1-나프톨
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1-나프톨 속성
- 녹는점
- 94-96 °C(lit.)
- 끓는 점
- 278-280 °C(lit.)
- 밀도
- 1.224
- 증기 밀도
- 4.5 (120 °C, vs air)
- 증기압
- 1 mm Hg ( 94 °C)
- 굴절률
- 1.6224
- 인화점
- 125 °C
- 저장 조건
- Store below +30°C.
- 용해도
- 벤젠, 클로로포름, 에테르 및 에탄올에 용해됩니다.
- 산도 계수 (pKa)
- 9.34(at 25℃)
- 물리적 상태
- 플레이크 크리스탈
- 색상
- 흰색에서 황백색까지
- 냄새
- 약간의 페놀 냄새
- 폭발한계
- 5%
- 수용성
- 436.7mg/L(25 ºC)
- 최대 파장(λmax)
- 324nm(MeOH)(lit.)
- 감도
- Air & Light Sensitive
- Merck
- 14,6383
- BRN
- 1817321
- 안정성
- 안정적이지만 공기와 빛에 민감합니다. 불활성 가스하에 보관하십시오. 강염기, 강산화제와 호환되지 않습니다.
- InChIKey
- KJCVRFUGPWSIIH-UHFFFAOYSA-N
- LogP
- 2.84 at 25℃
- CAS 데이터베이스
- 90-15-3(CAS DataBase Reference)
안전
- 위험 및 안전 성명
- 위험 및 사전주의 사항 (GHS)
위험품 표기 | Xn,N | ||
---|---|---|---|
위험 카페고리 넘버 | 21/22-37/38-41-51/53 | ||
안전지침서 | 22-26-37/39-2-61 | ||
유엔번호(UN No.) | UN 2811 6.1/PG 3 | ||
WGK 독일 | 1 | ||
RTECS 번호 | QL2800000 | ||
F 고인화성물질 | 8-23 | ||
자연 발화 온도 | 510 °C | ||
TSCA | Yes | ||
위험 등급 | 6.1 | ||
포장분류 | III | ||
HS 번호 | 29071510 | ||
유해 물질 데이터 | 90-15-3(Hazardous Substances Data) | ||
독성 | LD50 orally in Rabbit: 1870 mg/kg LD50 dermal Rabbit 880 mg/kg | ||
기존화학 물질 | KE-25703 |
1-나프톨 C화학적 특성, 용도, 생산
개요
1-Naphthol, or α-naphthol, is a fluorescent organic compound with the formula C10H7OH. It is a white solid. It is an isomer of 2-naphthol differing by the location of the hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol, with the hydroxyl group being more reactive than in the phenols. Both isomers are soluble in simple alcohols, ethers, and chloroform. They are precursors to a variety of useful compounds. Naphthols (both 1 and 2 isomers) are used as biomarkers for livestock and humans exposed to polycyclic aromatic hydrocarbons.α-naphtol, combined with epichlorhydrine and sodium hydroxide to form alpha-naphtyl glycidyl ether, caused sensitization in one of three workers in a chemical plant.
