右氯苯那敏（CAS 25523-97-1）：分子式 C16H19ClN2、分子量 274.79。
| CAS号 | 25523-97-1 |
|---|---|
| 分子式 | C16H19ClN2 |
| 分子量 | 274.79 |
| 沸点 | 142 °C @ 1.0 mm Hg /Racemate/ |
| LogP | 3.4 |
| 应用领域 | Uses: ANTIHISTAMINE FOR ALLERGIC & VASOMOTOR RHINITIS (MALEATE)、ANTIHISTAMINE FOR MILD URTICARIA AND ANGIOEDEMA (MALEATE)、ANTIHISTAMINE FOR INSECT BITE REACTIONS (MALEATE)、ANTIHISTAMINE FOR PRURITUS OF ALLERGIC REACTIONS、MALEATE、Used used in the prevention of the symptoms of allergic conditions such as rhinitis、urticaria、allergy、common cold、asthma and hay fever.、Methods of Manufacturing: RACEMIC CHLORPHENIRAMINE...IS RESOLVED WITH AID OF D-PHENYLSUCCINIC ACID. D-ENANTIOMORPH OF BASE IS THEN LIBERATED FROM ITS D-PHENYLSUCCINATE BY TREATMENT WITH SODIUM HYDROXIDE & REACTED WITH EQUIMOLAR PORTION OF MALEIC ACID.、CONDENSATION OF 2-(P-CHLORO-ALPHA-(2-CHLOROETHYL)BENZYL)PYRIDINE WITH DIMETHYLAMINE TO PRODUCE RACEMIC CHLORPHENIRAMINE、SEPARATION OF DEXTRO ISOMER USING D-PHENYLSUCCINIC ACID、FOLLOWED BY SEQUENTIAL TREATMENT WITH SODIUM HYDROXIDE & MALEIC ACID (MALEATE)、Formulations、Preparations: SYRUP NF: 2 MG、5 ML、TABLETS NF: 2 MG、Chlo-amine、Fortamine、Isomerine、Phenamin、Phendextro、Polaramine、Polaronil、Sensidyn、d-Form maleate、Consumption Patterns: ESSENTIALLY 100% AS AN ANTIHISTAMINE (MALEATE、1976)、U.S. Production: (1972) GREATER THAN 4.54X10+5 G、(1975) GREATER THAN 4.54X10+5 G |
登记用途：Uses: ANTIHISTAMINE FOR ALLERGIC & VASOMOTOR RHINITIS (MALEATE)、ANTIHISTAMINE FOR MILD URTICARIA AND ANGIOEDEMA (MALEATE)、ANTIHISTAMINE FOR INSECT BITE REACTIONS (MALEATE)、ANTIHISTAMINE FOR PRURITUS OF ALLERGIC REACTIONS、MALEATE、Used used in the prevention of the symptoms of allergic conditions such as rhinitis、urticaria、allergy、common cold、asthma and hay fever.、Methods of Manufacturing: RACEMIC CHLORPHENIRAMINE...IS RESOLVED WITH AID OF D-PHENYLSUCCINIC ACID. D-ENANTIOMORPH OF BASE IS THEN LIBERATED FROM ITS D-PHENYLSUCCINATE BY TREATMENT WITH SODIUM HYDROXIDE & REACTED WITH EQUIMOLAR PORTION OF MALEIC ACID.、CONDENSATION OF 2-(P-CHLORO-ALPHA-(2-CHLOROETHYL)BENZYL)PYRIDINE WITH DIMETHYLAMINE TO PRODUCE RACEMIC CHLORPHENIRAMINE、SEPARATION OF DEXTRO ISOMER USING D-PHENYLSUCCINIC ACID、FOLLOWED BY SEQUENTIAL TREATMENT WITH SODIUM HYDROXIDE & MALEIC ACID (MALEATE)、Formulations、Preparations: SYRUP NF: 2 MG、5 ML、TABLETS NF: 2 MG、Chlo-amine、Fortamine、Isomerine、Phenamin、Phendextro、Polaramine、Polaronil、Sensidyn、d-Form maleate、Consumption Patterns: ESSENTIALLY 100% AS AN ANTIHISTAMINE (MALEATE、1976)、U.S. Production: (1972) GREATER THAN 4.54X10+5 G、(1975) GREATER THAN 4.54X10+5 G。
