C12-14 醇（CAS 80206-82-2）：分子式 C13H28O、分子量 200.36。
| CAS号 | 80206-82-2 |
|---|---|
| 分子式 | C13H28O |
| 分子量 | 200.36 |
| 熔点 | 32.5 °C |
| 沸点 | 525 °F at 760 mmHg (USCG, 1999) |
| LogP | 5.7 |
| 应用领域 | Uses: Used as a lubricant、antifoam agent、and chemical intermediate for detergents and other products、[HSDB]、Used as intermediate for plasticizers and other compounds、CHEM INT FOR DITRIDECYL PHTHALATE PLASTICIZER、FOR ISODECYL TRIDECYL PHTHALATE PLASTICIZER、FOR DITRIDECYL MALEATE、FOR ETHOXYLATED TRIDECYL ALCOHOL、FOR ALKOXYLATED TRIDECYL ALCOHOL、FOR TRIDECYL PHOSPHITE、FOR TRIDECYL GLYCERYL ESTER SULFONATE、FOR TRIDECYL SULFATE SODIUM SALT、FOR TRIDECYL THIOGLYCOLATE、FOR DITRIDECYL SULFOSUCCINATE、SODIUM SALT、FOR TRIDECYL 3-MERCAPTOPROPIONATE、Esters for synthetic lubricants、detergents、in other tridecyl compounds、perfumery、commercial mixt of isomers、Chemical intermediate for detergents-eg、its ethoxylate (as mixture)、Use Classification: Fragrance Ingredients、Cosmetics -> Refatting、Viscosity controlling、Emollient、Emulsion stabilizing、Industry Uses: Surfactant (surface active agent)、Consumer Uses: Surfactant (surface active agent)、Methods of Manufacturing: OXO REACTION OF CARBON MONOXIDE AND HYDROGEN WITH PROPYLENE TETRAMER、FOLLOWED BY HYDROGENATION OF THE RESULTING ALDEHYDE、Oxo process from C15 hydrocarbons.、Reaction of C11-C14 linear internal olefins with synth gas over a modified cobalt catalyst (modified oxo process) produces a mixt of n- & iso- alcohols (n-isomer predominates)、reaction of olefins with synth gas followed by hydrogenation makes branched & linear primary alcohols.、Tridecyl alcohol is produced from tetrapropylene by the oxo process for use only as a processing aid in polyvinyl chloride resins.、Formulations、Preparations: Grade: Technical、Consumption Patterns: OVER 90% AS A CHEM INT FOR PHTHALATE PLASTICIZERS AND APPROX 8% AS A CHEM INT FOR ETHOXYLATED TRIDECYL ALCOHOL (1972)、U.S. Production: 2023: 75、000、000 - <150、000 lb、2022: 25、000 - <75、2021: <75、2020: <75、(1972) 8.8X10+9 GRAMS、(1974) 9.2X10+9 GRAMS、(1990) >1 million-10 million pounds、(1994) >10 thousand-500 thousand pounds、(1998) >10 million-50 million pounds、(2002) >10 million-50 million pounds、(1982) 3.4X10+10 G (EST、IN C12-C15 ALCOHOLS)、U.S. Imports: (1972) No Data、(1975) No Data、U.S. Exports: (1972) No Data、General Manufacturing Information: Petrochemical Manufacturing、1-Tridecanol: ACTIVE、Tridecyl alcohol is、a commercial mixture of isomers. |
登记用途：Uses: Used as a lubricant、antifoam agent、and chemical intermediate for detergents and other products、[HSDB]、Used as intermediate for plasticizers and other compounds、CHEM INT FOR DITRIDECYL PHTHALATE PLASTICIZER、FOR ISODECYL TRIDECYL PHTHALATE PLASTICIZER、FOR DITRIDECYL MALEATE、FOR ETHOXYLATED TRIDECYL ALCOHOL、FOR ALKOXYLATED TRIDECYL ALCOHOL、FOR TRIDECYL PHOSPHITE、FOR TRIDECYL GLYCERYL ESTER SULFONATE、FOR TRIDECYL SULFATE SODIUM SALT、FOR TRIDECYL THIOGLYCOLATE、FOR DITRIDECYL SULFOSUCCINATE、SODIUM SALT、FOR TRIDECYL 3-MERCAPTOPROPIONATE、Esters for synthetic lubricants、detergents、in other tridecyl