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D-Phenylalanine

D-Phenylalanine Structure
CAS No.
673-06-3
Chemical Name:
D-Phenylalanine
Synonyms
PHENYLALANINE;d-phe;H-D-PHE-OH;D-Phe-OH;(R)-PHENYLALANINE;(R)-2-amino-3-phenylpropanoic acid;NSC 25005;nci-c60195;Endorphenyl;D-Phenylalanin
CBNumber:
CB9773699
Molecular Formula:
C9H11NO2
Molecular Weight:
165.19
MOL File:
673-06-3.mol
MSDS File:
SDS
Modify Date:
2024/7/2 17:33:06

D-Phenylalanine Properties

Melting point 273-276 °C(lit.)
Boiling point 293.03°C (rough estimate)
alpha 33.5 º (c=2, H2O)
Density 1.1603 (rough estimate)
refractive index 34 ° (C=2, H2O)
storage temp. Store at RT.
solubility Methanol (Slightly), Water (Slightly)
form Powder
pka 2.2(at 25℃)
color White to off-white
Water Solubility 27 g/L (20 ºC)
Merck 14,7271
BRN 2804068
Stability Stable. Incompatible with strong oxidizing agents, acids, bases.
InChIKey COLNVLDHVKWLRT-MRVPVSSYSA-N
LogP 0.235 (est)
CAS DataBase Reference 673-06-3(CAS DataBase Reference)
EPA Substance Registry System D-Phenylalanine (673-06-3)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P271-P280
Hazard Codes  Xi,C
Risk Statements  34
Safety Statements  24/25-45-36/37/39-27-26
WGK Germany  3
RTECS  AY7533000
Hazard Note  Irritant
TSCA  Yes
HS Code  29224995
Toxicity TDLo orl-hmn: 500 mg/kg/5W-I:GIT JACTDZ 1(3),124,82
NFPA 704
0
1 0

D-Phenylalanine price More Price(12)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) P1751 D-Phenylalanine ≥98% (HPLC) 673-06-3 5G ₹1786.13 2022-06-14 Buy
Sigma-Aldrich(India) P1751 D-Phenylalanine ≥98% (HPLC) 673-06-3 25G ₹8454.33 2022-06-14 Buy
Sigma-Aldrich(India) P1751 D-Phenylalanine ≥98% (HPLC) 673-06-3 100G ₹24854.2 2022-06-14 Buy
TCI Chemicals (India) P0135 D-Phenylalanine 673-06-3 5G ₹2100 2022-05-26 Buy
TCI Chemicals (India) P0135 D-Phenylalanine 673-06-3 25G ₹5300 2022-05-26 Buy
Product number Packaging Price Buy
P1751 5G ₹1786.13 Buy
P1751 25G ₹8454.33 Buy
P1751 100G ₹24854.2 Buy
P0135 5G ₹2100 Buy
P0135 25G ₹5300 Buy

D-Phenylalanine Chemical Properties,Uses,Production

Description

D-Phenylalanine, also known as D-alpha-Amino-beta-phenylpropionic acid, is a kind of non-proteinogenic amino acid. The biological function of D-phenylalanine remains unclear. However, it has certain anti-depressant, analgesic activities and pharmacological activity at niacin receptor II. The mechanism action of its analgesic activity seems to originate from its inhibition of enkephalin degradation by the carboxypeptidase A. Enkephalins are part of your body’s natural pain relief system. When they are broken down by enkephalinase, this contributes to the sensation of pain. D-Phenylalanine is specifically thought to be beneficial for reducing feelings of chronic pain. D-phenylalanine has been used with mixed results to treat chronic pain, including pain caused by rheumatoid arthritis. The primary use of D-phenylalanine as a health supplement is the relief of discomfort.

Chemical Properties

White crystalline powder

Uses

D-Phenylalanine, the stereoisomer of L-Phenylalanine (P319415) has been used in the synthesis of Schaeffer’s acid analogues as important structures in tuberculostatic design. They exhibit the ability to inhibit Mycobacterium tuberculosis type II dehydroquinase.

