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ChemicalBook--->CAS DataBase List--->13325-10-5

13325-10-5

13325-10-5 Structure

13325-10-5 Structure
IdentificationMore
[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 PropertiesBack 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 DataBack 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
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Diethyl ether-->Tetrahydrofuran-->N,N-Dimethylformamide-->Potassium hydroxide-->Acetonitrile-->Acetyl chloride-->Hydrazine hydrate-->Zinc chloride-->Cobalt chloride-->Potassium phthalimide-->4-Chloro-1-butanol-->1H-Isoindole-1,3(2H)-dione, 2-[4-(acetyloxy)butyl]--->2-(4-Hydroxybutyl)-2H-isoindole-1,3-dione-->4-aminobut-2-yn-1-ol hydrochloride-->Isobutyl nitrite-->1,4-DIAMINOBUTANE-->4-Aminobutyric acid
[Preparation Products]

4-bromobutan-1-amine
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

4-Amino-1-butanol(13325-10-5).msds
Hazard InformationBack 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].
[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.
Spectrum DetailBack Directory
[Spectrum Detail]

4-Amino-1-butanol(13325-10-5)MS
4-Amino-1-butanol(13325-10-5)1HNMR
4-Amino-1-butanol(13325-10-5)13CNMR
4-Amino-1-butanol(13325-10-5)IR1
4-Amino-1-butanol(13325-10-5)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

4-Amino-1-butanol, 98%(13325-10-5)
[Alfa Aesar]

4-Amino-1-butanol, 98%(13325-10-5)
[Sigma Aldrich]

13325-10-5(sigmaaldrich)
[TCI AMERICA]

4-Amino-1-butanol,>98.0%(GC)(13325-10-5)
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