화학적 성질
Pale grey to brown solid with an unpleasant phenol odour. Darkens in the presence of light. Evaporates with water vapour. Soluble in ethanol, ether, benzene, chloroform and alkali solutions, insoluble in water. Precipitates violet when exposed to ferric chloride. 1-Naphthol [90-15-3] a-naphthol, 1- naphthalenol, 1-hydroxynaphthalene, C10H8O, Mr 144.16, forms colorless prisms (from toluene) which darken on exposure to air or light. The compound is steam volatile and sublimable. 1-Naphthol is reduced by sodium in liquid ammonia to give 5,6,7,8-tetrahydro-1-naphthol and is oxidized by NaOCl – FeCl3 or I2–KI to give a violet color. It is chlorinated by phosphorus pentachloride at 150℃ to give 1-chloronaphthalene, by sulfuryl chloride to give 4- chloro-1-naphthol, or by Cl2–CH3COOH to give 2,4-dichloro-1-naphthol. Similarly bromine forms 2,4-dibromo-1-naphthol, and this reaction may be used quantitatively for titration. Nitration of 1-naphthol gives complex mixtures. The crude 2,4-dinitro derivative was used in the mid-1800s as an acid yellow dye comparable to picric acid. Sulfonation at 50℃ readily yields 1-naphthol-2,4-disulfonic acid. Nitrous acid gives mainly the 2-nitroso derivative, contaminated with the 4-nitroso isomer.용도
1-Naphthol is used as a precursor in the manufacturing of various azo dyes and pharmaceuticals such as nadolol. It is used as biomarkers. It is used in analytical chemistry as Molisch's reagent (1-naphthol dissolved in ethanol) for checking the presence of carbohydrates. It plays an essential role with sodium hypobromite to detect the presence of arginine in proteins, which is called as Sakaguchi test.제조 방법
2-Isopropylnaphthalene can be used to synthesize 1-naphthol by oxidation via the hydroperoxide (Hock synthesis).Historically 1-naphthol was produced via caustic fusion of naphthalene-1-sulfonic acid, but this was superseded by the I.G. Farbenindustrie process involving hydrolysis of 1-naphthylamine with aqueous 22 % sulfuric acid at 200°C under pressure in a lead-lined autoclave. To obtain a purer product, Union Carbide developed a process based on catalytic oxidation of tetralin to 1-tetralol and 1-tetralone followed by dehydrogenation. The two-stage catalytic process is claimed to give an overall yield of 72% 1-naphthol, with an overall efficiency of 97%.
정의
ChEBI: 1-naphthol is a naphthol carrying a hydroxy group at position 1. It has a role as a genotoxin and a human xenobiotic metabolite.주요 응용
1-Naphthol is a hydroxyl-aromatic compound. It has been used as a prooxidant to analyze its ability to induce hemolysis in a zebrafish G6PD (glucose-6-phosphate dehydrogenase) deficiency model.일반 설명
1-Naphthol, a metabolite of carbaryl and naphthanlene. It is formed by spontaneous reaction from (1R, 2S)-Naphthalene epoxide followed to form 1, 4-Dihydroxynaphthalene.위험도
Toxic by ingestion and skin absorption.색상 색인 번호
1-Naphthol can be used in dye manufacture and is classified as a hair dye. Combined with epichlorhydrin and NaOH to form alpha-naphthyl glycidyl ether, it caused sensitization in one of three workers in a chemical plant.Safety Profile
Poison by ingestion and intraperitoneal routes. Moderately toxic by skin contact. An experimental teratogen. Experimental reproductive effects. A severe eye and skin irritant. Mutation data reported. Ingestion of large amounts can cause nephritis, vomiting, diarrhea, circulatory collapse, anemia, convulsions, and death. Can cause kidney irritation and injury to cornea and lens of the eye. Combustible when exposed to heat or flame. When heated to decomposition it emits acrid smoke and irritating fumes.Synthesis
