(2,4-二羟基苯基)-苯基甲酮（CAS 92092-63-2）：分子式 C13H10O3、分子量 214.22。
| CAS号 | 92092-63-2 |
|---|---|
| 分子式 | C13H10O3 |
| 分子量 | 214.22 |
| 熔点 | 144 °C |
| 沸点 | BP: 194 °C at 1 mm Hg |
| LogP | 3.2 |
| 应用领域 | 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 |
登记用途：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。
(2,4-二羟基苯基)-苯基甲酮 是一种化工化合物，登记 CAS 号为 92092-63-2，分子式 C13H10O3（分子量 214.22）。
登记 CAS 号：92092-63-2
其分子式 C13H10O3 由 13 个碳、10 个氢、3 个氧 组成。
别名/同义词：(2,4-二羟基苯基)-苯基甲酮 · (2,4-dihydroxyphenyl)-phenyl-methanone
(2,4-二羟基苯基)-苯基甲酮 的 CAS 登记号为 92092-63-2。
分子式 C13H10O3，分子量 214.22。
别名/同义词：(2,4-二羟基苯基)-苯基甲酮、(2,4-dihydroxyphenyl)-phenyl-methanone。
登记用途：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。
(2,4-二羟基苯基)-苯基甲酮（CAS 92092-63-2）的独立参考数据，整理自公开化学数据库。
| 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.
数据来源：PubChem / Wikidata；与随货 COA 不一致时以 COA 为准。
English page: (2,4-dihydroxyphenyl)-phenyl-methanone