- 1,3-Adamantanediol
-
- $0.00 / 1KG
-
2026-01-30
- CAS:5001-18-3
- Min. Order: 1KG
- Purity: 98%min
- Supply Ability: 30tons/month
- 1,3-Adamantanediol
-
- $5.00/ KG
-
2026-01-30
- CAS:5001-18-3
- Min. Order: 1KG
- Purity: 99% hplc
- Supply Ability: 500TONS
- 1,3-Adamantanediol
-
- $10.00 / 1KG
-
2026-01-30
- CAS:5001-18-3
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 10 mt
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| | 1,3-Adamantanediol Basic information |
| Product Name: | 1,3-Adamantanediol | | Synonyms: | 1,3-ADAMANTANDIOL;1,3-DIHYDROXYADAMANTANE;ADAMANTANE-1,3-DIOL;AKOS BC-0470;TRICYCLO[3.3.1.13,7]DECANE-1,3-DIOL;1,3-ADAMANTANEDIOL 98+%;1,3-Adamantanediol ,98.50%;1,3-Adamantanediol ,98.5% | | CAS: | 5001-18-3 | | MF: | C10H16O2 | | MW: | 168.23 | | EINECS: | 218-362-5 | | Product Categories: | Organic Building Blocks;Oxygen Compounds;Polyols;Building Blocks;Chemical Synthesis;Adamantanes;Pharmaceutical Intermediates;Adamantane derivatives | | Mol File: | 5001-18-3.mol |  |
| | 1,3-Adamantanediol Chemical Properties |
| Melting point | ~260 °C | | Boiling point | 320.4±10.0 °C(Predicted) | | density | 1.368±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,Room Temperature | | solubility | Chloroform (Slightly), Methanol (Slightly) | | form | Solid | | pka | 14?+-.0.40(Predicted) | | color | White to Off-White | | BRN | 7013501 | | InChI | InChI=1S/C10H16O2/c11-9-2-7-1-8(4-9)5-10(12,3-7)6-9/h7-8,11-12H,1-6H2 | | InChIKey | MOLCWHCSXCKHAP-UHFFFAOYSA-N | | SMILES | C12(O)CC3CC(CC(O)(C3)C1)C2 | | CAS DataBase Reference | 5001-18-3(CAS DataBase Reference) |
| WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29061990 | | Storage Class | 11 - Combustible Solids |
| | 1,3-Adamantanediol Usage And Synthesis |
| Chemical Properties | white crystal | | Uses | 1,3-Adamantanediol is used in the synthesis of novel dimethacrylate as possible dental monomers for dental resin mixtures. | | Synthesis | The procedure of Example 1 was repeated with the following adjustments: the catalyst was replaced with a vanadium (18 μmol) loaded V/Mont catalyst on montmorillonite; the dosage of adamantane was adjusted to 3 mM; tert-butyl acetate was chosen as the solvent; and the reaction conditions were set to continue at 100 °C for 96 h. The V/Mont catalysts were prepared according to the method described in Japanese Patent Application Publication (kokai) No. 2004-2234. ) No. 2004-2234. The specific operation includes: adding aqueous vanadium(III) chloride solution to montmorillonite (trade name: Kunipia F, produced by Kunimine Industries Co., Ltd.), followed by ion exchange, filtration, washing, drying and roasting at 800°C in air, to finally produce the desired catalysts. | | References | [1] Journal of the American Chemical Society, 1989, vol. 111, # 17, p. 6749 - 6757
[2] Journal of the American Chemical Society, 2005, vol. 127, # 44, p. 15391 - 15393
[3] Tetrahedron Letters, 1999, vol. 40, # 11, p. 2165 - 2168
[4] Tetrahedron Letters, 1999, vol. 40, # 11, p. 2165 - 2168
[5] Patent: US2006/235245, 2006, A1. Location in patent: Page/Page column 6-7 |
| | 1,3-Adamantanediol Preparation Products And Raw materials |
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