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Merck
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重要文件

80645

Sigma-Aldrich

哌啶 溶液

suitable for peptide synthesis, 20% in DMF

同義詞:

Azacyclohexane, Cyclopentimine, Hexahydropyridine, Pentamethyleneimine

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About This Item

經驗公式(希爾表示法):
C5H11N
CAS號碼:
分子量::
85.15
Beilstein:
1421082
MDL號碼:
分類程式碼代碼:
12352005
PubChem物質ID:
NACRES:
NA.31

形狀

liquid

品質等級

濃度

20% in DMF

雜質

≤0.1% water

折射率

n20/D 1.434

密度

0.930 g/mL at 20 °C

應用

peptide synthesis

SMILES 字串

C1CCNCC1

InChI

1S/C5H11N/c1-2-4-6-5-3-1/h6H,1-5H2

InChI 密鑰

NQRYJNQNLNOLGT-UHFFFAOYSA-N

應用


  • 基于氧杂环的靶向强效抗菌和抗肿瘤吡喃类似物:合成和计算研究: 该研究重点介绍了哌啶溶液在新型吡喃类似物合成中的应用,通过先进的化学合成和计算建模技术,展示了其在增强抗菌和抗肿瘤性能方面的用途(El-Wahab et al., 2024)。

  • 杂环胺诱导的蜜蜂喂食威慑和触角反应.: 该研究利用哌啶溶液,考察了杂环胺对蜜蜂的影响,为植物-昆虫相互作用的化学生态学和农业害虫防治的潜在策略提供了有价值的见解 (Larson et al., 2021).

  • 氢氧化钠/哌啶介质的脱硅和磷改性对甲醇-丙烯转化反应的HZSM-5催化剂催化活性的影响。: 该研究使用哌啶溶液来改变HZSM-5催化剂的表面性质,显著提高了其在甲醇-丙烯转化过程中的性能,突出了其在工业催化中的应用(Safaei et al., 2021)。

  • 以酸性H(2)TiF(6)简单处理ERB-P沸石来合成MWW型钛硅酸盐及其在以H(2)O(2)进行的1-己烯液相环氧化反应中的催化性能。: 该研究利用哌啶溶液来合成新型钛硅酸盐材料,探索了其在己烯催化环氧化中的有效性,显示了哌啶促进先进材料合成的潜力(Guo et al., 2020)。

其他說明

销售限制可能适用

訊號詞

Danger

危險分類

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Eye Dam. 1 - Flam. Liq. 3 - Repr. 1B - Skin Corr. 1B

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

82.4 °F - closed cup

閃點(°C)

28 °C - closed cup

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Carmine Pasquale Cerrato et al.
Journal of materials chemistry. B, 8(47), 10825-10836 (2020-11-12)
Cell-penetrating peptides are a promising therapeutic strategy for a wide variety of degenerative diseases, ageing, and cancer. Among the multitude of cell-penetrating peptides, PepFect14 has been preferentially used in our laboratory for oligonucleotide delivery into cells and in vivo mouse
Xuwang Chen et al.
Bioorganic & medicinal chemistry, 20(12), 3856-3864 (2012-05-18)
A novel series of piperidine-linked amino-triazine derivatives were designed, synthesized and evaluated for in vitro anti-HIV activity as non-nucleoside reverse transcriptase inhibitors on the basis of our previous work. Screening results indicated that most compounds showed excellent activity against wild-type
Total synthesis of (-)-kopsinine by an asymmetric one-pot [n+2+3] cyclization.
Shingo Harada et al.
Chemistry, an Asian journal, 7(10), 2196-2198 (2012-08-22)
P Ricardo Girling et al.
Organic & biomolecular chemistry, 9(9), 3105-3121 (2011-03-11)
A review into the aza-Diels-Alder reaction, mainly concentrating on literature examples that form piperidin-4-ones from the reaction of imines and electron rich dienes or enones, either through a Lewis acidic/Brønsted acid approach or through the use of an organocatalyst. This
Elisabeth T Hennessy et al.
Science (New York, N.Y.), 340(6132), 591-595 (2013-05-04)
The manipulation of traditionally unreactive functional groups is of paramount importance in modern chemical synthesis. We have developed an iron-dipyrrinato catalyst that leverages the reactivity of iron-borne metal-ligand multiple bonds to promote the direct amination of aliphatic C-H bonds. Exposure

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