Anthracene is a solid polycyclic aromatic hydrocarbon (PAH) of formula C 14 H 10, consisting of three fused benzene rings. It is a component of coal tar.Anthracene is used in the production of the red dye alizarin and other dyes. Anthracene is colorless but exhibits a blue (400-500 nm peak) fluorescence under ultraviolet radiation Anthracene is not currently considered a toxic substance. Phenanthrene is an isomer of anthracene and, as a result, many of the physical properties of the two are very similar. The major differences between anthracene and phenanthrene lie in the melting point and the properties directly related to solubility (Table 13.2). Phenanthrene is. Anthracene is a solid polycyclic aromatic hydrocarbon (PAH) consisting of three fused benzene rings. It is a component of coal-tar and the US Occupational Health and Safety Administration classifies it as noncarcinogenic. Anthracene is used in the production of the red dye alizarin and other dyes. Anthracene is colorless but exhibits a blue.

Anthracene - Wikipedi

Anthracene derivatives are used in a number of applications. 1-hydroxyanthracene and 2-hydroxyanthracene are hydroxylated derivatives of phenol and naphthols, and hydroxyanthracene (also known as anthrol and anthracenol) is pharmacologically active. 9,10-dihydroxyanthracene is an example of anthracene with several hydroxyl groups Anthracene (sat. sol. in toluene) 120-12-7: Liquid >480 >480 >480 > indicates greater than. A blank cell indicates the fabric has not been tested. The fabric may or may not offer barrier. Special Warnings from DuPont

Anthracene is a solid polycyclic aromatic hydrocarbon (PAH) of formula C 14 H 10, consisting of three fused benzene rings. It is a component of coal tar. Anthracene is used in the production of the red dye alizarin and other dyes L'anthracène est un composé chimique de formule C 14 H 10 synthétisé pour la première fois par Richard Anschütz.C'est un hydrocarbure aromatique polycyclique composé de trois noyaux benzèniques fusionnés en alignement.On l'obtient à partir du goudron.Il est utilisé pour la production industrielle d'alizarine, un pigment rouge naturel d'origine végétale, ainsi que dans les. アントラセン(anthracene)は、分子式 C 14 H 10 、分子量 178.23 の有機化合物の一種で、ベンゼン環が3個縮合したアセン系多環芳香族炭化水素。 融点は 218 ℃、沸点は 342 ℃ で、昇華性がある。 CAS登録番号は [120-12-7]。1832年、ジャン=バティスト・デュマによって発見された

蒽 ( ㄣ ) 舊稱荌( Anthracene ),俗稱綠油腦,一種稠環芳香烴,分子式C 14 H 10 ,分子量178.22。無色稜柱狀晶體,有藍紫色螢光,有昇華性,有毒。不溶於水,微溶於乙醇,溶於乙醚、苯、甲苯、氯仿、丙酮、四氯化碳。 蒽與菲為同分異構物。 易氯化 This optical absorption measurement of Anthracene were made by R.-C. A. Fuh on 06-26-1995 using a Cary 3. The absorption values were collected using a spectral bandwidth of 1.0 nm, a signal averaging time of 0.133 sec, a data interval of 0.25 nm, and a scan rate of 112.5 nm/min Anthracene has been shown to be soluble in a variety of binary and ternary mixtures of cyclohexanone, ethyl acetate, and methanol 1,2. Uses: Anthracene is an aromatic hydrocarbonwith three fused rings, and is obtained by the distillationof crude oils. The main useis in the manufacture of dyes.It is an important source of dyestuffs. Use

