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等级
pharmaceutical primary standard
API类
phenylalanine
制造商/商品名称
USP
mp
270-275 °C (dec.) (lit.)
应用
pharmaceutical (small molecule)
格式
neat
储存温度
2-8°C
SMILES字符串
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
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一般描述
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.
应用
L-Phenylalanine USP reference standard suitable for use in specified USP compendial quality tests and assays.
Also used to prepare internal standard, standard, Sample, and system suitability solution during the assay and impurity analysis by using liquid chromatography coupled with UV detector according to the given below monographs of United States Pharmacopeia (USP):
Also used to prepare internal standard, standard, Sample, and system suitability solution during the assay and impurity analysis by using liquid chromatography coupled with UV detector according to the given below monographs of United States Pharmacopeia (USP):
- Acetylcysteine Solution
- Acetylcysteine
- Phenylalanine
- Glutathione
分析说明
These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.
其他说明
Sales restrictions may apply.
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Phenylalanine
United States Pharmacopeia, 3509-3509 (2023)
Glutathione
United States Pharmacopeia, 41(3), 5054-5054 (2023)
Acetylcysteine Solution
United States Pharmacopeia, 49(2), 82-82 (2020)
Acetylcysteine
United States Pharmacopeia, 49(2), 82-82 (2020)
Molecular genetics and metabolism, 86 Suppl 1, S22-S26 (2005-09-17)
Phenylketonuria (PKU) is an autosomal recessive genetic disorder in which mutations in the phenylalanine-4-hydroxylase (PAH) gene result in an inactive enzyme (PAH, EC 1.14.16.1). The effect is an inability to metabolize phenylalanine (Phe), translating into elevated levels of Phe in
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