N,N-二异丙基乙胺

概述规格名称和识别符技术文档高级数据系统学分类三维结构质检证书（CoA,COO,BSE/TSE 和分析图谱) 化学和物理性质安全和危险性（GHS）此产品的引用文献技术文档和文章引用文献溶液计算器常见问题

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为什么选择此级别

精馏级提供 ≥99.5% 纯度，适用于对基线干扰要求严格的色谱和分析工作流程。

🌡

储存与运输

室温,充氩。DG运输。请查阅批次 COA 获取详细规格。

📋

质量文档

SDS、COA、产品数据表及规格说明书均可下载。可通过批号查询获取批次 COA。

📚

文献证明

在色谱分析、有机合成和交叉偶联反应领域已被 444 篇同行评审文献引用。

概述

溶于醇、醚等有机溶剂，呈碱性，易燃，易挥发，具有胺的气味，有刺激性。水中溶解度:3.9 g/L (20°C)。常用作质子清除剂，用于肽偶联、烯醇硼化、钯(0)催化的烯丙基磷酸酯和醋酸酯的烷氧基羰基化；也可在烯基砜合成中用作催化剂。

Usually used as Proton scavenger in peptide coupling,enolboration,Pd(0)-catalyzed alkoxycarbonylation of allyl phosphates and acetates;And also used as a catalyst in vinyl sulfone synthesis.

规格

别名

二异丙乙胺 | DIEA

英文别名

规格或纯度

精馏级, ≥99.5%

英文名称

N,N-Diisopropylethylamine

应用

常用作质子清除剂，用于肽偶联、烯醇硼化、钯(0)催化的烯丙基磷酸酯和醋酸酯的烷氧基羰基化；也可在烯基砜合成中用作催化剂。

储存条件

室温,充氩

运输条件

DG运输

纯度

≥99.5%

名称和识别符

PubChem SID

504755537

EC号

230-392-0

分子类型

小分子

IUPAC Name

N-ethyl-N-propan-2-ylpropan-2-amine

INCHI

1S/C8H19N/c1-6-9(7(2)3)8(4)5/h7-8H,6H2,1-5H3

InChi Key

JGFZNNIVVJXRND-UHFFFAOYSA-N

Smiles

CCN(C(C)C)C(C)C

Isomeric SMILES

CCN(C(C)C)C(C)C

UN Number

UN 3384

Packing Group

分子量

129.24

Beilstein号

4124745

Reaxy-Rn

605301

Reaxys-RN link address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605301&ln=

技术文档

📋 安全数据表 (SDS)

全面的危险、操作、储存及法规合规文件。

下载 SDS →

✅ 分析证书 (COA)

批次质量数据。输入批号以获取对应 COA。

查询 COA →

📊 产品数据表

产品规格和应用的快速参考摘要。

查看数据表 →

🔬 规格说明书

该级别的完整质量属性和验收标准。

查看规格说明 →

高级数据

系统学分类

分类树（Taxonomy Tree）

界（kingdom) 有机化合物
- 超类（Superclass) 有机氮化合物
  - 类（Class) 有机氮化合物
    - 亚类（Subclass）胺类
      - 第5级 (level 5) 叔胺
        第6级 (level 6) 三烷基胺

界（kingdom)	有机化合物
超类（Superclass)	有机氮化合物
类（Class)	有机氮化合物
亚类（Subclass）	胺类
中间层级节点（Intermediate Tree Nodes）	叔胺
直接上位类(Direct Parent)	三烷基胺
其他上位类（Alternative Parents）	有机光子化合物碳氢化合物衍生物
分子骨架（Molecular Framework)	脂肪族无环化合物
取代基（Substituents）	脂肪族非环化合物 - 烃衍生物 - 有机氮化合物 - 三元脂肪胺
描述（Description）	该化合物属于有机化合物中的三烷基胺类。这类化合物含有三烷基胺基团，其特征在于三个烷基基团精确地与氨基氮原子相连。
外部描述符（External Descriptors）	暂无

三维结构

交互式化学结构模型

球棍
棍棒
线框模型
空间填充
显示氢气
动画

化学和物理性质

密度

0.742

折光率

1.414

闪点(℉)

