萘胺（CAS 25168-10-9）：分子式 C10H9N、分子量 143.18。
| CAS号 | 25168-10-9 |
|---|---|
| 分子式 | C10H9N |
| 分子量 | 143.18 |
| 熔点 | 122 °F (NTP, 1992) |
| 沸点 | 574 °F at 760 mmHg (NTP, 1992) |
| LogP | 2.2 |
| 应用领域 | Uses: Former uses included: a chemical intermediate for the synthesis of dyes、rubber antioxidants、and pesticides、[HSDB]、See 29CFR1910.1003 (Code of Federal Regulations}、Toning prints made with cerium salts.、Chemical intermediate for dyes、eg、azoic diazo component、chemical intermediate for azo dye coupling agents、for n-1-naphthylphthalmic acid herbicide、for n-phenyl-1-naphthylamine rubber antioxidant、for an imidazoline adrenergic agent、chemical intermediate for 1-naphthylthiourea rodenticide and for a fluoroacetamide miticide.、SRP60: Former、1-Naphthylamine is used as an intermediate in the synthesis of dyes、antioxidants、herbicides、some drugs、and other chemicals.、In agricultural chemicals、Methods of Manufacturing: Reduction of 1-nitronaphthalene by catalytic hydrogenation with a nickel catalyst ... .、Prepared by reducing alpha-nitronaphthalene with iron and hydrochloric acid.、Naphthalene is nitrated with H2SO4-HNO3 at 50-60 °C. The crude product (mp 52 °C) is separated、washed with hot water、and further purified by crystallization or sweating (draining of the lower melting point isomer) to remove 2-nitronaphthalene (3%) and traces of 2、4-dinitronaphthalene. purified 1-nitronaphthalene was traditionally reduced with iron in boiling dilute hydrochloric acid、but modern plants use hydrogenation with nickel catalyst. The 1-naphthylamine produced is further purified by distillation under vacuum. The content of 2-naphthylamine in the commercial product is specified at less than 10 ppm.、Impurities: Most commercial 1-naphthylamine ... contains 4-10% of 2-naphthylamine if synthesized by methods used in previous decades. Modern production methods give rise to a max of 0.5%.、U.S. Production: (1978) PROBABLY GREATER THAN 2.27X10+6 G、(1982) PROBABLY GREATER THAN 2.27X10+6 G、(1985) Data not reported、U.S. Imports: (1977) 5.16X10+7 G (PRINCPL CUSTMS DISTS)、(1982) 9.91X10+7 G (PRINCPL CUSTMS DISTS)、General Manufacturing Information: 1-Naphthalenamine: ACTIVE |
登记用途：Uses: Former uses included: a chemical intermediate for the synthesis of dyes、rubber antioxidants、and pesticides、[HSDB]、See 29CFR1910.1003 (Code of Federal Regulations}、Toning prints made with cerium salts.、Chemical intermediate for dyes、eg、azoic diazo component、chemical intermediate for azo dye coupling agents、for n-1-naphthylphthalmic acid herbicide、for n-phenyl-1-naphthylamine rubber antioxidant、for an imidazoline adrenergic agent、chemical intermediate for 1-naphthylthiourea rodenticide and for a fluoroacetamide miticide.、SRP60: Former、1-Naphthylamine is used as an intermediate in the synthesis of dyes、antioxidants、herbicides、some drugs、and other chemicals.、In agricultural chemicals、Methods of Manufacturing: Reduction of 1-nitronaphthalene by catalytic hydrogenation with a nickel catalyst ... .、Prepared by reducing alpha-nitronaphthalene with iron and hydrochloric acid.、Naphthalene is nitrated with H2SO4-HNO3 at 50-60 °C. The crude product (mp 52 °C) is separated、washed with hot water、and further purified by crystallization or sweating (draining of the lower melting point isomer) to remove 2-nitronaphthalene (3%) and traces of 2、4-dinitronaphthalene. purified 1-nitronaphthalene was traditionally reduced with iron in boiling dilute hydrochloric acid、but modern plants use hydrogenation with nickel catalyst. The 1-naphthylamine produced is further purified by distillation under vacuum. The content of 2-naphthylamine in the commercial product is specified at less than 10 ppm.、Impurities: Most commercial 1-naphthylamine ... contains 4-10% of 2-naphthylamine if synthesized by methods used in previous decades. Modern production methods give rise to a max of 0.5%.、U.S. Production: (1978) PROBABLY GREATER THAN 2.27X10+6 G、(1982) PROBABLY GREATER THAN 2.27X10+6 G、(1985) Data not reported、U.S. Imports: (1977) 5.16X10+7 G (PRINCPL CUSTMS DISTS)、(1982) 9.91X10+7 G (PRINCPL CUSTMS DISTS)、General Manufacturing Information: 1-Naphthalenamine: ACTIVE。