Definition

ChEBI: D-phenylalanine is the D-enantiomer of phenylalanine. It is a phenylalanine and a D-alpha-amino acid. It is a conjugate base of a D-phenylalaninium. It is a conjugate acid of a D-phenylalaninate. It is an enantiomer of a L-phenylalanine. It is a tautomer of a D-phenylalanine zwitterion.

General Description

D-phenylalanine appears as needles or prisms.

Air & Water Reactions

Water soluble. Aqueous solutions are weakly acidic.

Reactivity Profile

D-alpha-Amino-beta-phenylpropionic acid may be light sensitive. D-alpha-Amino-beta-phenylpropionic acid reacts with strong oxidizing agents, acids and bases. . Act as weak acids in solution.

Fire Hazard

Flash point data for D-alpha-Amino-beta-phenylpropionic acid are not available, however D-alpha-Amino-beta-phenylpropionic acid is probably combustible.

Safety Profile

Mildly toxic by intraperitoneal route. Human systemic effects by ingestion: nausea, hypermotility, diarrhea. When heated to decomposition it emits toxic fumes of NOx.

References

https://www.alfa.com/en/catalog/A10572/
https://en.wikipedia.org/wiki/Phenylalanine
Christianson, D. W., et al. "Binding of D-phenylalanine and D-tyrosine to carboxypeptidase A. " Journal of Biological Chemistry264.22(1989):12849-53.

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D-PHENYLALANINE, >=98% (HPLC) D-beta-Phenyl-alpha-aminopropionic acid d-alpha-aminohydrocinnamic acid D-ALPHA-AMINO-BETA-PHENYL-PROPIONIC ACID D-2-AMINO-3-PHENYLPROPANOIC ACID D(+)-PHENYLALANINE D-PHENYLALANINE RARECHEM AB PP 0687 (R)-2-AMINO-3-PHENYLPROPIONIC ACID D-PHENYLALANINE, 99+% (98% EE/GLC) D-Phenylalanine,>99% D-α-Amino-β-phenylpropionic acid Alanine, phenyl-, D- (8CI) D-a-Amino-b-phenylpropionic acid D-b-Phenylalanine D-Phenylalanine (9CI) NSC 25005 D-Phenylalanin D-Phenglalanine,(R)-(+)-Phenglalanine H-D-PHE-OH D-PHENYLALANINE D-PHENYLALANINE ((R)-PHENYLALANINE) (2R)-2-Amino-3-phenylpropanoic acid (2R)-2-Amino-3-phenylpropionic acid (R)-2-Benzylglycine D-Phenylalanine≥ 99% (Assay) D-PHENYLALANINE extrapure CHR (R)-(+)-Phenylalanine, (R)-2-Amino-3-phenylpropionic acid, D-2-Amino-3-phenylpropanoic acid nci-c60195 D-Phenylalanine,(R)-2-Amino-3-phenylpropionic acid D-Phenylalanine Vetec(TM) reagent grade, >=98% NATEGLINIDE INTERMEDIATES D-Phenyl-d5-alanine-d3 Endorphenyl D-2-Amino-3-phenylpropionic acid D-3-Benzene-2-Amnopropanoic Acid D-α-Aminohydrocinnamic acid D-Phenylalanine, 99%, reagent grade D-Phenylalanine> D-Phenylalanine USP/EP/BP D-Phenylalanine,0.98 dextro-phenyl alanine D-phenylanaline D-Phe-OH d-phe H-D-PHE-OH (R)-PHENYLALANINE PHENYLALANINE (R)-2-amino-3-phenylpropanoic acid (R)-Phenylalanine (Intermediate) D-Phenylalanine (9CI, ACI) (2S)-2-amino-3-phenylpropanoic acid (phenylalanine) D-Phenylalanine(natural) 673-06-3 673-06-9 C6H5CH2CHNH2CO2H Specialty Synthesis Peptide Synthesis Amino Acid Derivatives