Dioxybenzon

Bezeichnung:Dioxybenzon

CAS-Nr131-53-3

Englisch Name:2,2'-Dihydroxy-4-methoxybenzophenone

CBNumberCB5191699

SummenformelC14H12O4

Molgewicht244.24

MOL-Datei131-53-3.mol

Synonyma

Dioxybenzon

Dioxybenzon physikalisch-chemischer Eigenschaften

Schmelzpunkt	73-75 °C(lit.)
Siedepunkt	170-175 °C1 mm Hg(lit.)
Dichte	1.2379 (rough estimate)
Dampfdruck	0-0Pa at 20-25℃
Brechungsindex	1.5389 (estimate)
storage temp.	Sealed in dry,Room Temperature
Löslichkeit	DMSO (Slightly), Methanol (Slightly)
pka	7.11±0.35(Predicted)
Aggregatzustand	Solid
Farbe	Off-White to Yellow
Merck	14,3303
Stabilität	Stable. Incompatible with strong oxidizing agents.
InChIKey	MEZZCSHVIGVWFI-UHFFFAOYSA-N
LogP	2.33 at 23.5℃
CAS Datenbank	131-53-3(CAS DataBase Reference)
NIST chemische Informationen	Dioxybenzone(131-53-3)
EPA chemische Informationen	Dioxybenzone (131-53-3)

Sicherheit

Kennzeichnung gefährlicher	Xi
R-Sätze:	36/37/38
S-Sätze:	26-36
WGK Germany	3
RTECS-Nr.	DJ1049500
HS Code	29145090
Giftige Stoffe Daten	131-53-3(Hazardous Substances Data)

Gefahreninformationscode (GHS)

2,2'-Dihydroxy-4-methoxybenzophenone Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
Chemische Eigenschaften
Light yellow powder. Freezing point 68℃, boiling point 170-175℃(0.133kPa), relative density 1.382(25℃).Solubility at 25℃(g/100g solvent): benzene 46.6, n-hexane 2.3, 95% ethanol 21.4, carbon tetrachloride 22.2, methylethyl ketone 55.3, plasticiser DOP 31.1, insoluble in water.
Application
Dioxybenzone is a compound used in sunscreen formulations to block out UVB and UVA harmful rays. Broad-spectrum sunscreens often contain a number of chemical ingredients that absorb UVA and UVB radiation. Many sunscreens contain UVA-absorbing avobenzone or a benzophenone (such as dioxybenzone, oxybenzone, or sulisobenzone), in addition to UVB-absorbing chemical ingredients (some of which also contribute to UVA protection).
Verwenden
benzophenone-8 (dioxybenzone) is an FDA-approved sunscreen chemical with uVA-absorption capabilities. It also can protect product degradation arising from uV-light exposure. It has an approved usage level of 3 percent in the united States.
synthetische
preparation by condensation of salicylic acid and m-methoxyphenol.
Definition
ChEBI: 2,2'-Dihydroxy-4-methoxybenzophenone is a member of benzophenones.
Allgemeine Beschreibung
Dioxybenzone, also known as benzophenone-8, is an organic compound and a derivative of benzophenone used commercially in sunscreens. It absorbed UV-B and UV-AII rays. Dioxybenzone is an approved sunscreen ingredient in concentrations up to 3%.
Reaktivität anzeigen
An alcohol and a ketone. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides. Ketones are reactive with many acids and bases liberating heat and flammable gases (e.g., H2). The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone. Ketones react with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable gas (H2) and heat. Ketones are incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides. They react violently with aldehydes, HNO3, HNO3 + H2O2, and HClO4.
Brandgefahr
Flash point data for 2,2'-Dihydroxy-4-methoxybenzophenone are not available. 2,2'-Dihydroxy-4-methoxybenzophenone is probably combustible.

2,2'-Dihydroxy-4-methoxybenzophenone Upstream-Materialien And Downstream Produkte

Dioxybenzon Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

131-53-3, 2,2'-Dihydroxy-4-methoxybenzophenone Verwandte Suche:

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