U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C12H12
Molecular Weight 156.2237
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,2-DIMETHYLNAPHTHALENE

SMILES

CC1=CC=C2C=CC=CC2=C1C

InChI

InChIKey=QNLZIZAQLLYXTC-UHFFFAOYSA-N
InChI=1S/C12H12/c1-9-7-8-11-5-3-4-6-12(11)10(9)2/h3-8H,1-2H3

HIDE SMILES / InChI

Molecular Formula C12H12
Molecular Weight 156.2237
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
A molecular and co-evolutionary context for grazer induced toxin production in Alexandrium tamarense.
2010-11-29
Lethal and sublethal effects of naphthalene and 1,2-dimethylnaphthalene on naupliar and adult stages of the marine cyclopoid copepod Oithona davisae.
2009-04
Pyrene fate affected by humic acid amendment in soil slurry systems.
2008-09-10
Predicting survival of grass shrimp (Palaemonetes pugio) exposed to naphthalene, fluorene, and dibenzothiophene.
2008-08
Dermal exposure to jet fuel suppresses delayed-type hypersensitivity: a critical role for aromatic hydrocarbons.
2007-12
Relaxation time, diffusion, and viscosity analysis of model asphalt systems using molecular simulation.
2007-11-21
Gene expression and target tissue dose in the rat epidermis after brief JP-8 and JP-8 aromatic and aliphatic component exposures.
2007-06
Electronic polarizability as a predictor of biodegradation rates of dimethylnaphthalenes. an ab initio and density functional theory study.
2007-03-01
Predicting survival of grass shrimp (Palaemonetes pugio) during ethylnaphthalene, dimethylnaphthalene, and phenanthrene exposures differing in concentration and duration.
2007-03
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Predictive three-dimensional quantitative structure-activity relationship of cytochrome P450 1A2 inhibitors.
2005-06-02
Effect of in vivo jet fuel exposure on subsequent in vitro dermal absorption of individual aromatic and aliphatic hydrocarbon fuel constituents.
2005-05-14
Comparative in vivo toxicity of topical JP-8 jet fuel and its individual hydrocarbon components: identification of tridecane and tetradecane as key constituents responsible for dermal irritation.
2005
Dose Related Absorption of JP-8 Jet Fuel Hydrocarbons Through Porcine Skin with Quantitative Structure Permeability Relationship Analysis.
2004
Chemical composition of the essential oils of two Chinese endemic Meconopsis species.
2003-07-23
The cytotoxicity of jet fuel aromatic hydrocarbons and dose-related interleukin-8 release from human epidermal keratinocytes.
2003-07
Rate constants for the gas-phase reactions of a series of alkylnaphthalenes with the nitrate radical.
2003-01-15
Reassessment of the hydrocarbons in Prince William Sound and the Gulf of Alaska: identifying the source using partial least-squares.
2002-06-01
Rate constants for the gas-phase reactions of a series of alkylnaphthalenes with the OH radical.
2002-05-01
Dansyl chloride derivatization of methamphetamine: a method with advantages for screening and analysis of methamphetamine in urine.
2002-03-13
Humic acid enhanced remediation of an emplaced diesel source in groundwater. 2. Numerical model development and application.
2002-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:39:36 GMT 2025
Edited
by admin
on Mon Mar 31 19:39:36 GMT 2025
Record UNII
23T7O135BD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-59832
Preferred Name English
1,2-DIMETHYLNAPHTHALENE
Systematic Name English
NAPHTHALENE, 1,2-DIMETHYL-
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 54002
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
Code System Code Type Description
ECHA (EC/EINECS)
209-364-7
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
EPA CompTox
DTXSID1058717
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
ECHA (EC/EINECS)
249-241-5
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
ALTERNATIVE
CAS
28804-88-8
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
GENERIC (FAMILY)
NSC
59832
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
PUBCHEM
11317
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
FDA UNII
23T7O135BD
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
CHEBI
34052
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY
CAS
573-98-8
Created by admin on Mon Mar 31 19:39:36 GMT 2025 , Edited by admin on Mon Mar 31 19:39:36 GMT 2025
PRIMARY