L'antracene è un composto idrocarburico policiclico aromatico (IPA) solido costituito da tre anelli benzenici condensati e possiede struttura lineare. L'antracene è utilizzato nell'industria dei coloranti per la sintesi del colorante Rosso d'alizarina.Era utilizzato anche come conservante nell'industria del legname, grazie alle sue proprietà insetticide Anthracene-d10, 98 atom % D. BAA71906. Anthracene-d10, analytical standard. MFCD00001241. AKOS015903833. Anthracene D10 10 microg/mL in Cyclohexane. Anthracene D10 100 microg/mL in Cyclohexane. D99665. ANTHRACENE D10 inverted exclamation markY98% Anthracene-1,2,3,4,5,6,7,8,9,10-d10. J-010779. Anthracene D10 2000 microg/mL in Methyl-tert-butyl ethe Anthracene derivatives are useful in preparing stable blue-emitting organic electroluminescence devices. It is oxidized to anthracene cis-1,2-dihydrodiol by Mycobacterium sp. strain PYR-12. It forms bis-adducts by [4+2]-cycloaddition reaction with [5,6]-fullerene C 60 anthracene is included in this fact sheet when available. What is anthracene used for? Most of the PAHs are used to conduct research. Like most PAHs, anthracene is used to make dyes, plastics and pesticides. It has been used to make smoke screens and scintillation counter crystals. A scintillation counter is used to detect or count the numbe Anthracene Revision Date 24-Dec-2021 Method - No information available Autoignition Temperature 540 °C / 1004 °F Explosion Limits Upper No data available Lower 0.6 vol % Sensitivity to Mechanical ImpactNo information available Sensitivity to Static DischargeNo information available Specific Hazards Arising from the Chemica

Anthracene certified reference material, TraceCERT®; CAS Number: 120-12-7; EC Number: 204-371-1; Synonyms: Anthraxcene,Paranaphthalene; find Supelco-07671 MSDS, related peer-reviewed papers, technical documents, similar products & more at Sigma-Aldric Anthracene has been shown to be soluble in a variety of binary and ternary mixtures of cyclohexanone, ethyl acetate, and methanol 1,2. Uses Anthracene is an aromatic hydrocarbonwith three fused rings, and is obtained by the distillationof crude oils. The main useis in the manufacture of dyes.It is an important source of dyestuffs. Use DRC-18-170856-11673B Version N°3.2 décembre 2019 Page 1 sur 48 INERIS - Fiche de données toxicologiques et environnementales des substances chimiques ANTHRACÈNE

Anthracene - an overview ScienceDirect Topic

  1. Anthracene, 0.5 mg/mL in Acetonitrile Anthracene, 1000 ug/mL in Acetone アントラセン (50μg/mL トルエン溶液) Anthracene, 100 ug/mL in Methanol Anthracene, 0.2 mg/mL in Methanol Anthracene, 1000 ug/mL in Methano
  2. Anthracene Zone Refined (number of passes:30) 製品コード. A0405. CAS RN. 120-12-7. 純度(試験方法). >99.5% (GC) 詳細を見る
  3. 정보상자 각주. 안트라센 (Anthracene)은 벤젠 고리가 직선으로 3개 있는 모양의 분자를 가진 무색 결정으로 분자량은 178.2, 녹는점은 218°C, 끓는점은 340°C이며, 비중은 1.25 (20°C)이다. 분자식은 C 14 H 10 로 쓴다. 페난트렌 과는 이성질체이다
  4. Anthracene is one of the smaller polynuclear aromatic hydrocarbons. (The only smaller one is naphthalene.) It was isolated from coal tar in 1832 by pioneering French chemists Jean-Baptiste Dumas and Auguste Laurent. Anthracene can be synthesized by the Elbs reaction, in which o -tolyl phenyl ketone is dehydrated at 400-450 ºC
  5. Anthracène. Nom anglais dans le règlement (si applicable) : Anthracene. CAS : 120-12-7. Substance non réglementée