compounds、perfumery、commercial mixt of isomers、Chemical intermediate for detergents-eg、its ethoxylate (as mixture)、Use Classification: Fragrance Ingredients、Cosmetics -> Refatting、Viscosity controlling、Emollient、Emulsion stabilizing、Industry Uses: Surfactant (surface active agent)、Consumer Uses: Surfactant (surface active agent)、Methods of Manufacturing: OXO REACTION OF CARBON MONOXIDE AND HYDROGEN WITH PROPYLENE TETRAMER、FOLLOWED BY HYDROGENATION OF THE RESULTING ALDEHYDE、Oxo process from C15 hydrocarbons.、Reaction of C11-C14 linear internal olefins with synth gas over a modified cobalt catalyst (modified oxo process) produces a mixt of n- & iso- alcohols (n-isomer predominates)、reaction of olefins with synth gas followed by hydrogenation makes branched & linear primary alcohols.、Tridecyl alcohol is produced from tetrapropylene by the oxo process for use only as a processing aid in polyvinyl chloride resins.、Formulations、Preparations: Grade: Technical、Consumption Patterns: OVER 90% AS A CHEM INT FOR PHTHALATE PLASTICIZERS AND APPROX 8% AS A CHEM INT FOR ETHOXYLATED TRIDECYL ALCOHOL (1972)、U.S. Production: 2023: 75、000、000 - <150、000 lb、2022: 25、000 - <75、2021: <75、2020: <75、(1972) 8.8X10+9 GRAMS、(1974) 9.2X10+9 GRAMS、(1990) >1 million-10 million pounds、(1994) >10 thousand-500 thousand pounds、(1998) >10 million-50 million pounds、(2002) >10 million-50 million pounds、(1982) 3.4X10+10 G (EST、IN C12-C15 ALCOHOLS)、U.S. Imports: (1972) No Data、(1975) No Data、U.S. Exports: (1972) No Data、General Manufacturing Information: Petrochemical Manufacturing、1-Tridecanol: ACTIVE、Tridecyl alcohol is、a commercial mixture of isomers.。
C12-14 醇 是一种化工化合物，登记 CAS 号为 80206-82-2，分子式 C13H28O（分子量 200.36）。
登记 CAS 号：80206-82-2
其分子式 C13H28O 由 13 个碳、28 个氢、1 个氧 组成。
别名/同义词：C12-14 醇 · Alcohols, C12-14
C12-14 醇 的 CAS 登记号为 80206-82-2。
分子式 C13H28O，分子量 200.36。
别名/同义词：C12-14 醇、Alcohols, C12-14。
登记用途：Uses: Used as a lubricant、antifoam agent、and chemical intermediate for detergents and other products、[HSDB]、Used as intermediate for plasticizers and other compounds、CHEM INT FOR DITRIDECYL PHTHALATE PLASTICIZER、FOR ISODECYL TRIDECYL PHTHALATE PLASTICIZER、FOR DITRIDECYL MALEATE、FOR ETHOXYLATED TRIDECYL ALCOHOL、FOR ALKOXYLATED TRIDECYL ALCOHOL、FOR TRIDECYL PHOSPHITE、FOR TRIDECYL GLYCERYL ESTER SULFONATE、FOR TRIDECYL SULFATE SODIUM SALT、FOR TRIDECYL THIOGLYCOLATE、FOR DITRIDECYL SULFOSUCCINATE、SODIUM SALT、FOR TRIDECYL 3-MERCAPTOPROPIONATE、Esters for synthetic lubricants、detergents、in other tridecyl compounds、perfumery、commercial mixt of isomers、Chemical intermediate for detergents-eg、its ethoxylate (as mixture)、Use Classification: Fragrance Ingredients、Cosmetics -> Refatting、Viscosity controlling、Emollient、Emulsion stabilizing、Industry Uses: Surfactant (surface active agent)、Consumer Uses: Surfactant (surface active agent)、Methods of Manufacturing: OXO REACTION OF CARBON MONOXIDE AND HYDROGEN WITH PROPYLENE TETRAMER、FOLLOWED BY HYDROGENATION OF THE RESULTING ALDEHYDE、Oxo process from C15 hydrocarbons.