Cookies disclaimer

I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.

131-56-6 - 2,4-Dihydroxybenzophenone, 99% - A13749 - Alfa Aesar

A13749 2,4-Dihydroxybenzophenone, 99%

CAS Number
131-56-6
Synonyms

Size Price ($) Quantity Availability
100g 25.24
500g 91.77
2500g 324.80
Add to Cart Add to Quote Request View Item

2,4-Dihydroxybenzophenone, 99%

MDL
MFCD00002277
EINECS
205-029-4

Chemical Properties

Formula
C13H10O3
Formula Weight
214.22
Melting point
144-147°
Boiling Point
194°/1mm
Flash Point
125°(257°F)
Density
1.320
Solubility
Insoluble in water.

Applications

Novel mordent and disperse azo dyes were prepared by the coupling of various diazo solutions of aromatic amines with 2, 4-dihydroxybenzophenone. The ultraviolet absorbing monomers were synthesized by reaction of 2, 4-dihydroxybenzophenone with glycidyl acrylate and glycidyl methacrylate. Two new polymerizable stabilizers, 4-benzoyl-2-(α-piperidino-2-chlorobenzyl)-3-hydroxyphenyl acrylate (BPBHA) and corresponding methacrylate (BPBHMA), were synthesized and characterized from 2,4-Dihydroxybenzophenone. a polymerizable UV-stabilizer, 2-hydroxy-4-(3-methacryloxy-2-hydroxylpropoxy) benzophenone (BPMA), was synthesized using 2, 4-dihydroxybenzophenone (UV-0) and glycidyl methacrylate (GMA).

Notes

Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.

Literature References

J. Fertig,; A. I. Goldberg,; M. Skoultchi. Ultraviolet stabilizing monomers and polymers. II. Synthesis and polymerization of acrylate and methacrylate derivatives of 2,4-dihydroxybenzophenone†. Journal of Applied Polymer Science1966, 10 (4), 663-672.

Lodewyk J. Mienie,; Jacobus J. Bergh,; Jeffrey R. Bloomquist,; Neal Castagnoli Jr,; Stefanus J. Steyn,; Cornelis J. Van der Schyf. p-Fluorophenylglycine in the urine of baboons treated with HPTP, the tetrahydropyridine analog of haloperido. Life Sciences. 1999, 65(5), 535-542.

GHS Hazard and Precautionary Statements

Hazard Statements: H319

Causes serious eye irritation.

Precautionary Statements: P280-P264-P305+P351+P338-P337+P313

Wear protective gloves/protective clothing/eye protection/face protection. Wash thoroughly after handling. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. If eye irritation persists: Get medical advice/attention.

Other References

Merck
14,1106
Beilstein
1311566
Harmonized Tariff Code
2914.50
TSCA
Yes
RTECS
DJ0700000

Recommended

  • A10237

    2,2',4,4'-Tetrahydroxybenzophenone, 98+%
  • A12646

    Triethylamine, 99%
  • A13172

    Ethyl 4-hydroxybenzoate, 99%
  • A14455

    2-Chloroethylamine hydrochloride, 98+%
  • A17662

    2-Hydroxy-4-methoxybenzophenone, 98+%

Recently Viewed

Chemicals

Life Science

Metals & Materials

Catalysts

Analytical & Labware