Identification | More | [Name]
1-Chlorohexadecane | [CAS]
4860-03-1 | [Synonyms]
1-CHLOROHEXADECANE 1-CHLOROHEXADECYNE CETYL CHLORIDE HEXADECYL CHLORIDE N-HEXADECYL CHLORIDE 1-Chlorhexadecan 1-Chlorohexadceane 1-chloro-hexadecan 1-Hexadecylchlorid Hexadecane,1-chloro- Palmityl chloride 1-Chlorohexadecane,97% 1-Chlorohexadecane, ca. 97% 1-CHLOROHEXADECANE-D33 98% Cetyl chloride, Hexadecyl chloride 1-Cyclohexadecane Barchlor(R) 16S | [EINECS(EC#)]
225-461-7 | [Molecular Formula]
C16H33Cl | [MDL Number]
MFCD00000959 | [Molecular Weight]
260.89 | [MOL File]
4860-03-1.mol |
Chemical Properties | Back Directory | [Appearance]
Liquid | [Melting point ]
8-14 °C(lit.)
| [Boiling point ]
149 °C1 mm Hg(lit.)
| [density ]
0.865 g/mL at 25 °C(lit.)
| [vapor pressure ]
129 mm Hg ( 21 °C)
| [refractive index ]
n20/D 1.449(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
Store below +30°C. | [solubility ]
<0.02g/l | [form ]
clear liquid | [color ]
Colorless to Almost colorless | [Water Solubility ]
0.02 g/L (20 ºC, Dec.) | [FreezingPoint ]
17.9℃ | [Usage]
Barchlor(R) 16S is used as chemical intermediate. | [BRN ]
1748498 | [CAS DataBase Reference]
4860-03-1(CAS DataBase Reference) | [NIST Chemistry Reference]
Hexadecane, 1-chloro-(4860-03-1) | [EPA Substance Registry System]
4860-03-1(EPA Substance) |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . | [RIDADR ]
UN 3082 9/PG 3
| [WGK Germany ]
3
| [TSCA ]
Yes | [HS Code ]
29031980 |
Hazard Information | Back Directory | [Chemical Properties]
1-Chlorohexadecane is Liquid
| [Uses]
1-Chlorohexadecane is used as chemical intermediate.
| [Synthesis Reference(s)]
Chemistry Letters, 7, p. 923, 1978 Synthetic Communications, 6, p. 21, 1976 DOI: 10.1080/00397917608062128 | [General Description]
The electron impact mass spectra of 1-chlorohexadecane was studied by sampling with supersonic molecular beams. |
|
|