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421669

Sigma-Aldrich

Asp-Phe

96%, for peptide synthesis

Sinónimos:

L-Aspartyl-L-phenylalanine, Aspartame acid

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About This Item

Fórmula lineal:
HOOCCH2CH(NH2)CONHCH(CH2C6H5)CO2H
Número de CAS:
13433-09-5
Peso molecular:
280.28
Beilstein/REAXYS Number:
2817528
EC Number:
236-557-3
MDL number:
MFCD00063155
UNSPSC Code:
12352209
PubChem Substance ID:
24866392
NACRES:
NA.22

product name

Asp-Phe, 96%

Quality Level

200

assay

96%

form

powder

optical activity

[α]20/D +12.5°, c = 1 in 0.5 M HCl

reaction suitability

reaction type: solution phase peptide synthesis

mp

236-239 °C (lit.)

application(s)

peptide synthesis

SMILES string

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

InChI

1S/C13H16N2O5/c14-9(7-11(16)17)12(18)15-10(13(19)20)6-8-4-2-1-3-5-8/h1-5,9-10H,6-7,14H2,(H,15,18)(H,16,17)(H,19,20)/t9-,10-/m0/s1

Inchi Key

YZQCXOFQZKCETR-UWVGGRQHSA-N

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Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
MKCX0043
0000305692
MKCT4953
MKCQ6241
MKCM8912

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L-Phenylalanine Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1100

L-Phenylalanine

Aspartame United States Pharmacopeia (USP) Reference Standard

USP

1043706

Aspartame

Patent blue VF sodium salt for microscopy

Sigma-Aldrich

76357

Patent blue VF sodium salt

Aspartame analytical standard

Supelco

47135

Aspartame

Methyl myristate analytical standard

Supelco

70129

Methyl myristate

Montserrat Andújar-Sánchez et al.
FEBS letters, 581(18), 3449-3454 (2007-07-10)
Somatic angiotensin I-converting enzyme (s-ACE) plays a central role in blood pressure regulation and has been the target of most antihypertensive drugs. A displacement isothermal titration calorimetry method has been used to accurately determine the binding constant of three strong
Y In et al.
Chemical & pharmaceutical bulletin, 48(3), 374-381 (2000-03-22)
As part of the series investigating the structural features of C-terminal amidated amino acids and peptides, three crystal structures of Z-Gly-Phe-NH2, Tyr-Lys-NH2, and Asp-Phe-NH2 were analyzed by the X-ray diffraction method, and their molecular conformations and intermolecular interactions were investigated.
W E Lipton et al.
Metabolism: clinical and experimental, 40(12), 1337-1345 (1991-12-01)
The dipeptide sweetener aspartame (N-L-alpha-aspartyl-L-phenylalanine, 1-methyl ester; alpha-APM) is relatively stable in dry powder form. However, when exposed to elevated temperature, extremes of pH and/or moisture, alpha-APM is converted into a variety of products. In aqueous solution alpha-APM decomposes to
D Grobelny et al.
Biochemical and biophysical research communications, 128(2), 960-964 (1985-04-30)
Aspartame (L-aspartyl-L-phenylalanine methyl ester, is a widely used artificIal sweetener. In humans and other animals aspartame is initially hydrolyzed to L-aspartyl-L-phenylalanine by intestinal esterases. L-Aspartyl-L-phenylalanine inhibits angiotensin converting enzyme purified from rabbit lungs with a Ki of 11 +/- 2
Kimber van Vliet et al.
Nutrients, 12(6) (2020-07-01)
Phenylketonuria and tyrosinemia type 1 are treated with dietary phenylalanine (Phe) restriction. Aspartame is a Phe-containing synthetic sweetener used in many products, including many 'regular' soft drinks. Its amount is (often) not declared; therefore, patients are advised not to consume
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