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Merck

C121509

Sigma-Aldrich

胱胺 二盐酸盐

96%

别名:

2,2ˊ-二乙氨基二硫 二盐酸盐, 2,2ˊ-二硫代二乙胺 二盐酸盐, 脱羧胱氨酸 二盐酸盐

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About This Item

线性分子式:
NH2CH2CH2SSCH2CH2NH2 · 2HCl
CAS号:
分子量:
225.20
Beilstein:
3616850
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

96%

形狀

powder

mp

217-220 °C (dec.) (lit.)

SMILES 字串

Cl[H].Cl[H].NCCSSCCN

InChI

1S/C4H12N2S2.2ClH/c5-1-3-7-8-4-2-6;;/h1-6H2;2*1H

InChI 密鑰

YUFRRMZSSPQMOS-UHFFFAOYSA-N

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應用

盐酸胱胺可作为合成二硫键交联的寡脱氧核糖核苷酸 和psammaplin A 的结构单元。它还可通过引入巯基用于功能化PGMA(聚(甲基丙烯酸缩水甘油酯)微球),并进一步制备银纳米颗粒(AgNP)。
肝素拮抗剂和巯基修饰剂

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产品编号
说明
价格

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

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

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Industrial & Engineering Chemistry Research, 54(25), 6480-6488 (2015)
Qianjiao Yang et al.
Molecules (Basel, Switzerland), 15(12), 8784-8795 (2010-12-04)
Psammaplin F, an unsymmetrical disulfide bromotyrosine, was isolated from the sponge Pseudoceratina purpurea in 2003. We reported here the first total synthesis of psammaplin F in 12% overall yield by employing Cleland's reagent reduction as key step. The longest linear
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