Anthracene is a polycyclic aromatic hydrocarbon that has three benzene rings fused together. Sarah breaks it down very simply: polycyclic means more than one ring, aromatic means the molecule has. 「アントラセン」。富士フイルム和光純薬株式会社は、試験研究用試薬・抗体の製造販売および各種受託サービスを行っています。先端技術の研究から、ライフサイエンス関連、有機合成用や環境測定用試薬まで、幅広い分野で多種多様なニーズに応えています anthracene: ChEBI ID CHEBI:35298: Definition An ortho-fused tricyclic hydrocarbon comprising three fused benzene rings. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:34538, CHEBI:40737, CHEBI:29862. Anthracene-D10-Other names: Anthracin; Green Oil; Paranaphthalene; Tetra Olive N2G; Anthracene oil; p-Naphthalene; Anthracen; Coal tar pitch volatiles:anthracene; Sterilite hop defoliant Permanent link for this species. Use this link for bookmarking this species for future reference. Information on this page: Gas phase thermochemistry dat

Anthracene. Formula. C 14 H 10. Anthracene is used as an intermediate compound for the manufacturing of dyes and polyradicals used to make resins. It may also be used as a diluent for wood protection products, an insecticide, or a fungicide. Furthermore, anthracene is an organic cristallized photoconductor used in electrophotography Anthracene-D10-Other names: Anthracin; Green Oil; Paranaphthalene; Tetra Olive N2G; Anthracene oil; p-Naphthalene; Anthracen; Coal tar pitch volatiles:anthracene; Sterilite hop defoliant Permanent link for this species. Use this link for bookmarking this species for future reference. Information on this page: Mass spectrum (electron ionization Anthracene. Anthracene is a solid polycyclic aromatic hydrocarbon consisting of three fused benzene rings derived from coal-tar. Anthracene is used in the artificial production of the red dye alizarin. It is also used in wood preservatives, insecticides, and coating materials. Anthracene is colorless but exhibits a blue (400-500 nm peak. PubMed: In vitro interaction of 7,12-dimethylbenz [a]anthracene and its biliary metabolites with dietary fiber. PubMed: Inhibition of neoplasia by minor dietary constituents. PubMed: Effect of food restriction, dehydroepiandrosterone, or obesity on the binding of 3H-7,12-dimethylbenz (a)anthracene to mouse skin DNA

  1. Anthracene 1. Anthracene (Anthraquinone)Anthracene (Anthraquinone) GlycosidesGlycosides Anthracene glycosides are oxygenated derivatives of pharmacologicalAnthracene glycosides are oxygenated derivatives of pharmacological importance that are used as laxatives or cathartics, anti-inflammatory,importance that are used as laxatives or cathartics, anti-inflammatory, antibacterial, antifungal and.
  2. anthracene, a tricyclic aromatic hydrocarbon found in coal tar and used as a starting material for the manufacture of dyestuffs and in scintillation counters. Crude anthracene crystallizes from a high-boiling coal-tar fraction. It is purified by recrystallization and sublimation. Oxidation yield
  3. آخر تعديل لهذه الصفحة كان يوم 19 يونيو 2020، الساعة 08:09. النصوص مُرخّصة برخصة المُشاع الإبداعي: النسبة-الترخيص بالمثل.قد تنطبق بنود أخرى أيضًا
  4. The 14π-electron system of anthracene has been merged with the unsaturated Z-1,2-difurylethene to form a macrocycle(s) with the retained local conjugation of all incorporated subunits that were substantially modulated with a redox activation, opening a global delocalization involving all integrated aromatics. In addition, the edge modulation of acene via the attachment of a specific isomer of.
  5. 11-Azido-9,10-dihydro-9,10-phosphanoanthracene (N3PA) has been demonstrated recently as a transfer reagent for molecular phosphorus mononitride (PN) because it easily dissociates at room temperature into dinitrogen (N2), PN, and anthracene (A). Here we report further reactivity studies of the N3PA molecule including strain-promoted 1,3-dipolar cycloaddition with cyclooctyne and Staudinger-type.

