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35320-23-1

35320-23-1 Structure

35320-23-1 Structure
IdentificationMore
[Name]

(R)-(-)-2-Amino-1-propanol
[CAS]

35320-23-1
[Synonyms]

(+/-)-2-AMINO-1-PROPANOL
2-AMINO PROPANOL
(2R)-2-AMINO-1-PROPANOL
D-2-AMINO-PROPANOL
D-(-)-ALANINOL
D-ALANINOL
D-ALAOH
DL-2-AMINO-1-PROPANOL
DL-2-AMINO PROPANOL
DL-2-AMINOPROPYL-ALCOHOL
DL-ALANILOL
DL-ALANINOL
H-D-ALANINOL
H-D-ALA-OL
H-DL-ALA-OL
(R)-(-)-2-AMINO-1-PROPANOL
(R)-2-AMINO-1-PROPANOL
(R)-(-)-2-AMINOPROPANOL
(R)-1-Aminopropan-2-ol
D-amine propionic acid
[EINECS(EC#)]

228-207-3
[Molecular Formula]

C3H9NO
[MDL Number]

MFCD00008085
[Molecular Weight]

75.11
[MOL File]

35320-23-1.mol
Chemical PropertiesBack Directory
[Appearance]

Colorless to light yellow liqui
[Melting point ]

8 °C
[alpha ]

-17 º (c=neat)
[Boiling point ]

173-176 °C(lit.)
[density ]

0.965
[refractive index ]

n20/D 1.450(lit.)
[Fp ]

183 °F
[storage temp. ]

2-8°C
[solubility ]

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
[form ]

Oily Liquid
[pka]

12.88±0.10(Predicted)
[color ]

Clear colorless to light yellow
[Specific Gravity]

0.965
[Optical Rotation]

[α]19/D 18°, neat
[Water Solubility ]

SOLUBLE
[Sensitive ]

Hygroscopic
[Detection Methods]

GC
[BRN ]

1718866
[InChI]

1S/C3H9NO/c1-3(4)2-5/h3,5H,2,4H2,1H3/t3-/m1/s1
[InChIKey]

BKMMTJMQCTUHRP-GSVOUGTGSA-N
[SMILES]

C[C@@H](N)CO
[CAS DataBase Reference]

35320-23-1(CAS DataBase Reference)
[NIST Chemistry Reference]

(R)-(-)-2-Amino-1-propanol(35320-23-1)
[Storage Precautions]

Store under nitrogen;Air sensitive
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)
GHS05
[Signal word ]

Danger
[Hazard statements ]

H314
[Precautionary statements ]

P280-P303+P361+P353-P304+P340+P310-P305+P351+P338-P363-P405
[Hazard Codes ]

C,Xi
[Risk Statements ]

R34:Causes burns.
R36/37/38:Irritating to eyes, respiratory system and skin .
[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) .
S36:Wear suitable protective clothing .
[RIDADR ]

UN 2735 8/PG 2
[WGK Germany ]

3
[F ]

10-23
[Hazard Note ]

Corrosive/Hygroscopic
[HazardClass ]

8
[PackingGroup ]

III
[HS Code ]

29221990
[Storage Class]

8A - Combustible corrosive hazardous materials
[Hazard Classifications]

Eye Dam. 1
Skin Corr. 1B
Hazard InformationBack Directory
[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].
(R)-(-)-2-Amino-1-propanol
[General Description]

(R)-(-)-2-Amino-1-propanol is a chiral secondary amine.
[Synthesis]

D-Alanine

338-69-2

(R)-(-)-2-Amino-1-propanol

35320-23-1

General procedure for the synthesis of (R)-2-aminopropan-1-ol from D-alanine: The present embodiment relates to the synthesis of a class of intermediates of long-chain ethylpiperazine sulfonamide derivatives, in particular the preparation of (R)-2-aminopropan-1-ol. 150 mL of anhydrous THF and 1.1 g of LiAlH4 (29 mmol) were added to a dry three-necked flask and the reaction system was cooled to 0 °C. Subsequently, 4.9 g of D-alanine (55.0 mmol) was added to the reactor in batches, and the addition process lasted for 30 min. After the addition was completed, stirring was continued at 0 °C for 2 h. Then the temperature was gradually increased to reflux and the reflux reaction was maintained for 16 h. The reaction system was then cooled to 0 °C for 2 h. Upon completion of the reaction, the reaction system was cooled in an ice bath, and 100 mL of ether, 4.5 mL of water, 4.5 mL of 15% NaOH solution, and 12 mL of water were added slowly in sequence to quench the reaction. The reaction mixture was filtered through diatomaceous earth and the filtrate was collected. The filtrate was concentrated under reduced pressure to remove the solvent to give the crude product. The crude product was purified by silica gel column chromatography with the eluent of dichloromethane:ethanol=10:1 (v/v), resulting in 3.41 g of colorless oily product in 82.5% yield.

[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.
Spectrum DetailBack Directory
[Spectrum Detail]

(R)-(-)-2-Amino-1-propanol(35320-23-1)MS
(R)-(-)-2-Amino-1-propanol(35320-23-1)1HNMR
(R)-(-)-2-Amino-1-propanol(35320-23-1)13CNMR
(R)-(-)-2-Amino-1-propanol(35320-23-1)IR1
(R)-(-)-2-Amino-1-propanol(35320-23-1)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

(R)-(-)-2-Amino-1-propanol, 98%(35320-23-1)
[Alfa Aesar]

(R)-(-)-2-Amino-1-propanol, 98%(35320-23-1)
[Sigma Aldrich]

35320-23-1(sigmaaldrich)
[TCI AMERICA]

(R)-(-)-2-Amino-1-propanol,>98.0%(GC)(35320-23-1)
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