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Details

Stereochemistry ACHIRAL
Molecular Formula C7H7.Na
Molecular Weight 114.1202
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Benzylsodium

SMILES

[Na+].[CH2-]C1=CC=CC=C1

InChI

InChIKey=OWMHBKYAOYHOQK-UHFFFAOYSA-N
InChI=1S/C7H7.Na/c1-7-5-3-2-4-6-7;/h2-6H,1H2;/q-1;+1

HIDE SMILES / InChI

Molecular Formula C7H8
Molecular Weight 92.1384
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Toluene is a colorless, water-insoluble liquid with the smell associated with paint thinners. It is a mono-substituted benzene derivative, consisting of a CH3 group attached to a phenyl group. The major use of toluene is as a mixture added to gasoline to improve octane ratings. Toluene is also usedto produce benzene and as a solvent in paints, coatings, synthetic fragrances, adhesives, inks, and cleaningagents. Toluene is also used in the production of polymers used to make nylon, plastic soda bottles, andpolyurethanes and for pharmaceuticals, dyes, cosmetic nail products, and the synthesis of organicchemicals. The CNS is the primary target organ for toluene toxicity in both humans and animals for acute and chronicexposures. CNS dysfunction (which is often reversible) and narcosis have been frequently observed inhumans acutely exposed to low or moderate levels of toluene by inhalation; symptoms include fatigue,sleepiness, headaches, and nausea. CNS depression and death have occurred at higher levels of exposure. Toluene is used in veterinary medicine as a treatment for various parasites in dogs and cats. It is used for the removal of ascarids (Toxocara canis and Toxascaris leonina) and hookworms (Ancylostoma caninum and Uncinaria stenocephala) and as an aid in removing tapeworms (Taenia pisiformis, Dipylidium caninum, and Echinococcus granulosus) from dogs and cats.

