对氨基苯甲酸正丁酯（CAS 94-25-7）：分子式 C11H15NO2、分子量 193.24。
| CAS号 | 94-25-7 |
|---|---|
| 分子式 | C11H15NO2 |
| 分子量 | 193.24 |
| 熔点 | 136 °F (NTP, 1992) |
| 沸点 | 343 to 345 °F at 8 mmHg (NTP, 1992) |
| LogP | 2.87 |
| 应用领域 | Uses: Used as a local anesthetic and in burn treatment ointments and suntan preparations、[Hawley] Used essentially 100% as a local anesthetic、[HSDB]、MEDICATION、MEDICATION (VET)、Methods of Manufacturing: ESTERIFICATION OF P-NITROBENZOIC ACID WITH N-BUTYL ALCOHOL FOLLOWED BY REDUCTION WITH IRON FILINGS AND HYDROCHLORIC ACID、PREPARED BY ESTERIFYING P-NITROBENZOIC ACID WITH N-BUTYL ALCOHOL & REDUCING NITRO GROUP TO AMINO GROUP WITH IRON FILINGS & HCL.、Prepn: Brill、J. Am. Chem. Soic. 43、1322 (1921)、Adams、Volwiler、U.S. pat 1、440、652 (1923 to Abbott)、Brit. pat. 252、870、C.A. 17、1243 (1923)、C.A. 21、2478 (1927).、Produced by the esterification of 4-nitrobenzoyl chloride with n-butanol and reduction of the resulting nitroester.、Formulations、Preparations: ... MAY BE APPLIED AS DUSTING POWDERS、UNDIL OR DIL WITH STERILE TALC. THEY ARE SOL IN OIL & MAY BE INC IN OILY SOLN、OINTMENTS、& SUPPOSITORIES.、ANESTHETICS OF LOW SOLUBILITY、Grade: NF、Consumption Patterns: ESSENTIALLY 100% AS AN ANESTHETIC、U.S. Production: (1978) GREATER THAN 1.36X10+6 G (INCL PICRATE)、(1979) GREATER THAN 1.36X10+6 G (INCL PICRATE)、U.S. Imports: (1977) No Data、(1979) No Data、U.S. Exports: (1977) No Data、General Manufacturing Information: Benzoic acid、4-amino-、butyl ester: ACTIVE、Available in the United States as a surface anesthetic in the form of a picrate. |
登记用途：Uses: Used as a local anesthetic and in burn treatment ointments and suntan preparations、[Hawley] Used essentially 100% as a local anesthetic、[HSDB]、MEDICATION、MEDICATION (VET)、Methods of Manufacturing: ESTERIFICATION OF P-NITROBENZOIC ACID WITH N-BUTYL ALCOHOL FOLLOWED BY REDUCTION WITH IRON FILINGS AND HYDROCHLORIC ACID、PREPARED BY ESTERIFYING P-NITROBENZOIC ACID WITH N-BUTYL ALCOHOL & REDUCING NITRO GROUP TO AMINO GROUP WITH IRON FILINGS & HCL.、Prepn: Brill、J. Am. Chem. Soic. 43、1322 (1921)、Adams、Volwiler、U.S. pat 1、440、652 (1923 to Abbott)、Brit. pat. 252、870、C.A. 17、1243 (1923)、C.A. 21、2478 (1927).、Produced by the esterification of 4-nitrobenzoyl chloride with n-butanol and reduction of the resulting nitroester.、Formulations、Preparations: ... MAY BE APPLIED AS DUSTING POWDERS、UNDIL OR DIL WITH STERILE TALC. THEY ARE SOL IN OIL & MAY BE INC IN OILY SOLN、OINTMENTS、& SUPPOSITORIES.、ANESTHETICS OF LOW SOLUBILITY、Grade: NF、Consumption Patterns: ESSENTIALLY 100% AS AN ANESTHETIC、U.S. Production: (1978) GREATER THAN 1.36X10+6 G (INCL PICRATE)、(1979) GREATER THAN 1.36X10+6 G (INCL PICRATE)、U.S. Imports: (1977) No Data、(1979) No Data、U.S. Exports: (1977) No Data、General Manufacturing Information: Benzoic acid、4-amino-、butyl ester: ACTIVE、Available in the United States as a surface anesthetic in the form of a picrate.。
对氨基苯甲酸正丁酯 是一种化工化合物，登记 CAS 号为 94-25-7，分子式 C11H15NO2（分子量 193.24）。
登记 CAS 号：94-25-7
其分子式 C11H15NO2 由 11 个碳、15 个氢、1 个氮、2 个氧 组成。
别名/同义词：对氨基苯甲酸正丁酯 · n-Butyl-p-Aminobenzoate