To a 10 mL pressure vessel, aryl halide (1.00 mmol), copper (I) oxide (0.05 mol), ligand (0.05 mol), 3 M sodium hydroxide (2 mL), and organic solvent (2 mL) were added. The reaction mixture was irradiated at 160 °C for 10 min with strong stirring. The reaction mixture was allowed to cool to room temperature. The reaction mixture was filtered through a plug of celite in a fritted filter funnel and washed with ethyl acetate. The product was extracted using 30 mL of ethyl acetate for three times. The organic extract is washed three times with 10 mL water and two times with 10 mL of brine. The combined organic phases were dried over anhydrous MgSO4 and the solvent was removed under reduced pressure to afford 1-naphthol.Purification Methods
Sublime 1-naphthol, then crystallise it from aqueous MeOH (charcoal), aqueous 25% or 50% EtOH, *C6H6, cyclohexane, heptane, CCl4 or H2O. Dry it over P2O5 in vacuo. The 4-nitrobenzoate has m 143o (from EtOH). [Shizuka et al. J Am Chem Soc 107 7816 1985, Beilstein 8 H 596, 6 IV 4208.]1-나프톨 준비 용품 및 원자재
원자재
1-클로로나프탈렌
dilute sulphuric acid
나프탈렌
테트라히드로나프탈렌
2-Ethylnitrobenzene
암모늄 이황산염
Naphthalene-2-sulfonic acid
1-나프틸아민
몰리브덴산(MOLYBDIC ACID)
1-나프탈렌설폰산, 테크니칼
황산
준비 용품
1-NAPHTHOXYACETIC ACID
fluorescent whitening agent OM
6-메톡시-알파-메틸나프탈렌-1-아세트알데히드
1-에테닐-1,2,3,4-테트라히드로-6-메톡시-1-나프탈레놀
17-Ethinyl-3,17-dihydroxy-18-methylestra-2,5(10)-diene3-methylether
2-(1-Naphthalenyloxy)propanoic acid
1-에톡시나프탈렌
1-니트로소-2-나프톨
플라비아산
C.I. 색소 적색 68
2-에톡시나프탈렌-1-카르보닐클로라이드
1-(6-하이드록시-2-나프틸)에탄-1-온
2-BROMO-1-(6-METHOXY-2-NAPHTHALENYL)-1-PROPANONE
13-Ethyl-17-hydroxy-18,19-dinorpregn-5(10)-en-20-yn-3-one
3-Methoxy-18-methylestra-1,3,5(10),8-tetraen-17-ethylene ketal
N,N'-디-2나프틸-p-페닐렌디아민
2-[(1-나프틸옥시)메틸]옥시란
에탄올, 2-((2-아미노에틸)아미노)-
적색205호
4-Amino-1-naphthol hydrochloride
에리오크롬 블랙 T
에틸3-(6-메톡시-2-나프틸)-3-메틸글리시데이트
메틸3-(6-메톡시-2-나프틸)-3-메틸글리시데이트
synthetic tanning agent No.3
1-Hydroxy-2-naphthoic acid
5,8-디히드로나프톨
17-Ethinyl-17-hydroxy-18-methylestra-5(10),9(11)-dien-3-one-3-ethylene ketal
1,6-Dibromo-2-naphthol
Mordant Black 3
산 적색 1
2-니트로소-1-나프톨
1,4-나프토퀴논
1,6-디브로모-2-메톡시나프탈렌
3-Methoxy-18-methylestra-2,5(10)dien-17-one 17-ethylene ketal
나프로아닐리드
6'-메톡시-2'-프로피오노나프톤
1-나프틸클로로포메이트
O-2-나프틸클로로티오포르메이트
17-Ethynyl-18-methylestra-5(10),9(11)-dien-17-ol-3-one
나프로P아마이드
1-나프톨 공급 업체
글로벌( 818)공급 업체
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Changzhou waston chemical technology Co.,Ltd | +86-051985861892 +8618112881323 |
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Auschemicals Pty Ltd | +61406202619 |
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Guangzhou Tosun Pharmaceutical Limited | +8618922120635 |
sales@toref-standards.com | China | 998 | 58 |
Jinan Finer Chemical Co., Ltd | +86-531-88989536 +86-15508631887 |
sales@finerchem.com | China | 2964 | 58 |
Hebei Chuanghai Biotechnology Co,.LTD | +86-13131129325 |
sales1@chuanghaibio.com | China | 5893 | 58 |
Hebei Saisier Technology Co., LTD | +86-18400010335 +86-18034520335 |
admin@hbsaisier.cn | China | 1015 | 58 |
Hebei Longbang Technology Co., LTD | +86-18633929156 +86-18633929156 |
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Hebei Mojin Biotechnology Co.,Ltd | +86-15028179902 |
angelia@hbmojin.com | China | 1179 | 58 |
HebeiShuoshengImportandExportco.,Ltd | +86-18532138899 +86-18532138899 |
L18532138899@163.com | China | 939 | 58 |
Capot Chemical Co.,Ltd. | +86-(0)57185586718 +86-13336195806 |
sales@capot.com | China | 29791 | 60 |