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Merck
CN

91331

L-苯基丙氨酸

analytical standard, for Nitrogen Determination According to Kjeldahl Method

别名:

(S)-2-氨基-4-苯基丙酸

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关于此项目

线性分子式:
C6H5CH2CH(NH2)CO2H
化学文摘社编号:
分子量:
165.19
EC Number:
200-568-1
UNSPSC Code:
85151701
PubChem Substance ID:
Beilstein/REAXYS Number:
1910408
MDL number:
NACRES:
NA.24
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InChI key

COLNVLDHVKWLRT-QMMMGPOBSA-N

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

SMILES string

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

grade

analytical standard

assay

≥99.0% (NT)

optical activity

[α]/D -34.0±0.5°, c = 2 in H2O

shelf life

limited shelf life, expiry date on the label

analyte chemical class(es)

amino acids, peptides, proteins

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

impurities

8.5%±0.2% total nitrogen acc. to Kjeldahl

loss

≤0.1% loss on drying

color

white

mp

270-275 °C (dec.) (lit.)

solubility

H2O: 0.1 M, clear, colorless

anion traces

chloride (Cl-): ≤50 mg/kg

cation traces

NH4+: ≤100 mg/kg

application(s)

food and beverages

format

neat

Quality Level

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存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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.
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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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

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