Cas no 71750-71-5 (Alcohols, C>14)
Alcohols, C>14 Chemical and Physical Properties
Names and Identifiers
-
- Alcohols, C>14
- Alcohols, C>
- 1tetradecanol
- Lorol C14
- EINECS 268-107-7
- BRN 1742652
- nTetradecyl alcohol
- n-Tetradecan-1-ol
- D77653
- EINECS 272-490-6
- Tox21_300538
- EN300-19955
- Tetradecyl alcohol
- MYRISTYL ALCOHOL [MI]
- UNII-V42034O9PU
- 75782-87-5
- STL453593
- CHEMBL24022
- AKOS009031495
- MYRISTYL ALCOHOL (MART.)
- NCGC00254322-01
- Myristyl alcohol [NF]
- Lanette K
- Epal 14
- Loxanol V
- Tox21_201842
- Tetradecanol (7CI)
- EINECS 204-000-3
- HY-W004294
- Alfol 14
- Philcohol 1400
- S4827SZE3L
- Kalcohl 4098
- NCGC00259391-01
- Myristyl Alcohol, Pharmaceutical Secondary Standard; Certified Reference Material
- MYRISTYL ALCOHOL [FCC]
- Myristyl alcohol
- Myristyl alcohol, United States Pharmacopeia (USP) Reference Standard
- Myristic alcohol
- 1-Tetradecanol, Vetec(TM) reagent grade, 97%
- 1-Hydroxytetradecane
- 4-01-00-01864 (Beilstein Handbook Reference)
- 68855-56-1
- AI3-00943
- Nacol 14-95
- NSC-8549
- Myristyl cetyl alcohol
- NCGC00164345-02
- 14 OH
- (USEPA/OPP Pesticide Code: 001510)
- 1-Tetradecyl alcohol
- CS-W004294
- D05097
- UNII-S4827SZE3L
- tetradecylalcohol
- Conol 1495
- Alcohol(C14)
- 63393-82-8
- F7FCB87C-0FA4-412A-BC8C-BE5C952BC1E0
- MYRISTYL ALCOHOL [INCI]
- MYRISTYL ALCOHOL [WHO-DD]
- NSC8549
- MYRISTYL ALCOHOL [II]
- Lanette 14
- EC 616-261-4
- NCGC00164345-03
- Kalcol 4098
- V42034O9PU
- EINECS 267-009-1
- HSDB 5168
- NCGC00164345-01
- Tetradecan-1-ol
- Tetradecanol
- 1-TETRADECANOL
- n-Tetradecanol-1
- Polyethylene monoalcohol
- EINECS 269-790-4
- Lorol C 14
- C14 alcohol
- LMFA05000041
- MYRISTYL ALCOHOL (II)
- NS00002926
- n-Tetradecyl alcohol
- kalcohl 40
- EPA Pesticide Chemical Code 001510
- CAS-112-72-1
- EINECS 275-983-4
- 1-Tetradecanol, 97%
- Adol 18
- 1Hydroxytetradecane
- n-Tetradecanol
- MYRISTYL ALCOHOL (USP-RS)
- MFCD00004757
- 112-72-1
- DA-59961
- 71750-71-5
- BP-30124
- Q161683
- SCHEMBL20286
- NSC 8549
- DTXCID406926
- DTXSID0042456
- T0084
- DTXSID9026926
- CHEBI:77417
- 68002-95-9
- Myristyl alcohol; n-Tetradecan-1-ol
- Myristyl alcohol (NF)
- EC 204-000-3
- SDA 15-060-00
- 1-Tetradecanol, purum, >=95.0% (GC)
- 1-Tetradecanol, Selectophore(TM), >=99.0%
- MYRISTYL ALCOHOL [HSDB]
- MYRISTYL ALCOHOL [MART.]
- Dytol R-52
- EINECS 267-019-6
- Dytol R52
- 67762-41-8
- WLN: Q14
- Tetradecanol-1
- C14-15 alcohol
- 27196-00-5
- nTetradecanol1
- J-002824
- nTetradecanol
- MYRISTYL ALCOHOL [USP-RS]
- tetradecan1-ol
-
- MDL: MFCD00241475
- Inchi: 1S/C14H30O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h15H,2-14H2,1H3
- InChI Key: HLZKNKRTKFSKGZ-UHFFFAOYSA-N
- SMILES: OCCCCCCCCCCCCCC
Computed Properties
- Exact Mass: 214.229665576g/mol
- Monoisotopic Mass: 214.229665576g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 15
- Rotatable Bond Count: 12
- Complexity: 102
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- XLogP3: 6.2
- Topological Polar Surface Area: 20.2
Experimental Properties
- Density: 0.985?g/mL?at 25?°C(lit.)