Anthracene - Meaning, Reactions, Preparation and Use

Anthracene with a number of hydroxyl groups is 9,10-dihydroxyanthracene. The production of anthracene occurs in combustion processes, as is the case with many other polycyclic aromatic hydrocarbons. Smoke from tobacco products and combustion materials in food are the primary sources of exposure for humans The oxidation of anthracene. Chromium(VI) is the typical oxidant. The Friedel-Crafts reaction of benzene and phthalic anhydride in presence of AlCl 3. o-Benzoylbenzoic acid is an intermediate. This reaction is useful for producing substituted anthraquinones. The Diels-Alder reaction of naphthoquinone and butadiene followed by oxidative. Triplet anthracene then engages in concerted proton coupled electron transfer with the ground state iridium hydride promoting weak C-H bond formation. Identification of a photoinduced catalytic deactivation pathway and associated inverse deuterium KIE support deleterious C-H reductive coupling followed by haptotropic rearrangement anthracene 377 9,800 9-methylanthracene 387 10,200 • Alkyl substituents shift the 0-0 band of the parent aromatic a few nanometers to the red, and increase the molar absorptivity a small amount • Multiple substituents will increase the shift by smaller increments • The vibronic pattern in the spectrum will change because of th La dernière modification de cette page a été faite le 9 janvier 2022 à 14:22. Droit d'auteur: les textes sont disponibles sous licence Creative Commons attribution, partage dans les mêmes conditions; d'autres conditions peuvent s'appliquer.Voyez les conditions d'utilisation pour plus de détails, ainsi que les crédits graphiques.En cas de réutilisation des textes de cette page.


  1. o anthracene;Coal tar pitch volatiles:anthracene;EC 204-371-1;Green oil;NSC 7958;Sterilite hop defoliant;Tetra olive N2G.. Créé le: 07/11/200
  2. The study of organic scintillators has a long history 18.Commonly these scintillators are highly efficient fluorescent molecules, typified by anthracene, which has a PLQY as high as 80% 22,23.
  3. Anthracene as a type of PAHs is widely distributed in the environments due to many anthropogenic activities, like oil refining and the petro-chemical industry . Exposure to high doses of anthracene has toxic effects on skin and tissues . Anthracene has toxic effects on the growth of some eukaryotic microorganisms

Anthracene Registration dossier Other identifiers 120-12-7 EC Inventory, C&L Inventory, Candidate List, Registration dossier, Pre-Registration process, Water Framework Directive, Annex X - Priority Substances, Construction Product Regulation - Annex I (3) - Hazardous Substances, Construction Product Regulation - Art. 6(5) - SDS and Declaration. An organogel system can control the stereochemical course of anthracene photodimerization. Chem. Commun. 16, 2100-2102 (2009). Google Scholar 40. Ishida, Y. et al. Two-component liquid crystals.

Anthracene C14H10 ChemSpide

  1. Anthracene was observed to readily penetrate the skin in both experiments and the total amounts absorbed in vivo and in vivo were seen to gradually coalesce over time. Within six days after.
  2. Anthracene is a colorless to pale yellow, sand-like material with a bluish fluorescence. It is used in dyestuffs, insecticides and wood preservatives. REASON FOR CITATION * Anthracene is on the Hazardous Substance List because it is regulated by OSHA and cited by ACGIH, DOT, NIOSH, DEP, HHAG, NFPA and EPA. * Definitions are provided on page 5
  3. anthracene: ChEBI ID CHEBI:35298: Definition An ortho-fused tricyclic hydrocarbon comprising three fused benzene rings. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:34538, CHEBI:40737, CHEBI:29862.
  4. The recombinant protein Baa was overexpressed in E. coli BL21 (DE3). Further investigations on the recombinant protein Baa in E. coli demonstrated that it was able to oxidize anthracene and benz [a]anthracene, resulting in 9,10-dihydroxyanthracene and 7, 12-dihydroxybenz[a]anthracene as metabolites, respectively
  5. 20 Anthracene oil, anthracene paste, anthracene fraction アントラセン油、アントラセンペースト、アントラセン留分 295-275-9 91995-15-2 21 Anthracene oil アントラセン油 292-602-7 90640-80-5 22 Pitch, coal tar, high temp. ピッチ、コールタール、高温留分 266-028-2 65996-93-
  6. Consequently, the treatment of anthracene additive enables the power conversion efficiency (PCE) of PM6:Y6-based devices to 17.02%, which is a significant improvement with regard to the PCE of 15.60% for the reference device using conventional treatments
  7. anthracene glycosides Anthracene glycosides are chiefly found in dicot plants but to some extent it is also found in monocot and lower plants. It consists of glycosides formed from aglycone moi-eties like anthraquinones, anthranols, anthrones or dimers of anthrones or their derivatives
Anthracene - CAMEO

