Identification | More | [Name]
5-Amino-1-pentanol | [CAS]
2508-29-4 | [Synonyms]
5-AMINO-1-PENTANOL 5-AMINO-N-AMYL ALCOHOL 5-AMINOPENTAN-1-OL 5-AMINOPENTANOL 5-HYDROXY-N-AMYLAMINE 5-HYDROXYPENTYLAMINE 5-PENTANOLAMINE H-APE(5)-OL NH2-(CH2)5-OH NH2-PEN-OH 1-Pentanol, 5-amino- 5-Aminopentanol-1 Aminopentanol 5-Amino-1-pentanol, 50% in water 5-Amino-1-pentanol, 50 wt.% aqueous solution 5-amino-1-pentanol solution 5-Aminopentan-1-ol, 50% aqueous solution 5-AMINO-1-PENTANOL 97% 5-Aminopentane-1-ol Pentanolamine | [EINECS(EC#)]
219-718-2 | [Molecular Formula]
C5H13NO | [MDL Number]
MFCD00008237 | [Molecular Weight]
103.16 | [MOL File]
2508-29-4.mol |
Chemical Properties | Back Directory | [Appearance]
clear colorless to brown liquid after melting | [Melting point ]
33-35 °C (lit.) | [Boiling point ]
120-122 °C/16 mmHg (lit.) | [density ]
0.99 g/mL at 20 °C
| [refractive index ]
n20/D 1.4615(lit.)
| [Fp ]
150 °F
| [storage temp. ]
2-8°C
| [solubility ]
Chloroform, Ethyl Acetate | [form ]
Oil | [pka]
15.16±0.10(Predicted) | [color ]
Yellow | [PH]
13.2 (500g/l, H2O, 20℃) | [Water Solubility ]
miscible | [Sensitive ]
Air Sensitive | [BRN ]
1732302 | [InChIKey]
LQGKDMHENBFVRC-UHFFFAOYSA-N | [CAS DataBase Reference]
2508-29-4(CAS DataBase Reference) | [NIST Chemistry Reference]
Pentanol, 5-amino-(2508-29-4) |
Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R22:Harmful if swallowed. R34:Causes burns. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
UN 3259 8/PG 3
| [WGK Germany ]
2
| [F ]
10-34 | [Hazard Note ]
Irritant | [HazardClass ]
8 | [PackingGroup ]
III | [HS Code ]
29221980 |
Hazard Information | Back Directory | [Description]
5-Amino-1-pentanol is a linker containing a hydroxyl group and amine group. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The amine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. | [Chemical Properties]
clear colorless to brown liquid after melting | [Uses]
5-Amino-1-pentanol has been used in the synthesis of S-glycosyl amino-acid building blocks. It has been used as starting reagent in the synthesis of aminofunctionalized 4-chloro-2,2′:6′,2′′-terpyridine. | [Uses]
5-Amino-1-pentanol is an aliphatic amino alcohol with potential plasma lipid-lowering properties. 5-Amino-1-pentanol and other amino alcohols are used as emulsifying agents in dry-cleaning soaps, wax
removers, cosmetics, paints and insecticides. | [General Description]
5-Amino-1-pentanol undergoes facile intramolecular cyclocondensation with piperidine and methyl or ethyl piperidine in the presence of methanol or ethanol over zeolite catalyst. |
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