Introduction:Basic information about CAS 673-06-3|D-phenylalanine, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | D-phenylalanine |
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| CAS Number | 673-06-3 | Molecular Weight | 165.189 |
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| Density | 1.2±0.1 g/cm3 | Boiling Point | 307.5±30.0 °C at 760 mmHg |
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| Molecular Formula | C9H11NO2 | Melting Point | 273-276 °C(lit.) |
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| MSDS | USA | Flash Point | 139.8±24.6 °C |
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Names
| Name | D-phenylalanine |
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| Synonym | More Synonyms |
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D-phenylalanine BiologicalActivity
| Description | D-Phenylalanine is the synthetic dextro isomer of phenylalanine. D-Phenylalanine inhibits biofilm development of Pseudoalteromonas sp. SC2014[1]. |
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| Related Catalog | Research Areas >>OthersSignaling Pathways >>Others >>Others |
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| References | [1]. Li E, et al. D-Phenylalanine inhibits biofilm development of a marine microbe, Pseudoalteromonas sp. SC2014. FEMS Microbiol Lett. 2016 Sep;363(18). |
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Chemical & Physical Properties
| Density | 1.2±0.1 g/cm3 |
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| Boiling Point | 307.5±30.0 °C at 760 mmHg |
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| Melting Point | 273-276 °C(lit.) |
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| Molecular Formula | C9H11NO2 |
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| Molecular Weight | 165.189 |
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| Flash Point | 139.8±24.6 °C |
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| Exact Mass | 165.078979 |
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| PSA | 63.32000 |
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| LogP | 1.11 |
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| Vapour Pressure | 0.0±0.7 mmHg at 25°C |
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| Index of Refraction | 1.576 |
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| InChIKey | COLNVLDHVKWLRT-MRVPVSSYSA-N |
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| SMILES | NC(Cc1ccccc1)C(=O)O |
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| Water Solubility | 27 g/L (20 ºC) |
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Toxicological Information
CHEMICAL IDENTIFICATION - RTECS NUMBER :
- AY7533000
- CHEMICAL NAME :
- Alanine, phenyl-, D-
- CAS REGISTRY NUMBER :
- 673-06-3
- LAST UPDATED :
- 199701
- DATA ITEMS CITED :
- 4
- MOLECULAR FORMULA :
- C9-H11-N-O2
- MOLECULAR WEIGHT :
- 165.21
- WISWESSER LINE NOTATION :
- QVYZ1R
HEALTH HAZARD DATAACUTE TOXICITY DATA - TYPE OF TEST :
- TDLo - Lowest published toxic dose
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Human
- DOSE/DURATION :
- 500 mg/kg/5W-I
- TOXIC EFFECTS :
- Gastrointestinal - hypermotility, diarrhea Gastrointestinal - nausea or vomiting
- REFERENCE :
- JACTDZ Journal of the American College of Toxicology. (Mary Ann Liebert, Inc., 1651 Third Ave., New York, NY 10128) V.1-12, 1982-1993. Discontinued. Volume(issue)/page/year: 1(3),124,1982
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intraperitoneal
- SPECIES OBSERVED :
- Rodent - rat
- DOSE/DURATION :
- 5452 mg/kg
- TOXIC EFFECTS :
- Behavioral - altered sleep time (including change in righting reflex) Lungs, Thorax, or Respiration - dyspnea Nutritional and Gross Metabolic - body temperature decrease
- REFERENCE :
- ABBIA4 Archives of Biochemistry and Biophysics. (Academic Press, Inc., 1 E. First St., Duluth, MN 55802) V.31- 1951- Volume(issue)/page/year: 64,319,1956 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - X5535 No. of Facilities: 7 (estimated) No. of Industries: 1 No. of Occupations: 2 No. of Employees: 307 (estimated) No. of Female Employees: 251 (estimated)
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Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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| Hazard Codes | Xi: Irritant; |
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| Risk Phrases | R34 |
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| Safety Phrases | S24/25 |
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| RIDADR | NONH for all modes of transport |
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| WGK Germany | 3 |
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| RTECS | AY7533000 |
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| HS Code | 29224995 |
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Customs
| HS Code | 2922499990 |
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| Summary | HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0% |
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Articles19
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| Synthesis, kinetic studies and pharmacological evaluation of mutual azo prodrugs of 5-aminosalicylic acid for colon-specific drug delivery in inflammatory bowel disease. Eur. J. Med. Chem. 44 , 3922-9, (2009) Colon-specific mutual azo prodrugs of 5-aminosalicylic acid with essential amino acids were synthesized for the management of inflammatory bowel disease. The structures were confirmed by elemental and... | |
| Carbonic anhydrase activators: activation of the human tumor-associated isozymes IX and XII with amino acids and amines. Bioorg. Med. Chem. 16 , 3530-6, (2008) The first activation study of the human carbonic anhydrase (hCA, EC 4.2.1.1) isoforms associated to tumors, hCA IX and XII, with a small library of natural and non-natural amino acids as well as aroma... | |
Synonyms
| (S)-phenylalanine |
| L-Phenylalanine |
| H-D-Phe-OH |
| (2S)-2-amino-3-phenylpropanoic acid |
| L-PHENYLALININE |
| α-Amino-β-phenylpropionic acid, L- |
| H-Phe-OH |
| Alanine, 3-phenyl- |
| L-phenylalanine zwitterion |
| S-phenylalanine |
| D-b-Phenylalanine |
| D-β-Phenylalanine |
| (S)-(-)-Phenylalanine |
| (R)-Phenylalanine |
| (S)-a-Amino-b-phenylpropionic Acid |
| Alanine, phenyl-, L- |
| L-2-Amino-3-phenylpropionic acid |
| (S)-2-Amino-3-phenylpropionic acid |
| (S)-2-Amino-3-phenylpropanoic acid |
| D-a-Amino-b-phenylpropionic Acid |
| C6H5CH2CH(NH2)COOH |
| (S)-a-Aminohydrocinnamic Acid |
| D-α-Amino-β-phenylpropionic acid |
| Phenylalanine |
| α-Aminohydrocinnamic acid, L- |
| (L)-Phenylalanine |
| Phenylalanine (VAN) |
| Phenylalanine, L- |
| phenylalanine D-form |
| Benzenepropanoic acid, α-amino-, (S)- |
| l-Phe |
| EINECS 211-603-5 |
| PhE |
| D-phenylalanine zwitterion |
| β-phenyl-L-alanine |
| d-Phe |
| (-)-Phenylalanine |
| (S)-α-Aminobenzenepropanoic acid |
| MFCD00004270 |
| (R)-(+)-Phenylalanine |
| α-Amino-β-phenylpropionic acid |
| (2R)-2-amino-3-phenylpropanoic acid |
| (S)-A-Aminobenzenepropanoic Acid |
| D-Phenylalanine |
| D-alpha-Amino-beta-phenylpropionic acid |