右氯苯那敏 是一种化工化合物，登记 CAS 号为 25523-97-1，分子式 C16H19ClN2（分子量 274.79）。
登记 CAS 号：25523-97-1
其分子式 C16H19ClN2 由 16 个碳、19 个氢、1 个氯、2 个氮 组成。
别名/同义词：右氯苯那敏 · Dexchlorpheniramine
右氯苯那敏 的 CAS 登记号为 25523-97-1。
分子式 C16H19ClN2，分子量 274.79。
别名/同义词：右氯苯那敏、Dexchlorpheniramine。
登记用途：Uses: ANTIHISTAMINE FOR ALLERGIC & VASOMOTOR RHINITIS (MALEATE)、ANTIHISTAMINE FOR MILD URTICARIA AND ANGIOEDEMA (MALEATE)、ANTIHISTAMINE FOR INSECT BITE REACTIONS (MALEATE)、ANTIHISTAMINE FOR PRURITUS OF ALLERGIC REACTIONS、MALEATE、Used used in the prevention of the symptoms of allergic conditions such as rhinitis、urticaria、allergy、common cold、asthma and hay fever.、Methods of Manufacturing: RACEMIC CHLORPHENIRAMINE...IS RESOLVED WITH AID OF D-PHENYLSUCCINIC ACID. D-ENANTIOMORPH OF BASE IS THEN LIBERATED FROM ITS D-PHENYLSUCCINATE BY TREATMENT WITH SODIUM HYDROXIDE & REACTED WITH EQUIMOLAR PORTION OF MALEIC ACID.、CONDENSATION OF 2-(P-CHLORO-ALPHA-(2-CHLOROETHYL)BENZYL)PYRIDINE WITH DIMETHYLAMINE TO PRODUCE RACEMIC CHLORPHENIRAMINE、SEPARATION OF DEXTRO ISOMER USING D-PHENYLSUCCINIC ACID、FOLLOWED BY SEQUENTIAL TREATMENT WITH SODIUM HYDROXIDE & MALEIC ACID (MALEATE)、Formulations、Preparations: SYRUP NF: 2 MG、5 ML、TABLETS NF: 2 MG、Chlo-amine、Fortamine、Isomerine、Phenamin、Phendextro、Polaramine、Polaronil、Sensidyn、d-Form maleate、Consumption Patterns: ESSENTIALLY 100% AS AN ANTIHISTAMINE (MALEATE、1976)、U.S. Production: (1972) GREATER THAN 4.54X10+5 G、(1975) GREATER THAN 4.54X10+5 G。
右氯苯那敏（CAS 25523-97-1）的独立参考数据，整理自公开化学数据库。
| CAS Registry Number | 25523-97-1 |
|---|---|
| PubChem CID | 33036 |
| Molecular formula | C16H19ClN2 |
| IUPAC name | (3S)-3-(4-chlorophenyl)-N,N-dimethyl-3-pyridin-2-ylpropan-1-amine |
| UNII (FDA) | 3Q9Q0B929N |
| Molecular Weight | 274.79 |
|---|---|
| XLogP3 | 3.4 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 5 |
| Exact Mass | 274.1236763 |
| Monoisotopic Mass | 274.1236763 |
| Topological Polar Surface Area | 16.1 |
| Heavy Atom Count | 19 |
| Boiling Point | 142 °C @ 1.0 mm Hg /Racemate/ |
|---|
DEXCHLORPHENIRAMINE; 25523-97-1; D-Chlorpheniramine; (+)-Chlorpheniramine; Chlo-amine; Phendextro; Dexclorfeniramina; Dapriton; Fortamine; Isomerine; Polaramin; Dexchlorpheniraminum; Chlorpheniramine, d-; Chlorphenamine, (s)-; Chlorpheniramine, (s)-; (3S)-3-(4-chlorophenyl)-N,N-dimethyl-3-pyridin-2-ylpropan-1-amine
Dexchlorpheniramine · CAS 25523-97-1 · C16H19ClN2. UNII 3Q9Q0B929N. Boiling Point: 142 °C @ 1.0 mm Hg /Racemate/.
数据来源：PubChem / Wikidata；与随货 COA 不一致时以 COA 为准。
English page: Dexchlorpheniramine