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Merck
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文件

91018

Supelco

(S)-NIFE

for chiral derivatization, ≥98.0%

同義詞:

N-(4-硝基苯氧基羰基)-L-苯基丙氨酸2-甲氧基乙酯

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About This Item

經驗公式(希爾表示法):
C19H20N2O7
CAS號碼:
分子量::
388.37
MDL號碼:
分類程式碼代碼:
12000000
PubChem物質ID:

等級

for chiral derivatization

化驗

≥98.0% (HPLC)
≥98.0%

形狀

powder

SMILES 字串

COCCOC(=O)[C@H](Cc1ccccc1)NC(=O)Oc2ccc(cc2)[N+]([O-])=O

InChI

1S/C19H20N2O7/c1-26-11-12-27-18(22)17(13-14-5-3-2-4-6-14)20-19(23)28-16-9-7-15(8-10-16)21(24)25/h2-10,17H,11-13H2,1H3,(H,20,23)/t17-/m0/s1

InChI 密鑰

ZSOUYIBYVUBOGT-KRWDZBQOSA-N

其他說明

HPLC 分析氨基酸的新型手性衍生化试剂;仲氨基酸类的衍生化

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Sonika Sethi et al.
Biomedical chromatography : BMC, 34(1), e4730-e4730 (2019-10-28)
LC separation of biologically and pharmaceutically important enantiomers (from racemic or non-racemic mixtures) remains a subject of importance. The present review article deals with the liquid chromatographic enantioseparation of chiral selective serotonin reuptake inhibitors (SSRIs), namely citalopram, paroxetine, sertraline and
E. Olajos et al.
Chromatographia, 54, 77-77 (2001)
Cecilia Barbas-Bernardos et al.
Journal of chromatography. A, 1611, 460598-460598 (2019-10-20)
In the nutrition field, there is a lack of understanding about the impact that dietary chiral composition may have on health, especially regarding cooked meals. Chiral amino acids (AAs) are naturally present in food and their proportion may vary quite
A. Peter et al.
Chromatographia, 52, 821-821 (2000)
Antal Péter et al.
Journal of chromatography. A, 948(1-2), 283-294 (2003-07-02)
A new chiral derivatizing agent, (S)-N-(4-nitrophenoxycarbonyl)phenylalanine methoxyethyl ester, (S)-NIFE, was applied for the high-performance liquid chromatographic separation of enantiomers of 19 unnatural secondary amino acids: proline, pipecolic acid analogues, piperazine-2-carboxylic acid, morpholine-3-carboxylic acid, thiomorpholine-3-carboxylic acid and analogues containing the 1,2,3,4-tetrahydroisoquinoline

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