- 2,2-Biphenol
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- $150.00 / 1kg
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2025-04-25
- CAS:1806-29-7
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 500kg
- biphenyl-2,2'-diol
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- $10.00 / 1KG
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2025-04-23
- CAS:1806-29-7
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 10 mt
- 2,2-biphenol
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- $0.00 / 25kg
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2025-04-15
- CAS:1806-29-7
- Min. Order: 25kg
- Purity: 97.0%~102.0%
- Supply Ability: 10tons
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| 2,2'-Biphenol Basic information |
Product Name: | 2,2'-Biphenol | Synonyms: | Orthodiphenol;2,2'-Biphenol,99%;2,2'-Dihydroxybiphenyl,99%;2,2’-Biphenol (2,2’-Dihydroxybiphenyl);2,2'-dihydroxybipphenol;2,2zzhlxy-Biphenol;ORTHOORTHOBIPHENOL;2,2''-BIPHENOL 99% | CAS: | 1806-29-7 | MF: | C12H10O2 | MW: | 186.21 | EINECS: | 217-303-0 | Product Categories: | Aromatic Phenols;Halogenated Heterocycles ,Triazines ,Thiophenes;Reagent for High-Performance Polymer Research;Functional Materials;Developer;Color Former & Related Compounds;Biphenyls (for High-Performance Polymer Research) | Mol File: | 1806-29-7.mol |  |
| 2,2'-Biphenol Chemical Properties |
Hazard Codes | Xi,Xn | Risk Statements | 37/38-41-36-22 | Safety Statements | 26-39-36/37/39 | WGK Germany | 2 | RTECS | DV4200000 | F | 8-9-23 | Autoignition Temperature | 324 °C | TSCA | Yes | HS Code | 29029090 | Toxicity | oms-hmn:lym 5 mmol/L CNREA8 45,2471,85 |
| 2,2'-Biphenol Usage And Synthesis |
Chemical Properties | Beige to greyish-beige powder | Uses | 2,2'-Dihydroxybiphenyl, is an important raw material and intermediate used in organic Synthesis, pharmaceuticals, agrochemicals and dyestuff. | Production Methods | 2,2'-Dihydroxybiphenyl is obtained by alkaline fusion of biphenylene oxide at ca. 300 ℃ (sometimes catalyzed by fluorene or carbazole) or by debutylation of 3,3',5,5'-tetra-tert-butyl-2,2'-dihydroxybiphenyl, which itself is produced by the oxidative coupling of 2,4-di-tert-butylphenol. 2,2'-Dihydroxy-5,5'-dimethylbiphenyl can be synthesized accordingly. | Definition | ChEBI: A member of the class of hydroxybiphenyls carrying hydroxy groups at positions 2 and 2'. | Safety Profile | Poison by intraperitoneal andintravenous routes. Human mutation data reported. Whenheated to decomposition it emits acrid smoke andirritating fumes. | Purification Methods | Crystallise the biphenyl repeatedly from toluene, then sublime it at 60o/10-4mm. [Beilstein 6 IV 6645.] |
| 2,2'-Biphenol Preparation Products And Raw materials |
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