51.08 ℉

闪点(℃)

10.6°C

沸点

127°C

熔点

-45 °C

分子量

129.240 g/mol

XLogP3

2.200

氢键供体数Hydrogen Bond Donor Count

氢键受体数Hydrogen Bond Acceptor Count

可旋转键计数Rotatable Bond Count

精确质量Exact Mass

129.152 Da

单同位素质量Monoisotopic Mass

129.152 Da

拓扑极表面积Topological Polar Surface Area

3.200 Å²

重原子数Heavy Atom Count

形式电荷Formal Charge

复杂度Complexity

59.000

同位素原子数Isotope Atom Count

定义的原子立体中心计数Defined Atom Stereocenter Count

未定义的原子立体中心计数Undefined Atom Stereocenter Count

定义的键立体中心计数Defined Bond Stereocenter Count

未定义的键立体中心计数Undefined Bond Stereocenter Count

所有立体化学键的总数The total count of all stereochemical bonds

共价键合单元计数Covalently-Bonded Unit Count

安全和危险性（GHS）

一般危化品

象形图

GHS02, GHS05, GHS07, GHS08

信号词

危险

危险声明

H225: 高度易燃的液体和蒸气

H302: 吞食有害

H314: 造成严重的皮肤灼伤和眼睛损伤

H331: 吸入会中毒

H335: 可能引起呼吸道刺激

H402: 对水生生物有害

H411: 对水生生物有毒并具有长期持续影响

预防措施声明

P210: 远离热源，热表面，火花，明火和其他点火源。 - 禁止抽烟。

P233: 保持容器密闭。

P240: 地面/粘结容器和接收设备

P241: 使用防爆的[电气/通风/照明/.../]设备。

P242: 仅使用无火花的工具。

P243: 采取防静电措施

P261: 避免吸入灰尘/烟雾/气体/雾/蒸汽/喷雾

P264: 处理后要彻底洗手。

P330: 漱口

P303+P361+P353: 如皮肤（或头发）沾染：立即脱掉所有沾染的衣服。用水清洗皮肤/淋浴。

P304+P340: 如误吸入：将人转移到空气新鲜处，保持呼吸舒适体位。

P370+P378: 火灾时：使用干砂、干粉或抗醇泡沫灭火。

P405: 密闭存放

P501: 将内容物/容器处理到。。。

P264+P265: 处理后彻底洗手[和…]。不要触摸眼睛。

P301+P317: 如果被吞咽：请寻求医疗帮助。

P305+P354+P338: 如果进入眼睛：立即用水冲洗几分钟。取下隐形眼镜（如果有的话），并且操作简单。继续冲洗。

WGK Germany

Class

6.1 (3)

个人防护装备

Faceshields,full-face respirator (US),Gloves,Goggles,multi-purpose combination respirator cartridge (US),type ABEK (EN14387) respirator filter

质检证书（CoA,COO,BSE/TSE 和分析图谱)

C of A & Other Certificates(BSE/TSE, COO):

输入批号以搜索分析图谱:

