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MilliporeSigma

W358509

L-Phenylalanine

99%, FCC

Synonym(s):

(S)-2-Amino-3-phenylpropionic acid

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$76.70

1 KG

$157.00

$76.70

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About This Item

Linear Formula:
C6H5CH2CH(NH2)CO2H
CAS Number:
63-91-2
Molecular Weight:
165.19
FEMA Number:
3585
Council of Europe no.:
10488
UNSPSC Code:
12164502
PubChem Substance ID:
24901797
Flavis number:
17.018
EC Number:
200-568-1
NACRES:
NA.21
MDL number:
MFCD00064227
Beilstein/REAXYS Number:
1910408
Organoleptic:
odorless
Grade:
Kosher
Biological source:
synthetic
Agency:
meets purity specifications of JECFA
Food allergen:
no known allergens

Key Documents

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SMILES string

N[C@@H](Cc1ccccc1)C(O)=O

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-/m0/s1

InChI key

COLNVLDHVKWLRT-QMMMGPOBSA-N

biological source

synthetic

grade

Kosher

agency

meets purity specifications of JECFA

reg. compliance

FCC, FDA 21 CFR 172.320

assay

99%

optical activity

[α]25/D -34.2°, c = 2 in H2O (dried basis)

mp

270-275 °C (dec.) (lit.)

solubility

H2O: soluble 16.5 g/L at 20 °C (completely)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

odorless

Quality Level

300, 400

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1 of 4

This Item
W358512405415202
L-Phenylalanine 99%, FCC

Sigma-Aldrich

W358509

L-Phenylalanine

L-Phenylalanine 99%, natural, FCC, FG

Sigma-Aldrich

W358512

L-Phenylalanine

L-Phenylalanine certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Supelco

40541

L-Phenylalanine

L-Phenylalanine

Millipore

5202

L-Phenylalanine

organoleptic

odorless

organoleptic

odorless

organoleptic

-

organoleptic

-

grade

Kosher

grade

FG, Halal, Kosher, natural

grade

certified reference material, TraceCERT®

grade

-

biological source

synthetic

biological source

corn

biological source

-

biological source

-

food allergen

no known allergens

food allergen

no known allergens

food allergen

-

food allergen

-

documentation

see Safety & Documentation for available documents

documentation

see Safety & Documentation for available documents

documentation

-

documentation

-

assay

99%

assay

99%

assay

-

assay

≥98.5% dry basis (titration)

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
SHBP7717
SHBP3983
SHBN5444
MKCH0860
MKBX9710V

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Ann Mullally et al.
Blood, 121(18), 3692-3702 (2013-03-15)
Interferon-α (IFNα) is an effective treatment of patients with myeloproliferative neoplasms (MPNs). In addition to inducing hematological responses in most MPN patients, IFNα reduces the JAK2V617F allelic burden and can render the JAK2V617F mutant clone undetectable in some patients. The
Vimesh A Avlani et al.
American journal of physiology. Endocrinology and metabolism, 304(10), E1097-E1104 (2013-03-28)
In addition to its acute effects on hormone secretion, epithelial transport, and shape change, the calcium-sensing receptor (CaSR) modulates the expression of genes that control cell survival, proliferation, and differentiation as well as the synthesis of peptide hormones and enzymes.
Stefanie Keil et al.
Pediatrics, 131(6), e1881-e1888 (2013-05-22)
Sapropterin dihydrochloride, the synthetic form of 6R-tetrahydrobiopterin (BH4), is an approved drug for the treatment of patients with BH4-responsive phenylketonuria (PKU). The purpose of this study was to assess genotypes and data on the long-term effects of BH4/sapropterin on metabolic
Minghua Tang et al.
The American journal of clinical nutrition, 99(4), 891-898 (2014-01-17)
Data on the protein requirements of elderly adults are limited, because it is impractical to conduct repeated nitrogen balance protocols in these vulnerable humans. This study was designed to determine the dietary protein requirement of elderly women by using the
John J Mitchell et al.
Genetics in medicine : official journal of the American College of Medical Genetics, 13(8), 697-707 (2011-05-11)
Phenylalanine hydroxylase deficiency is an autosomal recessive disorder that results in intolerance to the dietary intake of the essential amino acid phenylalanine. It occurs in approximately 1:15,000 individuals. Deficiency of this enzyme produces a spectrum of disorders including classic phenylketonuria
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