13325-10-5 Usage
Description
4-Amino-1-butanol is a very light clear yellow liquid that serves as a useful intermediate in a variety of organic synthesis processes.
Uses
Used in Personal Care Products:
4-Amino-1-butanol is used as a component in personal-care products for its ability to enhance the formulation and effectiveness of these products.
Used in Water Treatment:
4-Amino-1-butanol is used as a water-soluble cationic flocculant for water treatment processes, aiding in the purification and management of water quality.
Used in Ion Exchange Resins:
4-Amino-1-butanol is utilized in the preparation of ion exchange resins, which are essential in various industrial applications for the removal or recovery of specific ions.
Used in Pharmaceutical Industry:
4-Amino-1-butanol is used in the preparation of beta-lactam antibiotics, which are crucial in the development of life-saving medications.
Used in Chemical Industry:
4-Amino-1-butanol is used for the production of efficient anionic emulsifiers and nonionic polyethylene emulsions, which are vital in various chemical processes.
Used in Metal Treatment:
4-Amino-1-butanol is employed in metal treatment processes, where it aids in the management and improvement of metalworking fluids and processes.
Used in Carbon Capture:
4-Amino-1-butanol is used for the absorption of carbon dioxide gas, playing a role in environmental efforts to mitigate greenhouse gas emissions.
Used in Textile Industry:
4-Amino-1-butanol is used as a pigment dispersion aid and curing agent in selected textile-resins, enhancing the quality and performance of textile products.
Used in Research and Development:
4-Amino-1-butanol serves as a linker in the synthesis of highly branched poly(β-amino esters) (HPAEs) for gene delivery, contributing to advancements in genetic research and medicine.
Used in Polymer Science:
4-Amino-1-butanol is used as a side chain to modulate antimicrobial and hemolytic activities of copolymers, which is important in the development of new materials with specific properties.
Used in Organic Synthesis:
4-Amino-1-butanol is utilized in the total synthesis of complex organic compounds such as (+)-fawcettimine, (+)-fawcettidine, and (?)-lycojapodine A, showcasing its versatility in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 13325-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,2 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13325-10:
(7*1)+(6*3)+(5*3)+(4*2)+(3*5)+(2*1)+(1*0)=65
65 % 10 = 5
So 13325-10-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H11NO/c5-3-1-2-4-6/h6H,1-5H2/p+1
13325-10-5Relevant articles and documents
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Barlow
, p. 2225,2226, 2229 (1951)
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Catalytic hydrogenation of amino acids to amino alcohols with complete retention of configuration
Tamura, Masazumi,Tamura, Riku,Takeda, Yasuyuki,Nakagawa, Yoshinao,Tomishige, Keiichi
, p. 6656 - 6659 (2014)
Rh-MoOx/SiO2 is an effective heterogeneous catalyst for selective hydrogenation of amino acids to amino alcohols in a water solvent. MoOx modification of Rh drastically enhanced the activity and improved the selectivity and ee. Various amino alcohols were obtained in high yields (90-94%) with complete retention of configuration. This journal is the Partner Organisations 2014.
Preparation method of 4-aminobutanol
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Page/Page column 5-9, (2018/11/03)
The invention provides a preparation method of 4-aminobutanol. The method comprises the steps of taking potassium phthalimide and 4-chlorbutanol as raw materials, and preparing an intermediate in thepresence of a solvent and a phase transfer catalyst; and
METHOD FOR PRODUCING CIS- AND TRANS-ENRICHED MDACH
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, (2017/09/23)
A process for preparing trans-enriched MDACH, including: distilling an MDACH starting mixture in the presence of an auxiliary, which is an organic compound having a molar mass of 62 to 500 g/mol, a boiling point at least 5° C. above the boiling point of cis,cis-2,6-diamino-1-methylcyclohexane, and 2 to 4 functional groups, each of which is independently an alcohol group or a primary, secondary or tertiary amino group. The MDACH starting mixture includes 0 to 100% by weight of 2,4-MDACH and 0 to 100% by weight of 2,6-MDACH, based on the total amount of MDACH present in the MDACH starting mixture. The MDACH starting mixture includes both trans and cis isomers. Trans-enriched MDACH includes 0 to 100% by weight of 2,4-MDACH and 0 to 100% by weight of 2,6-MDACH, where the proportion of trans isomers in the mixture is higher than the proportion of trans isomers in the MDACH starting mixture.