| Identification | More | [Name]
4-Amino-1-butanol | [CAS]
13325-10-5 | [Synonyms]
4-AMINO-1-BUTANOL
4-AMINOBUTANOL
4-AMINOBUTYL ALCOHOL
4-AMINO-N-BUTYL ALCOHOL
4-HYDROXYBUTYLAMINE
4-HYDROXY-N-BUTYLAMINE
BUTANOLAMINE
DELTA-AMINO-N-BUTYL ALCOHOL
H-ABUT(4)-OL
N-ABU(4)-OL
NH2-(CH2)4-OH
1-Butanol, 4-amino-
4-aminobutan-1-ol
4-Aminobutanol-1
4-hdyroxybutylamine
4-hydroxybutanamine
H2NCH2(CH2)2CH2OH
4-Amino-1-Butanol98%
4-Aminobutane-1-ol | [EINECS(EC#)]
236-364-4 | [Molecular Formula]
C4H11NO | [MDL Number]
MFCD00008230 | [Molecular Weight]
89.14 | [MOL File]
13325-10-5.mol |
| Chemical Properties | Back Directory | [Appearance]
Very light clear yellow liquid | [Melting point ]
16-18 °C (lit.) | [Boiling point ]
206 °C (lit.) | [density ]
0.967 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D ~1.462(lit.)
| [Fp ]
226 °F
| [storage temp. ]
Store at R.T. | [solubility ]
Acetonitrile (Slightly), Chloroform (Sparingly), Methanol (Slightly) | [form ]
Liquid | [pka]
15.10±0.10(Predicted) | [color ]
Clear colorless to slightly yellow | [Water Solubility ]
MISCIBLE | [Sensitive ]
Air Sensitive & Hygroscopic | [BRN ]
1731411 | [Stability:]
Unstable in Aqueous Solution | [CAS DataBase Reference]
13325-10-5(CAS DataBase Reference) | [NIST Chemistry Reference]
NH2(CH2)4OH(13325-10-5) | [EPA Substance Registry System]
1-Butanol, 4-amino- (13325-10-5) |
| Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R34:Causes burns.
R22:Harmful if swallowed. | [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) .
S25:Avoid contact with eyes . | [RIDADR ]
UN 2735 8/PG 3
| [WGK Germany ]
3
| [F ]
34 | [HazardClass ]
8 | [PackingGroup ]
III | [HS Code ]
29221980 |
| Hazard Information | Back Directory | [Description]
4-Amino-1-butanol (4AB,13325-10-5) is an important pharmaceutical intermediate compound and a precursor of biodegradable polymers for gene delivery. It can be used in organic synthesis and biological properties studies, among others. In addition, 4-Amino-1-butanol (4AB) has been shown to have a higher CO2 solubility than 2-amino-1-ethanol (MEA), which is potentially useful in solving problems related to flue gas purification[1-2].
| [Chemical Properties]
Very light clear yellow liquid | [Uses]
4-Amino-1-butanol(13325-10-5) is a useful intermediate in a variety of organic synthesis. It is mainly used in personal-care products, preparation of water soluble cationic flocculants and ion exchange resins as well as in the preparation of beta-lactam antibiotics. It is used for the production of efficient anionic emulsifiers, nonionic polyethylene emulsions, water treatment, metal treatment and absorption of carbon dioxide gas. It is used as a pigment dispersion aid and curing agent in selected textile -resins.
| [Preparation]
4-Amino-1-butanol (4AB,13325-10-5) can be prepared by microbiological methods. we report for the first time the fermentative production of 4AB from glucose by metabolically engineered Corynebacterium glutamicum harboring a newly designed pathway comprising a putrescine (PUT) aminotransferase (encoded by ygjG) and an aldehyde dehydrogenase (encoded by yqhD) from Escherichia coli, which convert PUT to 4AB. Application of several metabolic engineering strategies such as fine-tuning the expression levels of ygjG and yqhD, eliminating competing pathways, and optimizing culture condition further improved 4AB production. Fed-batch culture of the final metabolically engineered C. glutamicum strain produced 24.7?g/L of 4AB[1].
| [Synthesis]
The general procedure for synthesizing 4-amino-1-butanol from the compound (CAS:412274-79-4) was as follows: intermediate D (5.15 g, 50 mmol) from Example 2 was added to a 100 mL three-necked flask containing 50 mL of anhydrous tetrahydrofuran. Lithium aluminum hydride (2.28 g, 60 mmol) was accurately weighed and added to the flask in slow batches, followed by turning on magnetic stirring. The reaction system was heated to reflux and maintained for 1 hour. Upon completion of the reaction, ethyl acetate was carefully added to quench the excess lithium aluminum hydride. Subsequently, 10% sodium hydroxide solution was slowly added dropwise until the drop was stopped when light yellow solid precipitation was observed. Solid impurities were removed by diafiltration and the organic phase was separated to obtain the organic phase. The organic phase was purified by rotary evaporation to remove the solvent and then purified by distillation under reduced pressure to give the final yellow oily liquid product 4-amino-1-butanol (3.3 g, calculated yield). | [References]
[1] CINDY PRICILIA SURYA PRABOWO. Microbial production of 4-amino-1-butanol, a four-carbon amino alcohol[J]. Biotechnology and Bioengineering, 2020. DOI:10.1002/bit.27438.
[2] ZULKIFLI IDRIS . Equilibrium solubility of carbon dioxide in aqueous solutions of 3-amino-1-propanol, 4-amino-1-butanol and 5-amino-1-pentanol at low partial pressures[J]. Fluid Phase Equilibria, 2015. DOI:10.1016/j.fluid.2014.11.028.
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