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1-amino-3-chloropropan-2-ol, also known as beta-amino-1,3-chloropropan-2-ol, is a primary amino alcohol and a derivative of propane with the molecular formula C3H8ClNO. It is a colorless liquid with a mild odor and is soluble in water. However, it is corrosive and can cause severe skin and eye irritation, necessitating careful handling.

3920-12-5

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3920-12-5 Usage

Uses

Used in Pharmaceutical Industry:
1-amino-3-chloropropan-2-ol is used as an intermediate in the synthesis of chiral drugs for its unique chemical properties, facilitating the production of essential medications.
Used in Agrichemical Industry:
1-amino-3-chloropropan-2-ol is used as an intermediate in the synthesis of synthetic pesticides, such as propachlor, contributing to the development of effective agricultural chemicals.
Used in Surfactant and Detergent Production:
1-amino-3-chloropropan-2-ol is used as a key component in the manufacturing of surfactants and detergents, enhancing their cleaning and emulsifying properties.

Check Digit Verification of cas no

The CAS Registry Mumber 3920-12-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,2 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3920-12:
(6*3)+(5*9)+(4*2)+(3*0)+(2*1)+(1*2)=75
75 % 10 = 5
So 3920-12-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H8ClNO/c4-1-3(6)2-5/h3,6H,1-2,5H2

3920-12-5Relevant academic research and scientific papers

Synthesis of amine functionalized cellulose nanocrystals: Optimization and characterization

Akhlaghi, Seyedeh Parinaz,Zaman, Masuduz,Mohammed, Nishil,Brinatti, César,Batmaz, Rasim,Berry, Richard,Loh, Watson,Tam, Kam Chiu

, p. 48 - 55 (2015)

A simple protocol was used to prepare amine functionalized cellulose nanocrystals (CNC-NH2). In the first step, epichlorohydrin (EPH) was reacted with ammonium hydroxide to produce 2-hydroxy-3-chloro propylamine (HCPA). In the next step, HCPA was grafted to CNC using the etherification reaction in an organic solution media. Various reaction parameters, such as time, temperature, and reactant molar ratio were performed to determine the optimal reaction conditions. The final product (CNC-NH2(T)) was dialyzed for a week. Further purification via centrifugation yielded the sediment (CNC-NH2(P)) and supernatant (POLY-NH2). The presence of amine groups on the surface of modified CNC was confirmed by FTIR and the amine content was determined by potentiometric titration and elemental analysis. A high amine content of 2.2 and 0.6 mmol amine/g was achieved for CNC-NH2(T) and CNC-NH2(P), respectively. Zeta potential measurements confirmed the charge reversal of amine CNC from positive to negative when the pH was increased from 3 to 10. The flocculation of amine functionalized CNC due to its interactions with a negatively charged surfactant namely, sodium dodecyl sulfate (SDS) was investigated at pH 4. It showed promising results for applications, such as in flocculation of fine dispersions in water treatment. This simple and versatile synthetic method to produce high amine content CNC can be used for further conjugation as required for various applications.

An efficient chemoselective production of amines from azides using AlCl3/NaBH4

Raja Ram,Purushothama Chary,Salahuddin,Iyengar

, p. 935 - 937 (2007/10/03)

A practical reagent system AlCl3/NaBH4 is used for the preparation of amines from azides under mild reaction condition, in excellent yields.

A novel, chemoselective and efficient production of amines from azides using ZrCl4/NaBH4

Purushothama Chary,Raja Ram,Salahuddin,Iyengar

, p. 3559 - 3563 (2007/10/03)

A practical and cheaper reagent system ZrCl4/NaBH4 is used for the production of amines from azides is described.

A novel and efficient production of amines from azides using LiCl/NaBH4

Raja Ram,Purushothama Chary,Iyengar

, p. 4495 - 4500 (2007/10/03)

A practical and efficient reagent system LiCl/NaBH4 is used for the production of amines from azides is described.

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