Identification | More | [Name]
6-Amino-1-hexanol | [CAS]
4048-33-3 | [Synonyms]
6-AMINO-1-HEXANOL 6-AMINOHEXANOL 6-AMINO-N-CAPROYL ALCOHOL H-ACP(6)-OL H-ACP-OL H-AHX-OL NH2-(CH2)6-OH RARECHEM AN KA 1117 TIMTEC-BB SBB006584 1-Amino-6-hexanol 1-Hexanol, 6-amino- 6-amino-hexano 6-Hydroxyhexylamine Amidohexylalkohol Aminohexyl alcohol aminohexylalcohol H2NCH2(CH2)4CH2OH Hexanol, 6-amino- 6-Aminohexan-1-ol 6-Hydroxy-1-hexylamine | [EINECS(EC#)]
223-748-1 | [Molecular Formula]
C6H15NO | [MDL Number]
MFCD00008241 | [Molecular Weight]
117.19 | [MOL File]
4048-33-3.mol |
Chemical Properties | Back Directory | [Appearance]
slightly yellow crystalline powder | [Melting point ]
54-58 °C (lit.) | [Boiling point ]
135-140 °C/30 mmHg (lit.) | [density ]
0.8872 (estimate) | [refractive index ]
1.4444 (estimate) | [Fp ]
133 °C
| [storage temp. ]
Store at?0-5°C | [solubility ]
DMSO (Slightly), Chloroform (Slightly), Methanol (Slightly) | [form ]
Crystals | [pka]
15.18±0.10(Predicted) | [color ]
Light yellow to brown | [Stability:]
Hygroscopic. Stable. Incompatible with strong oxidizing agents. | [Water Solubility ]
MISCIBLE | [Sensitive ]
Hygroscopic | [BRN ]
1732524 | [InChIKey]
SUTWPJHCRAITLU-UHFFFAOYSA-N | [CAS DataBase Reference]
4048-33-3(CAS DataBase Reference) | [NIST Chemistry Reference]
NH2(CH2)6OH(4048-33-3) | [EPA Substance Registry System]
4048-33-3(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 . S37/39:Wear suitable gloves and eye/face protection . S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [RTECS ]
MO8840000
| [F ]
3-10 | [HazardClass ]
IRRITANT, HYGROSCOPIC | [HS Code ]
29221990 |
Hazard Information | Back Directory | [Chemical Properties]
slightly yellow crystalline powder | [Uses]
6-Amino-1-hexanol is used in the synthesis of guanidino analogs of roscovitine, which is a cyclin-dependant kinase. Also used in the preparation of tocotrienols which maintain anticancer, antiprolifer
ative and antimigratory activity. Behery, F | [Synthesis]
By volume ratio, 1 part of 6-aminohexanoic acid was added to the reactor containing 15 parts of diethyl ether or dry toluene solution At 40 ℃ constant temperature, At 1500rpm / min speed, rapidly injected 2 parts of a solution of sodium borohydride. At 250W, ultrasonic treatment 20min. Then, dropwise under reflux, 8 parts of ethylene glycol solution. Dropwise addition time was 30 minutes. Finally, at 90 ℃ and at a rate of 800rpm/min, maintain temperature under stirring and react for 16 h to obtain the reaction crude product. (2) By the amount of parts count, step (1) preparation of 1 part of the reaction crude was added 6 parts water for hydrolysis. Undrego vacuum distillation, collecting 125 ℃ fraction, to obtain the 6-amino-1-hexanol product.
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