3-(Ethylamino)-p-kresol
|
|
- CAS-Nr.
- 120-37-6
- Bezeichnung:
- 3-(Ethylamino)-p-kresol
- Englisch Name:
- 3-Ethylamino-4-methylphenol
- Synonyma:
- 3-Ethylamino;3-Ethylamino-4-kresol;3-ETHYLAMINO-4-CRESOL;3-(ETHYLAMINO)-P-CRESOL;3-Ethylamino-p-cresol>3-ETHYLAMINO-4-METHYLPHENOL;3-Ethylamino-p-cresol;5-Ethylamino-p-cresol (OH=1);4-Methyl-3-ethylaminophenol.;3-Ethylamino-p-cresol (OH=1)
- CBNumber:
- CB5104572
- Summenformel:
- C9H13NO
- Molgewicht:
- 151.21
- MOL-Datei:
- 120-37-6.mol
|
3-(Ethylamino)-p-kresol Eigenschaften
- Schmelzpunkt:
- 85-87 °C (lit.)
- Siedepunkt:
- 135-140°C 3mm
- Dichte
- 1.0406 (rough estimate)
- Brechungsindex
- 1.5380 (estimate)
- Flammpunkt:
- 135-140°C/3mm
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- pka
- 10.66±0.18(Predicted)
- Aggregatzustand
- powder to crystal
- Farbe
- White to Gray to Red
- Wasserl?slichkeit
- Insoluble in water.
- BRN
- 3241548
- Stabilit?t:
- Stable. Incompatible with strong oxidizing agents.
- CAS Datenbank
- 120-37-6(CAS DataBase Reference)
- NIST chemische Informationen
- Phenol, 3-(ethylamino)-4-methyl-(120-37-6)
- EPA chemische Informationen
- 3-(Ethylamino)-4-methylphenol (120-37-6)
Sicherheit
- Risiko- und Sicherheitserkl?rung
- Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher |
Xi |
|
|
R-S?tze: |
36/37/38 |
|
|
S-S?tze: |
26-37/39 |
|
|
WGK Germany |
2 |
|
|
RTECS-Nr. |
SL4105000 |
|
|
TSCA |
Yes |
|
|
HS Code |
29222990 |
|
|
Bildanzeige (GHS) |
|
Alarmwort |
Warnung |
Gefahrenhinweise |
Code |
Gefahrenhinweise |
Gefahrenklasse |
Abteilung |
Alarmwort |
Symbol |
P-Code |
H315 |
Verursacht Hautreizungen. |
Hautreizung |
Kategorie 2 |
Warnung |
src="/GHS07.jpg" width="20" height="20" /> |
P264, P280, P302+P352, P321,P332+P313, P362 |
H319 |
Verursacht schwere Augenreizung. |
Schwere Augenreizung |
Kategorie 2 |
Warnung |
src="/GHS07.jpg" width="20" height="20" /> |
P264, P280, P305+P351+P338,P337+P313P |
H335 |
Kann die Atemwege reizen. |
Spezifische Zielorgan-Toxizit?t (einmalige Exposition) |
Kategorie 3 (Atemwegsreizung) |
Warnung |
src="/GHS07.jpg" width="20" height="20" /> |
|
|
Sicherheit |
P261 |
Einatmen von Staub vermeiden. |
P264 |
Nach Gebrauch gründlich waschen. |
P264 |
Nach Gebrauch gründlich waschen. |
P271 |
Nur im Freien oder in gut belüfteten R?umen verwenden. |
P280 |
Schutzhandschuhe/Schutzkleidung/Augenschutz tragen. |
P302+P352 |
BEI BERüHRUNG MIT DER HAUT: Mit viel Wasser/... (Hersteller kann, falls zweckm??ig, ein Reinigungsmittel angeben oder, wenn Wasser eindeutig ungeeignet ist, ein alternatives Mittel empfehlen) waschen. |
P305+P351+P338 |
BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach M?glichkeit entfernen. Weiter spülen. |
|
3-(Ethylamino)-p-kresol Chemische Eigenschaften,Einsatz,Produktion Methoden
R-S?tze Betriebsanweisung:
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-S?tze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S37/39:Bei der Arbeit geeignete Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
Chemische Eigenschaften
purple solid
Verwenden
3-Ethylamino-4-methylphenol was used in the synthesis of rhodol by undergoing condensation reaction with 2-(2,4-dihydroxybenzoyl)benzoic acid.
Allgemeine Beschreibung
Purple solid.
Air & Water Reaktionen
3-Ethylamino-4-methylphenol may be sensitive to prolonged exposure to air. . Insoluble in water.
Reaktivit?t anzeigen
An amine and phenol. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Phenols do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases. Such heating may initiate polymerization of the organic compound. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). The reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid.
Brandgefahr
Flash point data for 3-Ethylamino-4-methylphenol are not available. 3-Ethylamino-4-methylphenol is probably combustible.
3-(Ethylamino)-p-kresol Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
3-(Ethylamino)-p-kresol Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.
Global( 193)Lieferanten
120-37-6(3-(Ethylamino)-p-kresol)Verwandte Suche:
- 1-Methyl-2-(ethylamino)-4-hydroxybenzene
- 2-Ethylamino-4-hydroxy-1-methylbenzene
- 3-Ethylamino-p-cresol
- 3-(ethylamino)-4-methyl-pheno
- 3-Ethylamino
- 3-ETHYLAMINO-PARAMETHYLPHENOL
- 3-(ETHYLAMINO)-P-CRESOL
- 3-ETHYLAMINO-4-CRESOL
- 3-ETHYLAMINO-4-METHYLPHENOL
- 4-Methyl-3-(N-ethylamino)-phenol
- 3-Ethylamino-4-kresol
- 3-ETHYLAMINO-4-METHYLPHENOL: TECH., 90%
- 5-Ethylamino-p-cresol (OH=1)
- 2-Ethylamino-4-hydroxytoluene
- 4-Methyl-3-ethylaminophenol.
- 3-Ethylamino-p-cresol (OH=1)
- 3-Ethylamino-p-cresol>
- Phenol, 3-(ethylamino)-4-methyl-
- 3-Ethylamino-4-methylphenol ISO 9001:2015 REACH
- TIANFUCHEM 120-37-6 3-Ethylamino-4-methylphenol
- 120-37-6
- C2H5NHC6H3CH3OH
- Phenols
- Oxygen Compounds
- Organic Building Blocks
- Building Blocks
- Building Blocks
- C9 to C20+
- Chemical Synthesis
- Organic Building Blocks
- Oxygen Compounds
- Intermediates of Dyes and Pigments
- Organic Building Blocks
- Oxygen Compounds
- Phenols