubility	Not Available

Predicted Properties

Property	Value	Source
Water Solubility	0.048 g/L	ALOGPS
logP	4.22	ALOGPS
logP	3.66	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Basic)	6.42	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	24.06 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	73.91 m³·mol⁻¹	ChemAxon
Polarizability	27.06 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	1	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-004i-0390000000-f7d34d7addaeaead6699	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-017r-1930000000-3afd774a66097082c456	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-014i-3900000000-0c415d00b195ee533a5a	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-004i-0090000000-3b3af545907f788af555	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-004i-2290000000-2e4a57f0f44c4abc0515	Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-052f-9410000000-98d2f53e89c38817a5f9	Spectrum

Toxicity Profile

Route of Exposure

Not Available

Mechanism of Toxicity

Not Available

Metabolism

Not Available

Toxicity Values

Not Available

Lethal Dose

Not Available

Carcinogenicity (IARC Classification)

Not Available

Uses/Sources

Not Available

Minimum Risk Level

Not Available

Health Effects

Not Available

Symptoms

Not Available

Treatment

Not Available

Concentrations

Not Available

External Links

DrugBank ID

Not Available

HMDB ID

Not Available

FooDB ID

Not Available

Phenol Explorer ID

Not Available

KNApSAcK ID

Not Available

BiGG ID

Not Available

BioCyc ID

Not Available

METLIN ID

Not Available

PDB ID

Not Available

Wikipedia Link

Not Available

Chemspider ID

Not Available

ChEBI ID

63569

PubChem Compound ID

Not Available

Kegg Compound ID

Not Available

YMDB ID

Not Available

ECMDB ID

Not Available

References

Synthesis Reference

Not Available

MSDS

Not Available

General References

1. https://www.ncbi.nlm.nih.gov/pubmed/?term=19338586

2. https://www.ncbi.nlm.nih.gov/pubmed/?term=21616561

3. https://www.ncbi.nlm.nih.gov/pubmed/?term=7204095

4. https://www.ncbi.nlm.nih.gov/pubmed/?term=8156758

5. https://www.ncbi.nlm.nih.gov/pubmed/?term=8384542

6. https://www.ncbi.nlm.nih.gov/pubmed/?term=8462307

4-(Isopropylamino) Diphenylamine (CHEM008992)

Structure for CHEM008992: 4-(Isopropylamino) Diphenylamine