- Solubility: toluene, MEK and hexane: soluble
- LogP: log Kow = 6.03
Alcohols, C>14 Security Information
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:3
Alcohols, C>14 Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 444472-250G |
Alcohols, C>14 |
71750-71-5 | average M | 250G |
¥538.7 | 2022-02-24 | |
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 444480-250G |
Alcohols, C>14 |
71750-71-5 | average M | 250G |
¥562.08 | 2022-02-24 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | SA04630-250g |
Alcohols, C>14 |
71750-71-5 | - | 250g |
¥708.0 | 2024-07-18 |
Alcohols, C>14 Related Literature
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1. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
-
Yaling Zhang,Chunhui Dai,Shiwei Zhou,Bin Liu Chem. Commun., 2018,54, 10092-10095
-
Nan Fu,Naphaporn Chiewchan,Xiao Dong Chen Food Funct., 2020,11, 211-220
-
Eunju Nam,Jiyeon Han,Sunhee Choi,Mi Hee Lim Chem. Commun., 2021,57, 7637-7640
Additional information on Alcohols, C>14
Properties and Applications of Alcohols, C≥14 (CAS No. 71750-71-5)
Alcohols, C≥14, identified by the Chemical Abstracts Service Number (CAS No.) 71750-71-5, represent a class of linear or branched aliphatic alcohols with carbon chains ranging from 14 to higher carbon numbers. These compounds are widely utilized in various industrial and scientific applications due to their unique chemical properties and versatility. The increasing demand for specialized chemical intermediates in pharmaceuticals, agrochemicals, and material science has made Alcohols, C≥14 a subject of significant research interest.
The molecular structure of Alcohols, C≥14 consists of a hydroxyl (-OH) group attached to a saturated hydrocarbon chain. The general formula for these alcohols can be represented as CnH2n+1OH, where n ranges from 14 to higher values. The presence of the hydroxyl group imparts polar characteristics to these compounds, enabling strong hydrogen bonding and solubility in both polar and non-polar solvents. This property makes them valuable in formulating solvents, emulsifiers, and surfactants.
In recent years, Alcohols, C≥14 have garnered attention in the field of drug development and biochemistry. Their long hydrocarbon chains provide a lipophilic environment that can enhance the bioavailability of certain pharmaceutical compounds. Researchers have explored their potential as carriers for drug delivery systems, particularly in formulations requiring controlled release. For instance, studies have demonstrated the efficacy of Alcohols, C≥14 in enhancing the stability and absorption of poorly soluble drugs by forming micelles or liposomes.
Moreover, the chemical reactivity of Alcohols, C≥14 allows for further functionalization through various reactions such as esterification, etherification, and oxidation. These derivatives find applications in synthesizing complex molecules used in fragrances, polymers, and specialty chemicals. The ability to modify their structure makes them indispensable in organic synthesis and industrial chemistry.
The agrochemical industry also benefits from the use of Alcohols, C≥14 as intermediates in the production of pesticides and herbicides. Their role in enhancing the formulation stability and bioavailability of active ingredients has been well-documented. Additionally, their environmental compatibility has been a focus area, with research efforts aimed at developing biodegradable versions that minimize ecological impact.
Recent advancements in material science have highlighted the use of Alcohols, C≥14 in developing advanced materials such as lubricants and coatings. Their high viscosity and thermal stability make them suitable for high-performance applications where conventional solvents fail. Researchers are exploring their potential in creating self-healing materials and smart coatings that can adapt to environmental changes.
The analytical chemistry domain has also seen significant contributions from Alcohols, C≥14. Their unique spectroscopic properties allow for precise identification and quantification using techniques such as nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry (MS). This has enabled scientists to study complex mixtures and understand reaction mechanisms more effectively.
In conclusion, Alcohols, C≥14 (CAS No. 71750-71-5) are multifunctional compounds with a wide range of applications across multiple industries. Their chemical properties make them invaluable in pharmaceuticals, agrochemicals, material science, and analytical chemistry. As research continues to uncover new uses for these compounds, their importance is expected to grow further.
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