- (R)-(-)-2-Amino-1-propanol
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- $34.00 / 1kg
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2024-04-08
- CAS:35320-23-1
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
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| | (R)-(-)-2-Amino-1-propanol Basic information |
| | (R)-(-)-2-Amino-1-propanol Chemical Properties |
| Melting point | 8 °C | | Boiling point | 173-176 °C(lit.) | | alpha | -17 º (c=neat) | | density | 0.965 | | refractive index | n20/D 1.450(lit.) | | Fp | 183 °F | | storage temp. | Keep in dark place,Inert atmosphere,2-8°C | | solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | | pka | 12.88±0.10(Predicted) | | form | Oily Liquid | | color | Clear colorless to light yellow | | Specific Gravity | 0.965 | | optical activity | [α]19/D 18°, neat | | Water Solubility | SOLUBLE | | Sensitive | Hygroscopic | | BRN | 1718866 | | CAS DataBase Reference | 35320-23-1(CAS DataBase Reference) | | NIST Chemistry Reference | (R)-(-)-2-Amino-1-propanol(35320-23-1) |
| Hazard Codes | C,Xi | | Risk Statements | 34-36/37/38 | | Safety Statements | 26-36/37/39-45-36 | | RIDADR | UN 2735 8/PG 2 | | WGK Germany | 3 | | F | 10-23 | | Hazard Note | Corrosive/Hygroscopic | | HazardClass | 8 | | PackingGroup | III | | HS Code | 29221990 |
| | (R)-(-)-2-Amino-1-propanol Usage And Synthesis |
| Chemical Properties | Colorless to light yellow liqui | | Uses | (R)-(-)-2-Amino-1-propanol has been used as a derivatizing agent for gossypol during the analysis of gossypol enantiomers in cottonseed by high-performance liquid chromatography. | | Application | R)-(-)-2-Amino-1-propanol is used as a chiral intermediate for the synthesis of pharmaceutical products and agrochemicals. It acts as additives in health care products and animal feed. It is a amino alcohol
obtained by reduction of d-alanine. This compound could be converted into the corresponding nonracemic
adenine derivative (R)-9-(1-Methyl-2-hydroxyethyl)adenine through minor variations on the classic
Montgomery sequence[1].
 | | General Description | (R)-(-)-2-Amino-1-propanol is a chiral secondary amine. | | References | [1] Jeffery A, et al. Synthesis of Acyclic Nucleoside and Nucleotide Analogues from
Amino Acids: A Convenient Approach to a PMEA±PMPA Hybrid. Tetrahedron, 2000; 56: 5077-5083. |
| | (R)-(-)-2-Amino-1-propanol Preparation Products And Raw materials |
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