- 1,3-DIHYDROXYNAPHTHALENE
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- $15.00 / 1KG
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2021-07-13
- CAS:132-86-5
- Min. Order: 1KG
- Purity: 99%+ HPLC
- Supply Ability: Monthly supply of 1 ton
- 1,3-DIHYDROXYNAPHTHALENE
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- $15.00 / 1KG
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2021-07-10
- CAS:132-86-5
- Min. Order: 1KG
- Purity: 99%+ HPLC
- Supply Ability: Monthly supply of 1 ton
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| 1,3-DIHYDROXYNAPHTHALENE Basic information |
Product Name: | 1,3-DIHYDROXYNAPHTHALENE | Synonyms: | 3-Hydroxybenzocyclohexadien-1-one;Naphthalenediol-(1,3);Naphthoresorcin;NAPHTHORESORCINE;NaphthoresorcinolGr;NaphthoresorcinolGr-(1,3-DihydroxyNaphthalene);1,3-Dihydroxynaphthalene, 99+%;1,3-Dioxynaphthalene | CAS: | 132-86-5 | MF: | C10H8O2 | MW: | 160.17 | EINECS: | 205-079-7 | Product Categories: | Industrial/Fine Chemicals | Mol File: | 132-86-5.mol | ![1,3-DIHYDROXYNAPHTHALENE Structure](CAS/GIF/132-86-5.gif) |
| 1,3-DIHYDROXYNAPHTHALENE Chemical Properties |
Melting point | 123-125 °C(lit.) | Boiling point | 246.06°C (rough estimate) | density | 1.0924 (rough estimate) | refractive index | 1.5418 (estimate) | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | solubility | ethanol: soluble50mg/mL | pka | 9.15±0.40(Predicted) | form | crystalline | color | white to tan | Water Solubility | Soluble in ethanol (50 mg/ml), and water. | Sensitive | Light Sensitive | Merck | 14,6396 | BRN | 2044002 | CAS DataBase Reference | 132-86-5(CAS DataBase Reference) | EPA Substance Registry System | 1,3-Naphthalenediol (132-86-5) |
Hazard Codes | Xi | Risk Statements | 36/37/38-22 | Safety Statements | 26-37/39 | WGK Germany | 3 | RTECS | QJ4725000 | F | 8-9-23 | TSCA | Yes | HS Code | 29029090 | Toxicity | mouse,LD50,intraperitoneal,200mg/kg (200mg/kg),National Technical Information Service. Vol. AD691-490, |
| 1,3-DIHYDROXYNAPHTHALENE Usage And Synthesis |
Chemical Properties | orange-pink to brown crystalline powder. 1,3-Naphthalenediol [132-86-5], naphthoresorcinol, mp 124℃, is synthesized by hydrolysis of 1,3-naphthalenediamine with sulfuric acid; by heating 1-amino-3-hydroxy-naphthalene-4-sulfonic acid with acid; or by cyclization of ethyl phenylacetoacetate. It is used as an analytical reagent for sugars and glucuronic acid in urine. It is oxidized in alkaline solution to 2-hydroxy-1,4-naphthoquinone and reacts with ammonia at 140℃ to give 3-amino-1- naphthol and 1,3-naphthalenediamine. | Uses | Reagent for sugars, oils, and for glucuronic acid in urine: Forsyth, Nature 161, 239 (1948); Heyns, Kelch, Z. Anal. Chem. 139, 339 (1953). | Uses | 1,3-Naphthalenediol is a derivative of naphthalene (N345600) and may have antibacterial activity against oral bacteria.Dyes and metabolites. |
| 1,3-DIHYDROXYNAPHTHALENE Preparation Products And Raw materials |
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