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重要文件

8.52122

Sigma-Aldrich

Fmoc-Asp(OAll)-OH

≥98.0% (acidimetric), for peptide synthesis, Novabiochem®

同義詞:

Fmoc-Asp(OAll)-OH

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About This Item

經驗公式(希爾表示法):
C22H21NO6
CAS號碼:
分子量::
395.41
MDL號碼:
分類程式碼代碼:
12352209
NACRES:
NA.22

product name

Fmoc-Asp(OAll)-OH, Novabiochem®

品質等級

產品線

Novabiochem®

化驗

≥98% (TLC)
≥98.0% (HPLC)
≥98.0% (acidimetric)

形狀

powder

反應適用性

reaction type: Fmoc solid-phase peptide synthesis

製造商/商標名

Novabiochem®

mp

111-114 °C

應用

peptide synthesis

官能基

carboxylic acid

儲存溫度

2-30°C

InChI

1S/C22H21NO6/c1-2-11-28-20(24)12-19(21(25)26)23-22(27)29-13-18-16-9-5-3-7-14(16)15-8-4-6-10-17(15)18/h2-10,18-19H,1,11-13H2,(H,23,27)(H,25,26)/t19-/m0/s1

InChI 密鑰

FBNFRRNBFASDKS-IBGZPJMESA-N

一般說明

Orthogonally-protected building block for the synthesis of peptides modified at the Asp side chain by Fmoc SPPS. See entry for 852072 for more details.04-12-1303

Associated Protocols and Technical Articles
Cleavage and Deprotection Protocols for Fmoc SPPS
Guide to Selection of Orthogonally -Protected Building Blocks for Fmoc SPPS

聯結

Replaces: 04-12-1303

分析報告

Color (visual): white to slight yellow to beige
Appearance of substance (visual): powder
Identity (IR): passes test
Optical rotation α 25/D (c=1 in DMF): -30.0 - -25.0 °
Purity (TLC(157A)): ≥ 98 %
Assay (HPLC, area%): ≥ 98.0 % (a/a)
Solubility (1 mmole in 2 ml DMF): clearly soluble
Assay (acidimetric): ≥ 98.0 %
Water (K. F.): ≤ 1.0 %

To see the solvent systems used for TLC of Novabiochem® products please click here.

法律資訊

Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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文章

Novabiochem® product range has one of the largest collections of orthogonally and quasi-orthogonally protected tri-functional amino acids. These derivatives are useful tools for the synthesis of cyclic and branched peptides and peptides carrying side-chain modifications.

Novabiochem® product range has one of the largest collections of orthogonally and quasi-orthogonally protected tri-functional amino acids. These derivatives are useful tools for the synthesis of cyclic and branched peptides and peptides carrying side-chain modifications.

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