对氨基苯甲酸正丁酯 的 CAS 登记号为 94-25-7。
分子式 C11H15NO2，分子量 193.24。
别名/同义词：对氨基苯甲酸正丁酯、n-Butyl-p-Aminobenzoate。
登记用途：Uses: Used as a local anesthetic and in burn treatment ointments and suntan preparations、[Hawley] Used essentially 100% as a local anesthetic、[HSDB]、MEDICATION、MEDICATION (VET)、Methods of Manufacturing: ESTERIFICATION OF P-NITROBENZOIC ACID WITH N-BUTYL ALCOHOL FOLLOWED BY REDUCTION WITH IRON FILINGS AND HYDROCHLORIC ACID、PREPARED BY ESTERIFYING P-NITROBENZOIC ACID WITH N-BUTYL ALCOHOL & REDUCING NITRO GROUP TO AMINO GROUP WITH IRON FILINGS & HCL.、Prepn: Brill、J. Am. Chem. Soic. 43、1322 (1921)、Adams、Volwiler、U.S. pat 1、440、652 (1923 to Abbott)、Brit. pat. 252、870、C.A. 17、1243 (1923)、C.A. 21、2478 (1927).、Produced by the esterification of 4-nitrobenzoyl chloride with n-butanol and reduction of the resulting nitroester.、Formulations、Preparations: ... MAY BE APPLIED AS DUSTING POWDERS、UNDIL OR DIL WITH STERILE TALC. THEY ARE SOL IN OIL & MAY BE INC IN OILY SOLN、OINTMENTS、& SUPPOSITORIES.、ANESTHETICS OF LOW SOLUBILITY、Grade: NF、Consumption Patterns: ESSENTIALLY 100% AS AN ANESTHETIC、U.S. Production: (1978) GREATER THAN 1.36X10+6 G (INCL PICRATE)、(1979) GREATER THAN 1.36X10+6 G (INCL PICRATE)、U.S. Imports: (1977) No Data、(1979) No Data、U.S. Exports: (1977) No Data、General Manufacturing Information: Benzoic acid、4-amino-、butyl ester: ACTIVE、Available in the United States as a surface anesthetic in the form of a picrate.。
对氨基苯甲酸正丁酯（CAS 94-25-7）的独立参考数据，整理自公开化学数据库。
| CAS Registry Number | 94-25-7 |
|---|---|
| PubChem CID | 2482 |
| Molecular formula | C11H15NO2 |
| IUPAC name | butyl 4-aminobenzoate |
| UNII (FDA) | EFW857872Q |
| Molecular Weight | 193.24 |
|---|---|
| XLogP3 | 2.9 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Exact Mass | 193.110278721 |
| Monoisotopic Mass | 193.110278721 |
| Topological Polar Surface Area | 52.3 |
| Heavy Atom Count | 14 |
| Boiling Point | 343 to 345 °F at 8 mmHg (NTP, 1992) |
|---|---|
| Boiling Point | 173.5 |
| Boiling Point | 173-174 °C @ 8 mm Hg |
| Melting Point | 136 °F (NTP, 1992) |
| Melting Point | 58 |
| Melting Point | 58 °C |
| Solubility | 140 |
| Solubility | In water, 3.35X10+2 mg/l @ 25 °C |
| Vapor Pressure | 0.000299 [mmHg] |
| LogP | 2.87 |
Butyl 4-aminobenzoate; butamben; 94-25-7; Butesine; Butoform; Butyl aminobenzoate; Butylcaine; Planoform; Scuroform; Scuroforme; 4-(Butoxycarbonyl)aniline; Butyl keloform; Benzoic acid, 4-amino-, butyl ester; N-Butyl p-aminobenzoate; p-Aminobenzoic acid butyl ester; 4-Aminobenzoic acid butyl ester
| Reported hazard statements | H315 (100%), H317 (95.3%), H319 (100%), H335 (95.3%) |
|---|
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
H317 (95.3%): May cause an allergic skin reaction [Warning Sensitization, Skin]
n-Butyl-p-Aminobenzoate · CAS 94-25-7 · C11H15NO2. UNII EFW857872Q. Boiling Point: 343 to 345 °F at 8 mmHg (NTP, 1992); Boiling Point: 173.5; Boiling Point: 173-174 °C @ 8 mm Hg.
数据来源：PubChem / Wikidata；与随货 COA 不一致时以 COA 为准。
English page: n-Butyl-p-Aminobenzoate