Boronic acid based anthracene dyes were designed, synthesized, and immobilized to solid phase, creating a continuous glucose sensor. Glucose sensitivities of dyes can decrease drastically after immobilization, therefore how to immobilize a dye to solid phase without changing the dye property is a key issue in developing the sensor Benz [a]anthracene. The 'Substance identity' section is calculated from substance identification information from all ECHA databases. The substance identifiers displayed in the InfoCard are the best available substance name, EC number, CAS number and/or the molecular and structural formulas. Some substance identifiers may have been claimed. The analysis results showed a decrease in the concentration of anthracene (21.89%) and pyrene (7.71%), equivalent to a ratio of 3:1, followed by a decrease in the abundance of anthracene (60.30%) and pyrene (27.52%), equivalent to a ratio of 2:1

Define anthracene. anthracene synonyms, anthracene pronunciation, anthracene translation, English dictionary definition of anthracene. n. A crystalline aromatic hydrocarbon, C14H10, extracted from coal tar and used in the manufacture of dyes and organic chemicals. American Heritage®.. Anthracene definition, a colorless, crystalline powder, C14H12, obtained from coal tar and having a violet fluorescence: used chiefly as a source of anthraquinone and alizarin, and in the process of measuring radioactive materials. See more Exosomes carry cellular proteins and contain molecules that can be potential biomarkers of diseases. This study used a Syrian golden hamster model of 7,12-dimethylbenz[a]anthracene (DMBA)-induced oral squamous cell carcinoma with radiation therapy to exclude the confounding factors that may affect outcomes in clinical studies, and re-examine the role of exosomes during tumorigenesis. We used. Media in category Anthracene. The following 51 files are in this category, out of 51 total. Anthraceen.PNG 954 × 638; 49 KB. Anthraceen2.png 235 × 82; 2 KB. Anthracen Oxygen Diels Alder Reaction.jpg 488 × 133; 14 KB. Anthracen-Dimerisierung.svg 512 × 104; 23 KB. Anthracen.svg 208 × 81; 5 KB

BENZ [A]ANTHRACENE†. tetraphene; 1,2-benzanthracene; benzanthrene; benzanthracene; benzo [a]anthracene. Colorless leaflets or plates or coarse gold powder with a greenish-yellow fluorescence. OSHA staff, please contact the SLTC before sampling (801) 233-4900. * All sampling instructions above are recommended guidelines for OSHA Compliance. Anthracene-based bipolar deep-blue emitters for efficient white OLEDs with ultra-high stabilities of emission color and efficiency† Xiangyu Zhu , a Yinghao Li , a Zilong Wu , a Chengwei Lin , a Dongge Ma , a Zujin Zhao * a and Ben Zhong Tang ab ANTHRACENE (from the Greek ἄνθραξ, coal), C 14 H 10, a hydrocarbon obtained from the fraction of the coal-tar distillate boiling between 270° and 400° C. This high boiling fraction is allowed to stand for some days, when it partially solidifies. It is then separated in a centrifugal machine, the low melting-point impurities are removed.