萘胺 是一种化工化合物，登记 CAS 号为 25168-10-9，分子式 C10H9N（分子量 143.18）。
登记 CAS 号：25168-10-9
其分子式 C10H9N 由 10 个碳、9 个氢、1 个氮 组成。
别名/同义词：萘胺 · Naphthylamine
萘胺 的 CAS 登记号为 25168-10-9。
分子式 C10H9N，分子量 143.18。
别名/同义词：萘胺、Naphthylamine。
登记用途：Uses: Former uses included: a chemical intermediate for the synthesis of dyes、rubber antioxidants、and pesticides、[HSDB]、See 29CFR1910.1003 (Code of Federal Regulations}、Toning prints made with cerium salts.、Chemical intermediate for dyes、eg、azoic diazo component、chemical intermediate for azo dye coupling agents、for n-1-naphthylphthalmic acid herbicide、for n-phenyl-1-naphthylamine rubber antioxidant、for an imidazoline adrenergic agent、chemical intermediate for 1-naphthylthiourea rodenticide and for a fluoroacetamide miticide.、SRP60: Former、1-Naphthylamine is used as an intermediate in the synthesis of dyes、antioxidants、herbicides、some drugs、and other chemicals.、In agricultural chemicals、Methods of Manufacturing: Reduction of 1-nitronaphthalene by catalytic hydrogenation with a nickel catalyst ... .、Prepared by reducing alpha-nitronaphthalene with iron and hydrochloric acid.、Naphthalene is nitrated with H2SO4-HNO3 at 50-60 °C. The crude product (mp 52 °C) is separated、washed with hot water、and further purified by crystallization or sweating (draining of the lower melting point isomer) to remove 2-nitronaphthalene (3%) and traces of 2、4-dinitronaphthalene. purified 1-nitronaphthalene was traditionally reduced with iron in boiling dilute hydrochloric acid、but modern plants use hydrogenation with nickel catalyst. The 1-naphthylamine produced is further purified by distillation under vacuum. The content of 2-naphthylamine in the commercial product is specified at less than 10 ppm.、Impurities: Most commercial 1-naphthylamine ... contains 4-10% of 2-naphthylamine if synthesized by methods used in previous decades. Modern production methods give rise to a max of 0.5%.、U.S. Production: (1978) PROBABLY GREATER THAN 2.27X10+6 G、(1982) PROBABLY GREATER THAN 2.27X10+6 G、(1985) Data not reported、U.S. Imports: (1977) 5.16X10+7 G (PRINCPL CUSTMS DISTS)、(1982) 9.91X10+7 G (PRINCPL CUSTMS DISTS)、General Manufacturing Information: 1-Naphthalenamine: ACTIVE。
萘胺（CAS 25168-10-9）的独立参考数据，整理自公开化学数据库。
| CAS Registry Number | 25168-10-9 |
|---|---|
| PubChem CID | 8640 |
| Molecular formula | C10H9N |
| IUPAC name | naphthalen-1-amine |
| UNII (FDA) | 9753I242R5 |
| Molecular Weight | 143.18 |
|---|---|
| XLogP3 | 2.2 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 143.073499291 |
| Monoisotopic Mass | 143.073499291 |
| Topological Polar Surface Area | 26 |
| Heavy Atom Count | 11 |
| Boiling Point | 574 °F at 760 mmHg (NTP, 1992) |
|---|---|
| Boiling Point | 300.7 °C |
| Boiling Point | 300.8 °C |
| Boiling Point | 573 °F |
| Boiling Point | 300.7 °C @760 [mm Hg] |
| Melting Point | 122 °F (NTP, 1992) |
| Melting Point | 49.2 °C |
| Melting Point | 50.0 °C |
| Melting Point | 122 °F |
| Flash Point | 315 °F (NTP, 1992) |
1-NAPHTHYLAMINE; 1-Aminonaphthalene; 134-32-7; naphthalen-1-amine; 1-Naphthalenamine; alpha-Naphthylamine; Naphthalidine; Naphthalen-1-ylamine; Fast Garnet Base B; Naphthalidam; 1-Naphthalamine; 1-Naphthylamin; 1-Naftilamina; alpha-Aminonaphthalene; Alfanaftilamina; Fast Garnet B Base
| Regulatory & Food Contact | FDA Inventory of Food Contact Substances Listed in 21 CFR: FCS |
|---|
| Reported hazard statements | H302, H411, H310 (13.6%), H311 (37.5%), H317 (37.5%), H320, H371 |
|---|
H302: Harmful if swallowed [Warning Acute toxicity, oral]
H411: Toxic to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard]
Naphthylamine · CAS 25168-10-9 · C10H9N. UNII 9753I242R5. Boiling Point: 574 °F at 760 mmHg (NTP, 1992); Boiling Point: 300.7 °C; Boiling Point: 300.8 °C.
数据来源：PubChem / Wikidata；与随货 COA 不一致时以 COA 为准。
English page: Naphthylamine