通过匹配包装上的批号来查找并下载产品的 COA，每批产品都进行了严格的验证，您可放心使用！

找到106个结果

批号(Lot Number)	证书类型	货号
I2611312	分析证书	D109322
I2611568	分析证书	D109322
H2615325	分析证书	D109322
H2615326	分析证书	D109322
H2615499	分析证书	D109322
H2611191	分析证书	D109322
H2611192	分析证书	D109322
H2611359	分析证书	D109322
G2620347	分析证书	D109322
G2620350	分析证书	D109322
G2610456	分析证书	D109322
G2610457	分析证书	D109322
E2608374	分析证书	D109322
E2608375	分析证书	D109322
D2615272	分析证书	D109322
D2615273	分析证书	D109322
D2615424	分析证书	D109322
E2606203	分析证书	D109322
E2606204	分析证书	D109322
D2615270	分析证书	D109322
D2615271	分析证书	D109322
D2615425	分析证书	D109322
A2630509	分析证书	D109322
A2630510	分析证书	D109322
A2630620	分析证书	D109322
A2609198	分析证书	D109322
A2609199	分析证书	D109322
A2609436	分析证书	D109322
C2623024	分析证书	D109322
L2512463	分析证书	D109322
L2512464	分析证书	D109322
L2512524	分析证书	D109322
K2511334	分析证书	D109322
K2511339	分析证书	D109322
K2511517	分析证书	D109322
I2515247	分析证书	D109322
I2515248	分析证书	D109322
I2515701	分析证书	D109322
H2521331	分析证书	D109322
H2521332	分析证书	D109322
H2521394	分析证书	D109322
G2514222	分析证书	D109322
G2514223	分析证书	D109322
G2514402	分析证书	D109322
F2505401	分析证书	D109322
F2505404	分析证书	D109322
F2505424	分析证书	D109322
D2517369	分析证书	D109322
D2517425	分析证书	D109322
D2517452	分析证书	D109322
B2521297	分析证书	D109322
B2521300	分析证书	D109322
B2508049	分析证书	D109322
L2418558	分析证书	D109322
L2418559	分析证书	D109322
L2418584	分析证书	D109322
J2410301	分析证书	D109322
J2410302	分析证书	D109322
J2410303	分析证书	D109322
H2413213	分析证书	D109322
H2413214	分析证书	D109322
H2413453	分析证书	D109322
C2408347	分析证书	D109322
C2408370	分析证书	D109322
C2408414	分析证书	D109322
A2415141	分析证书	D109322
A2415253	分析证书	D109322
A2415254	分析证书	D109322
J2326278	分析证书	D109322
J2326279	分析证书	D109322
J2326280	分析证书	D109322
J2308451	分析证书	D109322
J2308452	分析证书	D109322
J2308453	分析证书	D109322
H2312055	分析证书	D109322
H2312122	分析证书	D109322
H2312129	分析证书	D109322
F2327068	分析证书	D109322
F2327069	分析证书	D109322
F2327070	分析证书	D109322
F2327074	分析证书	D109322
D23141448	分析证书	D109322
D23141468	分析证书	D109322
D23141474	分析证书	D109322
D23141480	分析证书	D109322
D23141508	分析证书	D109322
B2328823	分析证书	D109322
B2328824	分析证书	D109322
C2314351	分析证书	D109322
B2302345	分析证书	D109322
K2224323	分析证书	D109322
K2224326	分析证书	D109322
K2224341	分析证书	D109322
B2302346	分析证书	D109322
J2227238	分析证书	D109322
J2227239	分析证书	D109322
J2227316	分析证书	D109322
J2211787	分析证书	D109322
J2211850	分析证书	D109322
J2211880	分析证书	D109322
G2209106	分析证书	D109322
G2209109	分析证书	D109322
G2211003	分析证书	D109322
F2209135	分析证书	D109322
E2220207	分析证书	D109322
C2212500	分析证书	D109322

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Peptide synthesis Chiral amide

HATU 在困难偶联中的方法学价值：活性优势、手性保持与条件管理

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HATU

The Methodological Value of HATU in Difficult Couplings: Reactivity Advantages, Stereochemical Retention, and Condition Management

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HATU

Boc-Oxyma 的方法学价值：低消旋偶联、路线衔接与延伸用途

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多肽合成偶联试剂手性酰胺低消旋偶联试剂

The Methodological Value of Boc-Oxyma: Low-Racemization Coupling, Route Continuity, and Extended Applications

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Peptide synthesis coupling reagent Chiral amide Low racemic coupling reagent

多肽合成中的低消旋，不只是试剂选择：活化阶段的构型风险与实验控制思路

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多肽合成酰胺键构建消旋

Low Racemization in Peptide Synthesis Is Not Just About Reagent Choice: Stereochemical Risk During the Activation Stage and Practical Strategies for Experimental Control

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Peptide synthesis Amide bond construction Racemic

DSC 的方法学价值：NHS 型活化中间体的构建与选用判断

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DSC N,N′-二琥珀酰亚胺基碳酸酯

The Methodological Value of DSC: Building NHS-Type Activated Intermediates and Deciding When to Use Them

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DSC N,N′-disuccinimidyl carbonate