Anthracene is insoluble in water but is quite soluble in carbon disulfide and somewhat soluble in ethanol, methanol, benzene, chloroform, and other organic solvents. It is readily oxidized to form anthraquinone, the parent compound of the alizarin alizari Definition of anthracene in the Definitions.net dictionary. Meaning of anthracene. What does anthracene mean? Information and translations of anthracene in the most comprehensive dictionary definitions resource on the web Anthracene and Groundwater Anthracene Anthracene belongs to a class of compounds known as polycyclic aromatic hydrocarbons (PAHs). Anthracene naturally occurs as a component of fossil fuels (i.e. coal tar, oil, and gas) and is formed during incomplete combustion and processing of coal, oil, gas, and plant materials such as wood Anthracene-based π-congested cyclic dimer and tetramer were obtained using Ni(cod) 2. These cyclic π-clusters exhibit narrow HOMO-LUMO gaps, reflecting the face-to-face distance between the anthracene units. This π-congestion endows the cyclic anthracene dimer with multi-stimuli responsiveness such as photoisomerization and thermal. 120-12-7 - MWPLVEDNUUSJAV-UHFFFAOYSA-N - Anthracene - Similar structures search, synonyms, formulas, resource links, and other chemical information

7,12-ジメチルベンズ[a]アントラセン(7,12-dimethylbenz[a]anthracene)は、強い臓器特異的な発がん性物質である 。 7,12-ジメチルベンズ[α]アントラセンまたはDMBAとしても知られ、がん研究に広く用いられている。DMBAは必須な突然変異種として製造され、発がんイニシエーターとして供給されている an·thra·cene. 1. A hydrocarbon obtained from coal tar; it oxidizes to anthraquinone, which is converted to alizarin dyes. Synonym (s): anthracin. 2. A compound containing anthracene (1) as a part of its structure The assemblies can exhibit tunable fluorescence emission after undergoing a photoreaction of the anthracene unit in BPA. It is interesting that CB[8] can bind two bromophenylpyridinium units to form a green phosphorescent switch. Notably, the RTP of the assemblies can be reversibly switched on/off by UV irradiation or heating through a tunable. Anthracene is used in the production of the red dyealizarin and other dyes. Soluble in alcohol, methanol (1.8 g/100 g), hexane (0.37 g/100 g). Insoluble in water. Store in cool, dry conditions in well sealed containers. keep container tightly closed. Store away from strong oxidizing agents

Anthracene oil is a crop dessicant. It has a low aqueous solubility, non-mobile and is non-volatile. It is moderately persistent in most soil systems but not expected to be persistent in aqueous systems. Anthracene oil is moderately toxic to mammals but there is some concern regarding its potential to bioaccumulate Anthracene / Anthraquinone Glycosides | PharmD| Pharmacognos الويكيات الأخرى التالية تستخدم هذا الملف: الاستخدام في de.wikipedia.org Anthracen; Polycyclische aromatische Kohlenwasserstoff Anthracene exhibits an oxidation potential very similar to the one of pyrene (0.886 V and 0.893 V vs. Ferrocenium/Ferrocene couple, respectively, according to Davis and Fry, Supporting Information of ref. [25]) that makes it a non-activated PAH which cannot be oxidized in solution, using FeCl 3 or DDQ, in the presence of a Lewis acid (Scholl.

TIPS-anthracene | 862667-06-9

Anthracène — Wikipédi

アントラセン - Wikipedi

Macroscale organisms maintain a high degree of orderliness on an extremely small scale. Inspired by natural assemblies, anthracene-based organoplatinum metallacycles were designed as building blocks. Instead of the expected planar rectangles, a highly twisted structure was generated due to strong π···π stacking interactions and steric hindrance between the two anthracene ligands The anthracene moieties of the Chro dimer is sandwiched and mutually stacked between the C-D glycosidic linkage of the other Chro monomer and the ribose of C6, bringing the backbone of the DNA duplex towards the ligand direction in order to stabilize the ligand-DNA complex (Supplementary Figure S9). This is similar to the packing interaction.