Approval Year

PubMed

PubMed

TitleDatePubMed
Efficient charge separation in porphyrin-fullerene-ligand complexes.
2001
Environment and medication use influence olfactory abilities of older adults.
2001
A synthetic inhibitor of p53 protects neurons against death induced by ischemic and excitotoxic insults, and amyloid beta-peptide.
2001 Apr
Matrix metalloproteinase inhibitors cause cell cycle arrest and apoptosis in glomerular mesangial cells.
2001 Apr
Differential distribution of sialic acid in alpha2,3 and alpha2,6 linkages in the apical membrane of cultured epithelial cells and tissues.
2001 Apr
Rapid reduction of intracellular glutathione in human bronchial epithelial cells exposed to occupational levels of toluene diisocyanate.
2001 Apr
A stable organic free radical in anaerobic benzylsuccinate synthase of Azoarcus sp. strain T.
2001 Apr 20
Activity of different Candida antarctica lipase B formulations in organic solvents.
2001 Apr 20
Evaluation of natural attenuation rate at a gasoline spill site.
2001 Apr 20
Concise formation of 4-benzyl piperidines and related derivatives using a Suzuki protocol.
2001 Apr 6
Regio- and stereochemically controlled formation of hydroxamic acid containing anti- or syn-1,4-cycloalkenols from acylnitroso-derived Diels-Alder adducts.
2001 Apr 6
Suzuki reaction of vinyl triflates from six- and seven-membered N-alkoxycarbonyl lactams with boronic acids and esters.
2001 Apr 6
Enantioselective synthesis of (-)-wikstromol using a new approach via malic acid.
2001 Apr 6
Diverse profiles of specific IgE response to toluene diisocyanate (TDI)-human serum albumin conjugate in TDI-induced asthma patients.
2001 Feb
Formation of cleavage products by autoxidation of lycopene.
2001 Feb
Acetyl-coa: alcohol acetyltransferase activity and aroma formation in ripening melon fruits.
2001 Feb
Global and cognate regulators control the expression of the organic solvent efflux pumps TtgABC and TtgDEF of Pseudomonas putida.
2001 Feb
Health information in material safety data sheets for a chemical which causes asthma.
2001 Feb
A rapid method for peroxide value determination in edible oils based on flow analysis with Fourier transform infrared spectroscopic detection.
2001 Feb
Convenient synthesis of 4,6-di-O-benzyl-myo-inositol and myo-inositol 1,3,5-orthoesters.
2001 Feb 15
Titanium alkali metal nitrido complexes.
2001 Feb 2
Indoor and outdoor BTX levels in German cities.
2001 Feb 21
Determination of monobromobimane derivatives of phenylmercapturic and benzylmercapturic acids in urine by high-performance liquid chromatography and fluorimetry.
2001 Feb 25
Molecular characterization of the cDNA encoding an acidic isoform of PR-1 protein in rice.
2001 Feb 28
Selenoxides inhibit delta-aminolevulinic acid dehydratase.
2001 Feb 3
A capillary electrophoresis chip for the analysis of print and film photographic developing agents in commercial processing solutions using indirect fluorescence detection.
2001 Jan
Evaluation of porous ceramic as microbial carrier of biofilter to remove toluene vapor.
2001 Jan
Removal of toluene in gas streams by a fibrous-bed trickling filter.
2001 Jan
Application of high performance anion exchange chromatography to study invertase-catalysed hydrolysis of sucrose and formation of intermediate fructan products.
2001 Jan
BTEX catabolism interactions in a toluene-acclimatized biofilter.
2001 Jan
The first crystalline alkali metal salt of a benzenoid radical anion without a stabilizing substituent and of a related dimer: X-ray structures of the toluene radical anion and of the benzene radical anion dimer potassium-crown ether salts.
2001 Jan 10
Mixed dimer and mixed trimer complexes of nBuLi and a chiral lithium amide.
2001 Jan 19
Design and evaluation of a breath-analysis system for biological monitoring of volatile compound.
2001 Jan-Feb
Dermal absorption of neat liquid solvents on brief exposures in volunteers.
2001 Jan-Feb
Failure of GPI compounds to display neurotrophic activity in vitro and in vivo.
2001 Mar
5-Benzyl-5-phenyl[1,3]dithiolo[4,5-d]-[1,3]dithiole-2-thione.
2001 Mar
6,7-Bis(bromomethyl)-2,11,18,21,24-pentaoxatetracyclo.
2001 Mar
C-Isoprenylation of flavonoids enhances binding affinity toward P-glycoprotein and modulation of cancer cell chemoresistance.
2001 Mar 1
Reduction in glial immunity and neuropathology by a PAF antagonist and an MMP and TNFalpha inhibitor in SCID mice with HIV-1 encephalitis.
2001 Mar 1
Significance of nucleobase shape complementarity and hydrogen bonding in the formation and stability of the closed polymerase-DNA complex.
2001 Mar 13
Peptide transport by the multidrug resistance protein MRP1.
2001 Mar 15
The determination of draining lymph node cell cytokine mRNA levels in BALB/c mice following dermal sodium lauryl sulfate, dinitrofluorobenzene, and toluene diisocyanate exposure.
2001 Mar 15
Synthesis of biaryls via unusual deoxygenative dimerization of 1,4-epoxy-1,4-dihydroarenes catalyzed by palladium complexes.
2001 Mar 22
Bioactive chemical constituents from Alchornea laxiflora (benth) pax and hoffman.
2001 Mar 3
Determination of thiodyglycol in groundwater using solid-phase extraction followed by gas chromatography with mass spectrometric detection in the selected-ion mode.
2001 Mar 9
Stereocontrolled synthesis of acyclic 1,3-diols via condensation of tungsten-syn-pi-pentadienyl complexes with aldehydes. A new Prins reaction via s-trans-diene cationic intermediates.
2001 Mar 9
The role of delta-opioid receptor subtypes in neuropathic pain.
2001 Mar 9
Detection of catabolic genes in indigenous microbial consortia isolated from a diesel-contaminated soil.
2001 May
The essential HupB and HupN proteins of Pseudomonas putida provide redundant and nonspecific DNA-bending functions.
2001 May 18
Solvent vapour monitoring in work space by solid phase micro extraction.
2001 May 7
Substance Class Chemical
Created
by admin
on Sat Dec 16 12:39:21 GMT 2023
Edited
by admin
on Sat Dec 16 12:39:21 GMT 2023
Record UNII
FW9YL9W83J
Record Status Validated (UNII)
Record Version
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Name Type Language
Benzylsodium
Systematic Name English
Sodium phenylmethanide
Common Name English
Code System Code Type Description
FDA UNII
FW9YL9W83J
Created by admin on Sat Dec 16 12:39:21 GMT 2023 , Edited by admin on Sat Dec 16 12:39:21 GMT 2023
PRIMARY
PUBCHEM
11789171
Created by admin on Sat Dec 16 12:39:21 GMT 2023 , Edited by admin on Sat Dec 16 12:39:21 GMT 2023
PRIMARY
CAS
1121-53-5
Created by admin on Sat Dec 16 12:39:21 GMT 2023 , Edited by admin on Sat Dec 16 12:39:21 GMT 2023
PRIMARY
ECHA (EC/EINECS)
214-332-0
Created by admin on Sat Dec 16 12:39:21 GMT 2023 , Edited by admin on Sat Dec 16 12:39:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID30149911
Created by admin on Sat Dec 16 12:39:21 GMT 2023 , Edited by admin on Sat Dec 16 12:39:21 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE