(2,4-dihydroxyphenyl)-phenyl-methanone (CAS 92092-63-2) — formula C13H10O3, molecular weight 214.22; category organic chemicals.
| CAS Number | 92092-63-2 |
|---|---|
| Molecular Formula | C13H10O3 |
| Molecular Weight | 214.22 |
| Melting Point | 144 °C |
| Boiling Point | BP: 194 °C at 1 mm Hg |
| LogP | 3.2 |
| Applications | Uses: CIR ingredient: Benzophenone-1, Used as an ultraviolet absorber in polymers, sunscreening agent, and ultraviolet stabilizer for polymers, [HSDB] Used as an ultraviolet light absorber in paints, [Merck Index], Painting (Pigments, Binders, and Biocides) [Category: Paint], Plastic Composites Manufacturing [Category: Industry], Ultraviolet light absorber, especially in paints and plastics., Ultraviolet absorber in polymers, Used as sunscreening agent., SRP: Former use, Use Classification: Fragrance Ingredients, Cosmetics -> Uv absorber, Household Products: Information on 28 consumer products that contain Benzophenone-1 in the following categories is provided:, • Auto Products, • Personal Care, Methods of Manufacturing: 2, 4-Dihydroxybenzophenone ... is formed in 90% yield by the uncatalyzed reaction of benzotrichloride with resorcinol in hydroxylic solvents or in benzene containing methanol or ethanol., Three methods of Benzophenone-1 preparation from resorcinol are reported. Stephen and Zilberman and Rybakova prepared Benzophenone-1 from the Hoesch reaction of resorcinol and either a substituted imido chloride (to form an imido-ester intermediate) or a corresponding aromatic nitrile and a metal halide catalyst. Shaw and Mehta described the condensation of benzamide with resorcinol in the presence of phosphorous oxychloride and zinc chloride to Benzophenone-1. Additionally, Benzophenone-1 can be prepared in low yield by the Fries rearrangement from phenyl-2-methoxy-benzoate., U.S. Production: (1977) AT LEAST 4.54X10+7 GRAMS, (1981) No Data, Non-confidential 2012 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Methanone, (2, 4-dihydroxyphenyl)phenyl-. National Production Volume: 31, 680 lb, yr., Non-confidential 2016 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Methanone, 4-dihydroxyphenyl)phenyl-:, Table: National Aggregate Production Volume (pounds) [Table#5461], U.S. Imports: (1979) No Data, (1981) 3.75X10+5 GRAMS (PRINCPL CUSTMS DISTS), U.S. Exports: (1979) No Data, General Manufacturing Information: Methanone, 4-dihydroxyphenyl)phenyl-: ACTIVE |
| Category | Organic Chemicals |
Documented applications: Uses: CIR ingredient: Benzophenone-1, Used as an ultraviolet absorber in polymers, sunscreening agent, and ultraviolet stabilizer for polymers, [HSDB] Used as an ultraviolet light absorber in paints, [Merck Index], Painting (Pigments, Binders, and Biocides) [Category: Paint], Plastic Composites Manufacturing [Category: Industry], Ultraviolet light absorber, especially in paints and plastics., Ultraviolet absorber in polymers, Used as sunscreening agent., SRP: Former use, Use Classification: Fragrance Ingredients, Cosmetics -> Uv absorber, Household Products: Information on 28 consumer products that contain Benzophenone-1 in the following categories is provided:, • Auto Products, • Personal Care, Methods of Manufacturing: 2, 4-Dihydroxybenzophenone ... is formed in 90% yield by the uncatalyzed reaction of benzotrichloride with resorcinol in hydroxylic solvents or in benzene containing methanol or ethanol., Three methods of Benzophenone-1 preparation from resorcinol are reported. Stephen and Zilberman and Rybakova prepared Benzophenone-1 from the Hoesch reaction of resorcinol and either a substituted imido chloride (to form an imido-ester intermediate) or a corresponding aromatic nitrile and a metal halide catalyst. Shaw and Mehta described the condensation of benzamide with resorcinol in the presence of phosphorous oxychloride and zinc chloride to Benzophenone-1. Additionally, Benzophenone-1 can be prepared in low yield by the Fries rearrangement from phenyl-2-methoxy-benzoate., U.S. Production: (1977) AT LEAST 4.54X10+7 GRAMS, (1981) No Data, Non-confidential 2012 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Methanone, (2, 4-dihydroxyphenyl)phenyl-. National Production Volume: 31, 680 lb, yr., Non-confidential 2016 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Methanone, 4-dihydroxyphenyl)phenyl-:, Table: National Aggregate Production Volume (pounds) [Table#5461], U.S. Imports: (1979) No Data, (1981) 3.75X10+5 GRAMS (PRINCPL CUSTMS DISTS), U.S. Exports: (1979) No Data, General Manufacturing Information: Methanone, 4-dihydroxyphenyl)phenyl-: ACTIVE.
(2,4-dihydroxyphenyl)-phenyl-methanone is a carbon-based organic compound with CAS registry number 92092-63-2 and molecular formula C13H10O3 (molecular weight 214.22), belonging to the organic chemicals segment of chemical raw materials.
CAS number: 92092-63-2
Its molecular formula C13H10O3 comprises 13 C, 10 H, 3 O atoms.
Also known as: (2,4-dihydroxyphenyl)-phenyl-methanone · (2,4-二羟基苯基)-苯基甲酮
Category: organic chemicals
The CAS registry number of (2,4-dihydroxyphenyl)-phenyl-methanone is 92092-63-2.
Molecular formula C13H10O3, molecular weight 214.22.
It is also registered under: (2,4-dihydroxyphenyl)-phenyl-methanone, (2,4-二羟基苯基)-苯基甲酮.
Recorded applications: Uses: CIR ingredient: Benzophenone-1, Used as an ultraviolet absorber in polymers, sunscreening agent, and ultraviolet stabilizer for polymers, [HSDB] Used as an ultraviolet light absorber in paints, [Merck Index], Painting (Pigments, Binders, and Biocides) [Category: Paint], Plastic Composites Manufacturing [Category: Industry], Ultraviolet light absorber, especially in paints and plastics., Ultraviolet absorber in polymers, Used as sunscreening agent., SRP: Former use, Use Classification: Fragrance Ingredients, Cosmetics -> Uv absorber, Household Products: Information on 28 consumer products that contain Benzophenone-1 in the following categories is provided:, • Auto Products, • Personal Care, Methods of Manufacturing: 2, 4-Dihydroxybenzophenone ... is formed in 90% yield by the uncatalyzed reaction of benzotrichloride with resorcinol in hydroxylic solvents or in benzene containing methanol or ethanol., Three methods of Benzophenone-1 preparation from resorcinol are reported. Stephen and Zilberman and Rybakova prepared Benzophenone-1 from the Hoesch reaction of resorcinol and either a substituted imido chloride (to form an imido-ester intermediate) or a corresponding aromatic nitrile and a metal halide catalyst. Shaw and Mehta described the condensation of benzamide with resorcinol in the presence of phosphorous oxychloride and zinc chloride to Benzophenone-1. Additionally, Benzophenone-1 can be prepared in low yield by the Fries rearrangement from phenyl-2-methoxy-benzoate., U.S. Production: (1977) AT LEAST 4.54X10+7 GRAMS, (1981) No Data, Non-confidential 2012 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Methanone, (2, 4-dihydroxyphenyl)phenyl-. National Production Volume: 31, 680 lb, yr., Non-confidential 2016 Chemical Data Reporting (CDR) information on the production and use of chemicals manufactured or imported into the United States. Chemical: Methanone, 4-dihydroxyphenyl)phenyl-:, Table: National Aggregate Production Volume (pounds) [Table#5461], U.S. Imports: (1979) No Data, (1981) 3.75X10+5 GRAMS (PRINCPL CUSTMS DISTS), U.S. Exports: (1979) No Data, General Manufacturing Information: Methanone, 4-dihydroxyphenyl)phenyl-: ACTIVE.
Category: Organic Chemicals.
Independent reference data for (2,4-dihydroxyphenyl)-phenyl-methanone (CAS 92092-63-2), compiled from public chemistry databases.
| CAS 号 | 92092-63-2 |
|---|---|
| PubChem CID | 8572 |
| 分子式 | C13H10O3 |
| IUPAC 名称 | (2,4-dihydroxyphenyl)-phenylmethanone |
| UNII（FDA） | LJ54R4Z029 |
| Molecular Weight | 214.22 |
|---|---|
| XLogP3 | 3.2 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 214.062994177 |
| Monoisotopic Mass | 214.062994177 |
| Topological Polar Surface Area | 57.5 |
| Heavy Atom Count | 16 |
| Boiling Point | BP: 194 °C at 1 mm Hg |
|---|---|
| Melting Point | 144 °C |
2,4-DIHYDROXYBENZOPHENONE; 131-56-6; Benzoresorcinol; Resbenzophenone; Inhibitor DHBP; Uvinul 400; Advastab 48; Uvistat 12; Quinsorb 010; Syntase 100; Methanone, (2,4-dihydroxyphenyl)phenyl-; Uvinol 400; Eastman Inhibitor DHPB; 4-Benzoyl resorcinol; Dastib 263; (2,4-Dihydroxyphenyl)phenylmethanone
| 法规与食品接触 | CIR / INCI: Cosmetic ingredients (Benzophenone-1) -> CIR (Cosmetic Ingredient Review) CIR / INCI: Uv absorber |
|---|---|
| GHS 通报统计 | 5.6% (109 / 1938) |
| GHS 通报统计 | 5.6% (109 / 1938) |
|---|---|
| 已通报的危害声明 | H315 (69.3%), H319 (93.6%), H335 (68.8%) |
(2,4-二羟基苯基)-苯基甲酮 · CAS 92092-63-2 · C13H10O3. UNII LJ54R4Z029. Boiling Point: BP: 194 °C at 1 mm Hg; Melting Point: 144 °C.
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.
中文页面: (2,4-二羟基苯基)-苯基甲酮