、Reaction of C11-C14 linear internal olefins with synth gas over a modified cobalt catalyst (modified oxo process) produces a mixt of n- & iso- alcohols (n-isomer predominates)、reaction of olefins with synth gas followed by hydrogenation makes branched & linear primary alcohols.、Tridecyl alcohol is produced from tetrapropylene by the oxo process for use only as a processing aid in polyvinyl chloride resins.、Formulations、Preparations: Grade: Technical、Consumption Patterns: OVER 90% AS A CHEM INT FOR PHTHALATE PLASTICIZERS AND APPROX 8% AS A CHEM INT FOR ETHOXYLATED TRIDECYL ALCOHOL (1972)、U.S. Production: 2023: 75、000、000 - <150、000 lb、2022: 25、000 - <75、2021: <75、2020: <75、(1972) 8.8X10+9 GRAMS、(1974) 9.2X10+9 GRAMS、(1990) >1 million-10 million pounds、(1994) >10 thousand-500 thousand pounds、(1998) >10 million-50 million pounds、(2002) >10 million-50 million pounds、(1982) 3.4X10+10 G (EST、IN C12-C15 ALCOHOLS)、U.S. Imports: (1972) No Data、(1975) No Data、U.S. Exports: (1972) No Data、General Manufacturing Information: Petrochemical Manufacturing、1-Tridecanol: ACTIVE、Tridecyl alcohol is、a commercial mixture of isomers.。
C12-14 醇（CAS 80206-82-2）的独立参考数据，整理自公开化学数据库。
| CAS Registry Number | 80206-82-2 |
|---|---|
| PubChem CID | 8207 |
| Molecular formula | C13H28O |
| IUPAC name | tridecan-1-ol |
| UNII (FDA) | 8I9428H868 |
| Molecular Weight | 200.36 |
|---|---|
| XLogP3 | 5.7 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 11 |
| Exact Mass | 200.214015512 |
| Monoisotopic Mass | 200.214015512 |
| Topological Polar Surface Area | 20.2 |
| Heavy Atom Count | 14 |
| Boiling Point | 525 °F at 760 mmHg (USCG, 1999) |
|---|---|
| Boiling Point | 152 °C at 14 mm Hg |
| Boiling Point | 155.00 to 156.00 °C. @ 15.00 mm Hg |
| Boiling Point | 274 °C |
| Melting Point | 32.5 °C |
| Melting Point | 32.00 to 33.00 °C. @ 760.00 mm Hg |
| Melting Point | 30-32 °C |
| Flash Point | 250 °F (USCG, 1999) |
| Flash Point | 121 °C |
| Flash Point | 250 °F (121 °C) (Open cup) |
1-TRIDECANOL; Tridecan-1-ol; 112-70-9; Tridecyl alcohol; n-Tridecan-1-ol; n-Tridecyl alcohol; n-Tridecanol; DTXSID2021947; DTXCID901947; 8I9428H868; NSC-5252; 1-tridecyl alcohol; RefChem:907858; 203-998-8; Tridecanol; 26248-42-0
| Regulatory & Food Contact | FDA Cumulative Estimated Daily Intake (CEDI): FCS FDA Inventory of Food Contact Substances Listed in 21 CFR: FCS CIR / INCI: Emulsion stabilizing; Emollient; Viscosity controlling; Refatting |
|---|---|
| GHS notification summary | 3.1% (75 / 2412) |
| GHS notification summary | 3.1% (75 / 2412) |
|---|---|
| Reported hazard statements | H315 (13.3%), H318 (19.9%), H319 (12.7%), H400 (72.8%), H410 (64.5%), H412 (14.8%) |
This chemical does not meet GHS hazard criteria for 3.1% (75 of 2412) of reports.
H315 (13.3%): Causes skin irritation [Warning Skin corrosion/irritation]
Alcohols, C12-14 · CAS 80206-82-2 · C13H28O. UNII 8I9428H868. Boiling Point: 525 °F at 760 mmHg (USCG, 1999); Boiling Point: 152 °C at 14 mm Hg; Boiling Point: 155.00 to 156.00 °C. @ 15.00 mm Hg.
数据来源：PubChem / Wikidata；与随货 COA 不一致时以 COA 为准。
English page: Alcohols, C12-14