| Identification | More | [Name]
Batyl alcohol | [CAS]
544-62-7 | [Synonyms]
1-O-OCTADECYL-RAC-GLYCEROL
2 3-DIHYDROXYPROPYL-1-OCTADECYL ETHER
3-N-OCTADECYL-1,2-PROPANEDIOL
3-N-OCTADECYLOXY-1,2-PROPANEDIOL
3-OCTADECYLOXY-1,2-PROPANEDIOL
3-OCTADECYLOXYPROPANE-1,2-DIOL
BATILOL
(+)-BATYL ALCOHOL
BATYL ALCOHOL
DL-3-OCTADECYLOXY-1,2-PROPANEDIOL
DL-BATYL ALCOHOL
GLYCEROL-1-OCTADECYL ETHER
GLYCEROL ALPHA-MONOSTEARYL ETHER
ICCB 70985
1,2-Propanediol,3-(octadecyloxy)-
1-o-octadecylglycerol
2,3-Dihydroxy-1-oc-tadecyloxypropane
2-Propanediol,3-(octadecyloxy)-1
3-(octadecyloxy)-2-propanediol
alpha-octadecyletherofglycerol | [EINECS(EC#)]
208-874-7 | [Molecular Formula]
C4H10O | [MDL Number]
MFCD00004720 | [Molecular Weight]
74.12 | [MOL File]
544-62-7.mol |
| Chemical Properties | Back Directory | [Melting point ]
71-73 °C (lit.) | [alpha ]
D20 +1.14° (c = 6.6 in CHCl3) | [Boiling point ]
419.64°C (rough estimate) | [density ]
0.9975 (rough estimate) | [refractive index ]
1.5192 (estimate) | [storage temp. ]
-15°C | [solubility ]
Chloroform (Slightly), Methanol (Slightly, Heated) | [form ]
Solid | [pka]
13.68±0.20(Predicted) | [color ]
White to Off-White | [Merck ]
1011 | [BRN ]
1725677 | [CAS DataBase Reference]
544-62-7(CAS DataBase Reference) | [EPA Substance Registry System]
544-62-7(EPA Substance) |
| Safety Data | Back Directory | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
TZ0960000
| [HS Code ]
29094990 |
| Hazard Information | Back Directory | [Uses]
Batyl Alcohol is used to synthesize amphiphilic alkylglycerolipids with antitumor activities. It is also used in cosmetic compounds for prevention or treatment of erythema or dermatitis or promotion of wound healing. | [Definition]
ChEBI: An alkylglycerol that is glycerol in which one of the primary hydroxy groups has been converted to the corresponding octadecyl ether. It is used in cosmetics as a stabilising ingredient and skin-conditioning agent. | [Purification Methods]
Batyl alcohol crystallises from aqueous Me2CO, EtOH or pet ether (b 40-60o). [Taguchi & Armarego Med Res Rev 18 pp43-88 1998, Beilstein 1 IV 2758.] |
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