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L-Phenylalaninol, 98%, Thermo Scientific Chemicals
CAS: 3182-95-4 | C9H13NO | 151.21 g/mol
$182.55 - $613.85
Chemical Identifiers
| CAS | 3182-95-4 |
|---|---|
| Molecular Formula | C9H13NO |
| Molecular Weight (g/mol) | 151.21 |
| MDL Number | MFCD00004732 |
| InChI Key | STVVMTBJNDTZBF-VIFPVBQESA-N |
| Synonym | l-phenylalaninol, s-2-amino-3-phenyl-1-propanol, s---2-amino-3-phenyl-1-propanol, s-2-amino-3-phenylpropan-1-ol, h-phenylalaninol, h-phe-ol, 2s-2-amino-3-phenylpropan-1-ol, phenylalaninol, --l-phenylalaninol, l-phenyl alaninol |
| PubChem CID | 447213 |
| IUPAC Name | (2S)-2-amino-3-phenylpropan-1-ol |
| SMILES | N[C@H](CO)CC1=CC=CC=C1 |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAA1158606
|
Thermo Scientific Chemicals
A1158606 |
5 g |
Each for $182.55
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AAA1158614
|
Thermo Scientific Chemicals
A1158614 |
25 g |
Each for $613.85
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Description
L-Phenylalaninol acts as an antiulcer agent that reduces the secretion of gastric acid and prevents ulcer formation. It inhibits intestinal absorption of L-phenylalanine making it a prospective treatment for phenylketonuria. Further, it reacts with nitriles to form oxazolines, which finds application in palladium-catalyzed allylic substitution. In addition to this, it is also used in amidation for chiral resolution and nicotinamide adenine dinucleotide modeling.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsL-Phenylalaninol acts as an antiulcer agent that reduces the secretion of gastric acid and prevents ulcer formation. It inhibits intestinal absorption of L-phenylalanine making it a prospective treatment for phenylketonuria. Further, it reacts with nitriles to form oxazolines, which finds application in palladium-catalyzed allylic substitution. In addition to this, it is also used in amidation for chiral resolution and nicotinamide adenine dinucleotide modeling.
Solubility
Soluble in chloroform, ethyl acetate, ethanol and methanol.
Notes
Incompatible with acids, acid chlorides, acid anhydrides and oxidizing agents.
Chemical Identifiers
| 3182-95-4 | |
| 151.21 | |
| STVVMTBJNDTZBF-VIFPVBQESA-N | |
| 447213 | |
| N[C@H](CO)CC1=CC=CC=C1 |
| C9H13NO | |
| MFCD00004732 | |
| l-phenylalaninol, s-2-amino-3-phenyl-1-propanol, s---2-amino-3-phenyl-1-propanol, s-2-amino-3-phenylpropan-1-ol, h-phenylalaninol, h-phe-ol, 2s-2-amino-3-phenylpropan-1-ol, phenylalaninol, --l-phenylalaninol, l-phenyl alaninol | |
| (2S)-2-amino-3-phenylpropan-1-ol |
Specifications
| 3182-95-4 | |
| 5 g | |
| Air Sensitive | |
| MFCD00004732 | |
| 2208238 | |
| Soluble in chloroform,ethyl acetate,ethanol and methanol. | |
| N[C@H](CO)CC1=CC=CC=C1 | |
| 151.21 | |
| 151.21 | |
| L-Phenylalaninol |
| 89°C to 94°C | |
| −23° (c=5 in ethanol) | |
| C9H13NO | |
| UN3259 | |
| l-phenylalaninol, s-2-amino-3-phenyl-1-propanol, s---2-amino-3-phenyl-1-propanol, s-2-amino-3-phenylpropan-1-ol, h-phenylalaninol, h-phe-ol, 2s-2-amino-3-phenylpropan-1-ol, phenylalaninol, --l-phenylalaninol, l-phenyl alaninol | |
| STVVMTBJNDTZBF-VIFPVBQESA-N | |
| (2S)-2-amino-3-phenylpropan-1-ol | |
| 447213 | |
| 98% |
Safety and Handling
GHS H Statement
H314-H318
Causes severe skin burns and eye damage.
Causes serious eye damage.
P260-P264b-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P501c
H314
DOTInformation : Transport Hazard Class: 8; Packing Group: III; Proper Shipping Name: AMINES, SOLID, CORROSIVE, N.O.S.
EINECSNumber : 221-674-4
RTECSNumber : UA6900000
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only