Video

Product No: AT8786

D-Phenylalanine, >98.0%(T)(HPLC)

Name: D-Phenylalanine
Brand: Chempure
Rating: 4 (1 reviews)

()

CAS Number

673-06-3

Total BLR Stock

Bulk Quote

Pack Size	Qty	Lead Time	Price	Quantity

About this item

IUPAC name	(2R)-2-amino-3-phenylpropanoic acid
canonical smiles	C1=CC=C(C=C1)CC(C(=O)O)N
inchi	InChI=1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m1/s1
inchi key	COLNVLDHVKWLRT-MRVPVSSYSA-N
molecular formula	C9H11NO2
synonyms	D-phenylalanine 673-06-3 H-D-Phe-OH (2R)-2-amino-3-phenylpropanoic acid Phenylalanine D-form
Compound Description	D-phenylalanine appears as needles or prisms. 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. D-Phenylalanine is a metabolite found in or produced by Escherichia coli . D-phenylalanine is a natural product found in Cyperus aromaticus, Daphnia pulex, and other organisms with data available. D-Phenylalanine is the synthetic dextro isomer of phenylalanine, an essential amino acid with anti-depressant and analgesic activities. D-Phenylalanine is converted into tyrosine and tyrosine in turn is converted into L-dopa, norepinephrine, and epinephrine, three key neurotransmitters. As a result this agent is associated with elevated levels of the neurotransmitters dopamine and norepinephrine in the brain, which may alleviate symptoms of depression. In addition, as an inhibitor of enkephalinase, which metabolizes endorphins, D-phenylalanine may be used to treat chronic pain through blocking the break down of endorphins .

Computed Properties

Molecular Weight:	165.19 g/mol
XLogP3:	-1.5
Hydrogen Bond Donor Count:	2
Hydrogen Bond Acceptor Count:	3
Rotatable Bond Count:	3
Exact Mass:	165.078978594 g/mol
Monoisotopic Mass:	165.078978594 g/mol
Topological Polar Surface Area:	63.3 Å²
Heavy Atom Count:	12
Formal Charge:	0
Complexity:	153
Isotope Atom Count:	0
Defined Atom Stereocenter Count:	1
Undefined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
Covalently-Bonded Unit Count:	1
Compound Is Canonicalized:	Yes

Related Compounds

Tyrosine

Phenylalanine

Histidine

Cinnamic Acid

Baclofen

Phenylpyruvic acid

3-Phenylpropionic acid

Metyrosine

2-Hydroxycinnamic acid, (2E)-

Racemetirosine

3'-Hydroxycinnamic acid

Fenclonine

Azaserine

D-Methionine

L-(-)-3-Phenyllactic acid

hazard signal	Warning
hazard classes and categories	Acute Tox. 4 (33.33%) Skin Irrit. 2 (66.67%) Eye Irrit. 2A (66.67%) STOT SE 3 (66.67%)
precautionary statement codes	P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
hazard statements	H302 (33.33%): Harmful if swallowed [Warning Acute toxicity, oral] H315 (66.67%): Causes skin irritation [Warning Skin corrosion/irritation] H319 (66.67%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] H335 (66.67%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

;

About this item

Documentation

Certificate of Analysis

Lot Number

Require a Sample Certificate of Analysis (COA) ?

CAS #

*This document is like a lab demo—an example Certificate of Analysis (COA) that showcases what a COA looks like but may not match the latest batch in all its glory. Think of it as a chemistry experiment: close, but not quite the final reaction!

Reviews

About this item

IUPAC name	(2R)-2-amino-3-phenylpropanoic acid
canonical smiles	C1=CC=C(C=C1)CC(C(=O)O)N
inchi	InChI=1S/C9H11NO2/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H,11,12)/t8-/m1/s1
inchi key	COLNVLDHVKWLRT-MRVPVSSYSA-N
molecular formula	C9H11NO2
synonyms	D-phenylalanine 673-06-3 H-D-Phe-OH (2R)-2-amino-3-phenylpropanoic acid Phenylalanine D-form
Compound Description	D-phenylalanine appears as needles or prisms. 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. D-Phenylalanine is a metabolite found in or produced by Escherichia coli . D-phenylalanine is a natural product found in Cyperus aromaticus, Daphnia pulex, and other organisms with data available. D-Phenylalanine is the synthetic dextro isomer of phenylalanine, an essential amino acid with anti-depressant and analgesic activities. D-Phenylalanine is converted into tyrosine and tyrosine in turn is converted into L-dopa, norepinephrine, and epinephrine, three key neurotransmitters. As a result this agent is associated with elevated levels of the neurotransmitters dopamine and norepinephrine in the brain, which may alleviate symptoms of depression. In addition, as an inhibitor of enkephalinase, which metabolizes endorphins, D-phenylalanine may be used to treat chronic pain through blocking the break down of endorphins .

Computed Properties

Molecular Weight:	165.19 g/mol
XLogP3:	-1.5
Hydrogen Bond Donor Count:	2
Hydrogen Bond Acceptor Count:	3
Rotatable Bond Count:	3
Exact Mass:	165.078978594 g/mol
Monoisotopic Mass:	165.078978594 g/mol
Topological Polar Surface Area:	63.3 Å²
Heavy Atom Count:	12
Formal Charge:	0
Complexity:	153
Isotope Atom Count:	0
Defined Atom Stereocenter Count:	1
Undefined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
Covalently-Bonded Unit Count:	1
Compound Is Canonicalized:	Yes

Related Compounds

Tyrosine

Phenylalanine

Histidine

Cinnamic Acid

Baclofen

Phenylpyruvic acid

3-Phenylpropionic acid

Metyrosine

2-Hydroxycinnamic acid, (2E)-

Racemetirosine

3'-Hydroxycinnamic acid

Fenclonine

Azaserine

D-Methionine

L-(-)-3-Phenyllactic acid

hazard signal	Warning
hazard classes and categories	Acute Tox. 4 (33.33%) Skin Irrit. 2 (66.67%) Eye Irrit. 2A (66.67%) STOT SE 3 (66.67%)
precautionary statement codes	P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
hazard statements	H302 (33.33%): Harmful if swallowed [Warning Acute toxicity, oral] H315 (66.67%): Causes skin irritation [Warning Skin corrosion/irritation] H319 (66.67%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] H335 (66.67%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Product No: AT8786

D-Phenylalanine, >98.0%(T)(HPLC)

Product No: AT8786

About this item

NAME AND IDENTIFIERS

CHEMICAL AND PHYSICAL PROPERTIES

Related Compounds

SAFETY AND HAZARDS

About this item

Documentation

Certificate of Analysis

Require a Sample Certificate of Analysis (COA) ?

Reviews

Product No: AT8786

About this item

NAME AND IDENTIFIERS

CHEMICAL AND PHYSICAL PROPERTIES

Related Compounds

SAFETY AND HAZARDS

Require a Sample Certificate of Analysis (COA) ?