Dibenzylamin

Bezeichnung:Dibenzylamin

CAS-Nr103-49-1

Englisch Name:Dibenzylamine

CBNumberCB5185977

SummenformelC14H15N

Molgewicht197.28

MOL-Datei103-49-1.mol

Synonyma

Dibenzylamin

Dibenzylamin physikalisch-chemischer Eigenschaften

Schmelzpunkt	-26 °C (lit.)
Siedepunkt	300 °C (lit.)
Dichte	1.026 g/mL at 25 °C (lit.)
Dampfdruck	1-1013hPa at 113.1-286℃
Brechungsindex	n20/D 1.574(lit.)
Flammpunkt	290 °F
storage temp.	Keep in dark place,Inert atmosphere,Room temperature
Löslichkeit	0.4g/l
Aggregatzustand	Liquid
pka	pK1:8.52(+1) (25°C)
Farbe	Clear colorless to light yellow
PH	8.9 (H2O, 20℃)
Geruch (Odor)	ammonia-like odor
Wasserlöslichkeit	0.05 g/L (20 ºC)
Merck	14,3011
BRN	909664
Dielectric constant	3.6（20℃）
Stabilität	Stable. Incompatible with oxidizing agents, acid anhydrides, acids, acid chlorides, chloroformates.
InChIKey	BWLUMTFWVZZZND-UHFFFAOYSA-N
LogP	2.67 at 20℃
CAS Datenbank	103-49-1(CAS DataBase Reference)
NIST chemische Informationen	Dibenzylamine(103-49-1)
EPA chemische Informationen	Dibenzylamine (103-49-1)

Sicherheit

Kennzeichnung gefährlicher	Xn,Xi,C
R-Sätze:	22-36/38-52/53-34
S-Sätze:	26-61-45-36/37/39
RIDADR	2810
WGK Germany	3
Hazard Note	Irritant/Corrosive
TSCA	Yes
HazardClass	8
PackingGroup	III
HS Code	29214980

Gefahreninformationscode (GHS)

Dibenzylamine Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R22:Gesundheitsschädlich beim Verschlucken.
R36/38:Reizt die Augen und die Haut.
R52/53:Schädlich für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R34:Verursacht Verätzungen.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
Beschreibung
Dibenzyl amine (Dibenzylamine), molecular formula C14H15N, molecular weight 197.28, specific density 1.026, fusing point-26 ℃, 300 ℃ of boiling points, specific refractory power 1.574-1.576,143 ℃ of flash-points, water-soluble 0.05G/L (20 ℃). Dibenzyl amine is a colourless oil liquid, is smelly of ammonia, is soluble in ethanol and ether, and is water insoluble. Skin and mucous membranes have a stronger pungency. Dibenzyl amine is an important organic synthesis intermediate. Because dibenzylamine can not derive any carcinogenic nitrosamine and be widely used in the building-up process of medicine such as penicillin, and Linezolid, simultaneously, dibenzylamine can be used for producing the vulcanization accelerator zinc dibenzyldithiocarbamate (ZBEC) of high effect nontoxic and tetra-benzyl thiram disulfide (TBZTD) and can be used for the mensuration of cobalt, iron, cyanate etc.
Chemische Eigenschaften
colorless to light yellow oily liquid with ammonia odor. soluble in ethanol and ether, insoluble in water.
Verwenden
Dibenzylamine is used to prepare rubber accelerator for the vulcanization process and reaction-stoppers. Dibenzylamine type accelerators reduce nitrosamine production in the compounding process. It is also used to produce dibenzyl-nitroso-amine.
Definition
ChEBI: Dibenzylamine is an aromatic amine.
synthetische
Dibenzylamine is obtained by the reaction of benzyl chloride and liquid ammonia in ethanol.
Application
Dibenzylamine is an important organic synthesis intermediate, mainly used to produce efficient and non-toxic vulcanization accelerators tetrabenzylthiuramdisulfide (TBZTD) and zinc dibenzyldithiocarbamate (ZBEC). Synthesize penicillin and curing agent for rubber and plastic curing, and can be used in the detection of cobalt, cyanate, and iron.
Biologische Funktion
Dibenzylamine (DBA) has anticonvulsant effects. It can block NMDA-evoked currents in a concentration and voltage-dependent manner. This conclusion was researched in an audiogenic seizure-susceptible mouse model. It possesses antiproliferative properties and could be of interest for the development of new antitumor drugs.
Synthesis Reference(s)
Tetrahedron Letters, 26, p. 4633, 1985 DOI: 10.1016/S0040-4039(00)98771-9
The Journal of Organic Chemistry, 60, p. 5969, 1995 DOI: 10.1021/jo00123a041
Hazard
Dibenzylamine is danger.
H302 (99.32%): Harmful if swallowed [Warning Acute toxicity, oral]
H314 (57.43%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
H315 (42.57%): Causes skin irritation [Warning Skin corrosion/irritation]
H319 (42.57%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
H412 (32.43%): Harmful to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard]
Synthese
The synthesis process of dibenzylamine comprises the following steps: reacting raw materials (benzaldehyde and ammonium hydroxide) for 20-70min at 60-120 DEG C under a hydrogen pressure of 0.5-2.0MPa in the presence of a catalyst, wherein alcohol with 1-4 carbon atoms can be added optionally to serve as an organic solvent and a phase transfer catalyst can be added optionally; by the end of the reaction, cooling, filtering to recover the catalyst, layering the filtrate to obtain a dibenzylamine product; and recycling and reusing excessive ammonium hydroxide.
läuterung methode
Purify the amine by distillation in a vacuum. It causes burns to the skin. The dihydrochloride has m 265-266o (from MeOH/HCl), and the tetraphenyl boronate has m 129-133o. [Bradley & Maisey J Chem Soc 247 1954, Hall J Phys Chem 60 63 1956, Donetti & Bellora J Org Chem 37 3352 1972, Beilstein 12 IV 2179.]

Dibenzylamine Upstream-Materialien And Downstream Produkte

Dibenzylamin Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

103-49-1, Dibenzylamine Verwandte Suche:

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