Here limiting reagent is anthracene; hence yield should be calculated from its amount taken. Molecular formula of anthracene = C18H10. Molecular formula of 9,10-dihydroanthracene-9,10-endo-α,β-succinic anhydride = ‎C18H12O3. Molecular weight of anthracene = 178 g/mole. Molecular weight of 9,10-dihydroanthracene-9,10-endo-α,β. anthracene oil: [noun] a heavy green oil that distills over from coal tar above 270° C and is the principal source of anthracene, phenanthrene, and carbazole Anthracene nanocrystals under an optical polarization microscope (polarizer and analyser are crossed). Images (a) and (b) are taken at different orientations of the sample with respect to the field of view (orientation of polarizer (analyser) is fixed). Four types of labels (circle, square, triangle and hexagon) are introduced to ease tracing. Anthracene was added as a 0.5% ethereal spray (w/v) on the surfaces of solid medium as described by Kiyohara . Anthracene was dissolved in dimethylformamide at 25 mg ml −1 and added to liquid medium to give a final concentration of 25 μg ml −1. 2.3 Mass balance experiment

蒽 - 維基百科,自由的百科全

Anthracene Oil at Best Price in India

Their catalytic performance for anthracene hydrogenation was evaluated using a slurry-bed batch reactor with an initial hydrogen pressure of 80 bar at 350 °C for 4 h. The intercalated MoS2 nanoflowers synthesized from Na2MoO4 (MoS2-S) and H2MoO4 (MoS2-A) as molybdenum precursors have diameters of about 150 and 50 nm, respectively The preparation of two types of anthracene dimer is described and their absorption and fluorescence spectra are reported. The basic spectral features of each dimer, together with a consideration of the method of formation, enable us to assign a geometry to each pair Aggregation-induced emission enhancement of anthracene-derived Schiff base compounds and their application as a sensor for bovine serum albumin and optical cell imaging. Simon Densil, Simon Densil. Department of Chemistry, V. O. Chidambaram College, Thoothukudi, India including benz[a]anthracene, benzo[a]pyrene, benzo[b]fluoranthene, benzo[j]fluoranthene, benzo[k]fluoranthene, chrysene, dibenz[a,h]anthracene, and indeno [1,2,3-c,d]pyrene, have caused tumors in laboratory animals when they breathed these substances in the air, when they ate them, or when they had long periods of skin contact with them

The modulatory effect of taurine on 7,12-dimethylbenz(a)anthracene (DMBA)-induced breast cancer in rats was studied. DMBA (25 mg/kg body weight) was administered to induce breast cancer in rats. Protein carbonyl levels, activities of membrane bound enzymes (Na(+) /K(+) ATPase, Ca(2+) ATPase, and Mg( Structure, properties, spectra, suppliers and links for: Benz(a)anthracene, 56-55-3 < 0.01). Other possible effects of anthracene were not reported. There were three cases of epithelioma (hand, cheek, and wrist) that were reported in men who routinely handled 40% crude anthracene in an alizarin factory (Kennaway, 1924a,b). Two of these workers handled anthracene for 30-32 years and had never worked with any other coal-tar. Anthracene oil, also called green oil, consists of three benzene rings derived from coal tar. Anthracene oil is used in the production of carbon black. It is also a source of phenanthrene, anthracene and carbazole. This oil is considered the best antiseptic agent for wood and is so used for formulating sleeper-impregnating oils Anthracene Assembled Hydrocarbon. An anthracene is a fascinating building unit to construct novel aromatic hydrocarbons. Its fluorescent properties have been applied to develop emissive materials such as functional dyes and sensing probes. When multiple anthracene units are assembled in a molecule, the photophysical properties are considerably.

Simple and easily accessible anthracene dyes with

Anthracene-2,6-disulfonate can be crystallised with various simple alkylammonium ions and, in the case of + N(CH 3) 2 (C 16 H 33) 2, a crystal structure determination has shown that the long paraffinic chains are intercalated between the anthracene moieties. The dianion forms columnar mesophases with trialkoxybenzylimidazolium cations, as. A chemical sensor that can induce near-infrared red-shifted response represents a promising strategy for the design and development of anion probes. In this work, novel CH-controlled colorimetric probe 3 based on anthracene carboximide was developed for near-infrared detection of cyanide. Probe 3 consisted of CHCN binding site to anthracene carboximide fluorophore, and showed a significant.

