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Details

Stereochemistry ACHIRAL
Molecular Formula C17H22N2
Molecular Weight 254.37
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MICHLER'S BASE

SMILES

CN(C)C1=CC=C(CC2=CC=C(C=C2)N(C)C)C=C1

InChI

InChIKey=JNRLEMMIVRBKJE-UHFFFAOYSA-N
InChI=1S/C17H22N2/c1-18(2)16-9-5-14(6-10-16)13-15-7-11-17(12-8-15)19(3)4/h5-12H,13H2,1-4H3

HIDE SMILES / InChI
Molecular Formula C17H22N2
Molecular Weight 254.37
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Electrochemical degradation of crystal violet with BDD electrodes: effect of electrochemical parameters and identification of organic by-products.
2010-09
Production of surfactin from Bacillus subtilis MZ-7 grown on pharmamedia commercial medium.
2007-06-05
Magnetic field effect on photoinduced electron transfer between dibenzo[a,c]phenazine and different amines in acetonitrile-water mixture.
2007-02-08
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
[A convenient method of isoflavonone synthesis].
2006-08-17
Exploring the extent of magnetic field effect on intermolecular photoinduced electron transfer in different organized assemblies.
2005-09-15
DNA fragmentation and DNA repair synthesis induced in rat and human thyroid cells by four rat thyroid carcinogens.
2005-03-01
4,4'-Methylenebis(N,N-dimethyl)benzenamine.
2004
Electrochiroptical response of 2,2'-(2,2-diarylethenyl)binaphthyl-type electron donors that undergo reversible C-C bond formation/breaking upon two-electron transfer.
2003-08-22
4,4'-Methylenebis(N,N-dimethyl)benzenamine.
2002
[Formation mechanism of 4,4-methylenebis(N,N-dimethylaniline) by the anodic oxidation of N,N-dimethylaniline].
2001-12
Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens.
2001-03
Promotive effect of 4,4'-methylenebis(N,N-dimethyl)benzenamine on N-bis(2-hydroxypropyl)nitrosamine-induced thyroid tumors in Wistar rats.
1988-06-30
Neoplastic response of F344 rats and B6C3F1 mice to the polymer and dyestuff intermediates 4,4'-methylenebis(N,N-dimethyl)-benzenamine, 4,4'-oxydianiline, and 4,4'-methylenedianiline.
1984-06
Morphology of the neoplasms of the thyroid gland in Fischer 344 rats treated with 4,4'-methylene-bis-(N,N-dimethyl)-benzenamine.
1980-10
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:11:31 GMT 2025
Edited
by admin
on Mon Mar 31 21:11:31 GMT 2025
Record UNII
L6SPP9K4WQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-36782
Preferred Name English
MICHLER'S BASE
MI  
Common Name English
P,P'-BIS(DIMETHYLAMINO)DIPHENYLMETHANE
Common Name English
ARNOLD'S BASE
Common Name English
ANILINE, 4,4'-METHYLENEBIS(N,N-DIMETHYL-
Systematic Name English
BENZENAMINE, 4,4'-METHYLENEBIS(N,N-DIMETHYL-
Systematic Name English
N,N,N',N-TETRAMETHYL-4,4'-METHYLENEDIANILINE
Common Name English
4,4'-BIS(DIMETHYLAMINO)DIPHENYLMETHANE
Common Name English
NSC-9029
Code English
REDUCED MICHLER'S KETONE
Common Name English
4,4'-METHYLENEBIS(N,N-DIMETHYL)BENZENAMINE
Common Name English
4,4'-METHYLENEBIS(N,N-DIMETHYLBENZENAMINE)
Systematic Name English
4,4'-METHYLENEBIS(N,N-DIMETHYLANILINE)
Systematic Name English
N,N,N',N'-TETRAMETHYL-4,4'-DIAMINODIPHENYLMETHANE
Common Name English
TETRABASE
Common Name English
4,4'-(DIMETHYLAMINO)DIPHENYLMETHANE
Common Name English
BIS(4-(N,N-DIMETHYLAMINO)PHENYL)METHANE
Systematic Name English
BIS(P-(DIMETHYLAMINO)PHENYL)METHANE
Common Name English
MICHLER'S METHANE
Common Name English
4,4'-TETRAMETHYLDIAMINODIPHENYLMETHANE
Common Name English
NSC-4892
Code English
MICHLER'S HYDRIDE
Common Name English
MICHLER'S BASE [MI]
Common Name English
4,4'-BIS(DIMETHYLAMINOPHENYL)METHANE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C45178
Created by admin on Mon Mar 31 21:11:31 GMT 2025 , Edited by admin on Mon Mar 31 21:11:31 GMT 2025
Code System Code Type Description
NCI_THESAURUS
C44402
Created by admin on Mon Mar 31 21:11:31 GMT 2025 , Edited by admin on Mon Mar 31 21:11:31 GMT 2025
PRIMARY
HSDB
2856
Created by admin on Mon Mar 31 21:11:31 GMT 2025 , Edited by admin on Mon Mar 31 21:11:31 GMT 2025
PRIMARY
MESH
C035472
Created by admin on Mon Mar 31 21:11:31 GMT 2025 , Edited by admin on Mon Mar 31 21:11:31 GMT 2025
PRIMARY
FDA UNII
L6SPP9K4WQ
Created by admin on Mon Mar 31 21:11:31 GMT 2025 , Edited by admin on Mon Mar 31 21:11:31 GMT 2025
PRIMARY
NSC
9029
Created by admin on Mon Mar 31 21:11:31 GMT 2025 , Edited by admin on Mon Mar 31 21:11:31 GMT 2025
PRIMARY
NSC
4892
Created by admin on Mon Mar 31 21:11:31 GMT 2025 , Edited by admin on Mon Mar 31 21:11:31 GMT 2025
PRIMARY
PUBCHEM
7567
Created by admin on Mon Mar 31 21:11:31 GMT 2025 , Edited by admin on Mon Mar 31 21:11:31 GMT 2025
PRIMARY
EPA CompTox
DTXSID5020869
Created by admin on Mon Mar 31 21:11:31 GMT 2025 , Edited by admin on Mon Mar 31 21:11:31 GMT 2025
PRIMARY
MERCK INDEX
m7525
Created by admin on Mon Mar 31 21:11:31 GMT 2025 , Edited by admin on Mon Mar 31 21:11:31 GMT 2025
PRIMARY Merck Index
CAS
101-61-1
Created by admin on Mon Mar 31 21:11:31 GMT 2025 , Edited by admin on Mon Mar 31 21:11:31 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-959-2
Created by admin on Mon Mar 31 21:11:31 GMT 2025 , Edited by admin on Mon Mar 31 21:11:31 GMT 2025
PRIMARY
SMS_ID
300000053732
Created by admin on Mon Mar 31 21:11:31 GMT 2025 , Edited by admin on Mon Mar 31 21:11:31 GMT 2025
PRIMARY
NSC
36782
Created by admin on Mon Mar 31 21:11:31 GMT 2025 , Edited by admin on Mon Mar 31 21:11:31 GMT 2025
PRIMARY
NIH
NCATS
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