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Nafenopin

Nafenopin Struktur
3771-19-5
CAS-Nr.
3771-19-5
Englisch Name:
Nafenopin
Synonyma:
TPIA;Melipan;Su-13437;Nafenopin;C-13437Su;CIBA-13437Su;Nafenopin USP/EP/BP;2-methyl-2-(4-tetralin-1-ylphenoxy)propionic acid;2-METHYL-2-PARA-(1,2,3,4-TETRAHYDRO-1-NAPHTHYL)PHENOXYPROPIONICACID;2-methyl-2-[4-(1,2,3,4-tetrahydronaphthalen-1-yl)phenoxy]propanoicaci
CBNumber:
CB61116627
Summenformel:
C20H22O3
Molgewicht:
310.39
MOL-Datei:
3771-19-5.mol

Nafenopin Eigenschaften

Schmelzpunkt:
117-118 °C
Siedepunkt:
390.55°C (rough estimate)
Dichte
1.1662 (rough estimate)
Brechungsindex
1.4618 (estimate)
storage temp. 
Sealed in dry,Room Temperature
pka
3.28±0.10(Predicted)
Aussehen
white solid
IARC
2B (Vol. 24, Sup 7) 1987
EPA chemische Informationen
Nafenopin (3771-19-5)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Bildanzeige (GHS) Exclamation Mark (GHS07)Health Hazard (GHS08)
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H302 Gesundheitssch?dlich bei Verschlucken. Akute Toxizit?t oral Kategorie 4 Warnung P264, P270, P301+P312, P330, P501
H351 Kann vermutlich Krebs verursachen. Karzinogenit?t Kategorie 2 Warnung P201, P202, P281, P308+P313, P405,P501
H361 Kann vermutlich die Fruchtbarkeit beeintr?chtigen oder das Kind im Mutterleib sch?digen. Reproduktionstoxizit?t Kategorie 2 Warnung P201, P202, P281, P308+P313, P405,P501
Sicherheit
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach M?glichkeit entfernen. Weiter spülen.

Nafenopin Chemische Eigenschaften,Einsatz,Produktion Methoden

Definition

ChEBI: A monocarboxylic acid that is 2-hydroxy-2-methylpropanoic acid in which ther tertiary hydroxy group has been converted to the corresponding p-(1,2,3,4-tetrahydronaphthalen-1-yl)phenyl ether.

Allgemeine Beschreibung

Crystals.

Reaktivit?t anzeigen

An organic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in Nafenopin to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible.

Brandgefahr

Flash point data for Nafenopin are not available. Nafenopin is probably combustible.

Sicherheitsprofil

Confirmed carcinogen with experimental carcinogenic and tumorigenic data. Moderately toxic by ingestion. Mutation data reported. A drug for the treatment of hypercholesterolemia or hypertriglyceridemia. When heated to decomposition it emits acrid smoke and irritating fumes.

Nafenopin Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Nafenopin Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 25)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354
marketing@targetmol.com United States 32467 58
Career Henan Chemica Co
+86-0371-86658258 +8613203830695
laboratory@coreychem.com China 30224 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167
1026@dideu.com China 9996 58
InvivoChem
+1-708-310-1919 +1-13798911105
sales@invivochem.cn United States 6391 58
TargetMol Chemicals Inc.
+17819995354
marketing@targetmol.com United States 19956 58
BOC Sciences 1-631-485-4226; 16314854226
info@bocsci.com United States 9920 65
Shanghai AQBioPharma Co., Ltd. 13661411401
yinglv.que@aqbiopharma.com.cn China 2977 58
3A Chemicals 400-668-9898
service@3achem.com China 20557 58
Chengdu Saint - Kay Biotechnology Co., Ltd. 028-85157043 15882256948
676046971@qq.com China 4191 58
Shanghai Jizhi Biochemical Technology Co. Ltd. 021-4009004166/18616739031 18616739031
3007523370@qq.com China 52678 58

  • Nafenopin
  • 2-METHYL-2-PARA-(1,2,3,4-TETRAHYDRO-1-NAPHTHYL)PHENOXYPROPIONICACID
  • C-13437Su
  • CIBA-13437Su
  • Melipan
  • Su-13437
  • TPIA
  • 2-methyl-2-(4-tetralin-1-ylphenoxy)propionic acid
  • 2-methyl-2-[4-(1,2,3,4-tetrahydronaphthalen-1-yl)phenoxy]propanoic acid
  • Propanoic acid, 2-methyl-2-[4-(1,2,3,4-tetrahydro-1-naphthalenyl)phenoxy]-
  • 2-methyl-2-[4-(1,2,3,4-tetrahydronaphthalen-1-yl)phenoxy]propanoicaci
  • Nafenopin USP/EP/BP
  • 3771-19-5
  • C20H22O3
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