The anaerobic anthracene biodegradation activity of V. parvula isolates from non-smokers was the highest among all isolates of the three recovered genera from the same subject. The anthracene biodegradation potential of Lactobacillus spp. was variable In the anthracene landing on the process, the two carbon atoms from C 60 are puckered out of the cage surface, the structure of C 14 H 10 is modified to allow the 9, 10 C-atoms to bond to the C-atoms from the fullerene (Sato et al. 2013)

Anthracene - omlc.or

Anthracene CAS#: 120-12-

Human Carbonic anhydrase II bound by anthracene-9-sulfonamide. In the design of high-affinity and enzyme isoform-selective inhibitors, we applied an approach of augmenting the substituents attached to the benzenesulfonamide scaffold in three ways, namely, substitutions at the 3,5- or 2,4,6-positions or expansion of the condensed ring system anthracene and 9-substituted anthracene derivatives, with either 1-octylmaleimide or maleic anhydride as a dienophile, assisted by their crystal structures could serve as a reference for such an endeavor. An octylmaleimide Diels-Alder adducts of anthracene (1) and a 9-substituted derivative (2) were obtained by reacting the corre 53-70-3 - LHRCREOYAASXPZ-UHFFFAOYSA-N - Dibenz(a,h)anthracene - Similar structures search, synonyms, formulas, resource links, and other chemical information 20 Anthracene oil, anthracene paste, distn. lights 91995-17-4 1/13/2010 21 Anthracene oil, anthracene-low 90640-82-7 1/13/2010 22 Diisobutyl phthalate 84-69-5 1/13/2010 23 Lead chromate 7758-97-6 1/13/2010 24 Lead chromate molybdate sulphate red (C.I. Pigment Red 104) 12656-85-8 1/13/2010.

Antracene - Wikipedi

Anthracene-9,10-dipropionic acid disodium salt (CAS 82767-90-6) 参考价格: 询价. 品 牌: santacruze. 货 号: sc-396571. cas号: 82767-90-6. 分 子 量: 366.32. 分 子 式: C20H16Na2O4 A novel series of thiophenes having biologically active sulfonamide (2-11), 3-methylisoxazole (12), 4-methoxybenzo[d]thiazole (13), quinoline (14, 15), benzoylphenylamino (16) and anthracene-9,10-dione (17) moieties were prepared. Structures of the newly synthesized compounds were established by elemental analysis and spectral data Schiff base derived from thiosemicarbazone and anthracene showed high potential in overcoming multidrug resistance in vitro with low drug resistance index Jie Bai,1 Rui-Hui Wang,1 Yan Qiao,2 Aidong Wang,3 Chen-Jie Fang1 1Department of Chemical Biology, School of Pharmaceutical Sciences, Capital Medical University, Beijing, 2Department of Pathophysiology, School of Basic Medical Sciences. adenocarcinomas in vivo (6). 7,12-Dimethylbenz[a]anthracene (DMBA)andN-nitrosomethylurea(NMU) were chosenfor use because they are known carcinogens for the rat mammar

Anthracene-D10 C14H10 - PubChe

7,12-Dimethylbenz[a]anthracene. text.skipToContent text.skipToNavigation. TCI uses cookies to personalize and improve your user experience. By continuing on our website, you accept the use of cookies. You can change or update your cookiesettings at any time. Accept Research article Electron and proton magnetic resonance spectroscopic investigation of anthracene oxidation Mohamed A. Morsya,*, Abdel-Nasser M. Kawdeb, Muhammad Kamrana, Thomas F. Garrisona, Wissam Ialia, Salman S. Alharthic a Chemistry Department, College of Chemicals and Materials, King Fahd University of Petroleum & Minerals, P.O. Box 1624, Dhahran 31261, Saudi Arabi

AnthraceneKekulenes, cycloarenes, and heterocycloarenes: addressing