1-PENTADECENE
1-PENTADECENE Basic information
- Product Name:
- 1-PENTADECENE
- Synonyms:
-
- 1-PENTADECENE 98%
- 1-Pentadecene 
- 1-PENTADECENE, 98%1-PENTADECENE, 98%1-PENTADECENE, 98%1-PENTADECENE, 98%
- 1-PENTADECENE
- Pentadec-1-ene
- Pentadecene
- Pentadecene,1-
- 1-Pentadecene,98%
- CAS:
- 13360-61-7
- MF:
- C15H30
- MW:
- 210.4
- EINECS:
- 236-414-5
- Product Categories:
-
- 1-Olefins (GC Standard)
- Analytical Chemistry
- Standard Materials for GC
- Acyclic
- Alkenes
- Organic Building Blocks
- Alpha Sort
- Chemical Class
- Hydrocarbons
- NeatsGasoline, Diesel,&Petroleum
- OlefinsVolatiles/ Semivolatiles
- P
- PA - PEN
- P-SAlphabetic
- Substance classes
- Mol File:
- 13360-61-7.mol
1-PENTADECENE Chemical Properties
- Melting point:
- −4 °C(lit.)
- Boiling point:
- 268-269 °C(lit.)
- Density
- 0.775 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.439(lit.)
- Flash point:
- >230 °F
- storage temp.
- Sealed in dry,Room Temperature
- form
- clear liquid
- color
- Colorless
- Specific Gravity
- 0.775
- Water Solubility
- Not miscible or difficult to mix in water.
- BRN
- 1751011
- InChI
- 1S/C15H30/c1-3-5-7-9-11-13-15-14-12-10-8-6-4-2/h3H,1,4-15H2,2H3
- InChIKey
- PJLHTVIBELQURV-UHFFFAOYSA-N
- SMILES
- CCCCCCCCCCCCCC=C
- CAS DataBase Reference
- 13360-61-7(CAS DataBase Reference)
- EPA Substance Registry System
- 1-Pentadecene (13360-61-7)
Safety Information
- Safety Statements
- 23-24/25
- WGK Germany
- 3
- TSCA
- TSCA listed
- HS Code
- 2901.29.1050
- Storage Class
- 10 - Combustible liquids
MSDS
- Language:English Provider:SigmaAldrich
1-PENTADECENE Usage And Synthesis
Chemical Properties
CLEAR COLORLESS TO LIGHT YELLOW LIQUID
Uses
1-Pentadecene serves as a growth medium for the strain CV2803T. It is a common semiochemical of flour beetles.
Definition
ChEBI: An unbranched fifteen-carbon alkene with one double bond between C-1 and C-2.
Synthesis
To a 10 mL Schlenk reaction tube (F891410 reaction tube, 10 mL capacity, mill 14/20) was added the photocatalyst palladium chloride (2 mol%, 0.7 mg), 4,5-bis(diphenylphosphino)-9,9-dimethyloxanthene (L1) (3 mol%, 3.5 mg), 2-(dicyclohexylphosphino)biphenyl (L2) (4 mol%. 2.8 mg) and active aliphatic NHPI ester (0.2 mmol, 80.2 mg). The air in the tube was completely displaced with argon three times, and then 2,4,6-trimethylpyridine (0.2 mmol, 24.2 mg), 2 mL of N,N-dimethylacetamide (DMA) were added under argon atmosphere. The reaction system was stirred continuously for 15 h at room temperature under the irradiation of a 36 W blue LED lamp (using an IKA magnetic stirrer, RCT basic model, with a stirring speed of 500 rpm). After the reaction was completed, the reaction was quenched with H2O and the reaction solution was extracted with ethyl acetate (3*10 mL), and then the combined organic phases were concentrated by rotary evaporation (BUCHI rotary evaporator R-3). The concentrated residue was chromatographically separated by a column (C383040C with sand plate storage ball chromatography column, 35/20, effective length: 500 mm) to obtain the product.
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