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Outros documentos

P17008

Sigma-Aldrich

L-Phenylalanine

99%

Sinônimo(s):

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

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About This Item

Fórmula linear:
C6H5CH2CH(NH2)CO2H
Número CAS:
63-91-2
Peso molecular:
165.19
Beilstein:
1910408
Número CE:
200-568-1
Número MDL:
MFCD00064227
Código UNSPSC:
12352209
eCl@ss:
32160406
ID de substância PubChem:
329820104
NACRES:
NA.26

Ensaio

99%

forma

powder

atividade óptica

[α]25/D −32.7°, c = 2 in H2O

pureza óptica

ee: 98% (GLC)

cor

white

pf

270-275 °C (dec.) (lit.)

cadeia de caracteres SMILES

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

chave InChI

COLNVLDHVKWLRT-QMMMGPOBSA-N

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substituído por

Nº do produto
Descrição
Preços

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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DL-Phenylalanine ReagentPlus®, 99%

Sigma-Aldrich

147966

DL-Phenylalanine

Phenethylamine purified by redistillation, ≥99.5%

Sigma-Aldrich

407267

Phenethylamine

Millipore

Millipore

1.07256

L-Phenylalanine

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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