TCFH 的方法学价值：困难酰胺化中的应用优势与羧酸活化路径的切换逻辑

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羧酸缩合试剂 TCFH 强效缩合试剂

The Methodological Value of TCFH: Advantages in Challenging Amidation and the Switching Logic of Carboxylic Acid Activation Pathways

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carboxylic acid TCFH coupling reagents Strong condensing reagent

多肽合成中的低消旋控制：活化 α-氨基酸酯的逆向 N→C 成肽思路

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多肽合成低消旋

Low-Racemization Control in Peptide Synthesis: An Inverse N→C Peptide Synthesis Strategy via Activated α-Aminoesters

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Peptide synthesis Low-Racemization

炔酰胺缩合试剂：从低差向异构化活化路径到更接近实用的 N→C 反向成肽

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多肽合成酰胺键构建缩合试剂炔酰胺缩合试剂

Ynamide Coupling Reagents: From Low-Epimerization Activation Pathways to More Practically Usable N→C Inverse Peptide Synthesis

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Peptide synthesis Amide bond construction

多肽合成路线的判断逻辑：从 SPPS、LPPS 到重组表达的适用情形与判断依据

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多肽合成液相多肽合成多肽化学制备

Decision Logic for Peptide Synthesis Routes: Applicability and Criteria for Choosing among SPPS, LPPS, and Recombinant Expression

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Peptide synthesis Liquid-phase peptide synthesis

酰胺键形成中缩合剂选型的判断逻辑：活化路径、副反应、差向异构化、后处理与安全性

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缩合剂酰胺键形成酰胺键

Decision Logic for Selecting Coupling Reagents in Amide Bond Formation: Activation Pathways, Side Reactions, Epimerization, Workup, and Safety

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Amide bond formation condensing reagent Amide bond

羧酸预活化路线的实验选型逻辑：经典混合酸酐、CDI、磺酰氯与 Yamaguchi 体系的区别与适用情形

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手性酰胺键构建羧酸预活化

Experimental Selection Logic for Carboxylic Acid Preactivation Pathways: Differences and Suitable Use Cases for Classical Mixed Anhydrides, CDI, Sulfonyl Chloride Systems, and the Yamaguchi System

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chirality Amide bond formation Carboxylic acid preactivation

DBU 在不同体系中的反应角色：强有机碱、亲核催化与反应路径参与的实验判断

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DBU 双环脒类试剂

Reaction Roles of DBU in Different Systems: Experimental Judgment from a Strong Organic Base to Nucleophilic Catalysis and Participation in the Reaction Pathway

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DBU Bicyclic amidine reagents

Boc₂O 的选用不能只看保护引入：从底物亲核性、介质效应到脱保护路径的实验判断

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氨基甲酸酯 Boc₂O Boc 保护

Boc₂O Selection Cannot Be Judged by Protection Installation Alone: Experimental Decision-Making from Substrate Nucleophilicity and Medium Effects to Deprotection Pathways

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Boc₂O carbamate Boc protection

DMAP 不只是有机碱：从亲核酰基转移到酯化与大环内酯化的实验判断

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有机合成有机碱酯化酰基转移

DMAP Is More Than Just an Organic Base: Experimental Judgment from Nucleophilic Acyl Transfer to Esterification and Macrolactonization

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Organic synthesis Acyl transfer Organic base Esterification

HOPO 在碳二亚胺介导酰胺偶联中的实验判断：低消旋控制、适用场景与工艺考量

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偶联 HOPO 药物酰胺

Experimental Assessment of HOPO in Carbodiimide-Mediated Amide Coupling: Low-Racemization Control, Application Scenarios, and Process Considerations

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Conjugation HOPO Drug amide

五氟苯基体系的实验选用逻辑：从活性酯、预活化单体到下游转化的实验判断

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五氟苯酚 PFP-OH 氟苯基酯 PFP esters

Experimental Selection Logic for Pentafluorophenyl-Based Systems: Practical Judgment from Active Esters and Pre-Activated Monomers to Downstream Transformations

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Polypentafluorophenol PFP-OH PFP esters Pentafluorophenyl esters

SEM-Cl 的实验选用：从 O/N-SEM 保护、杂环定向官能化到受保护 C1 片段引入

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2-(三甲基硅烷基)乙氧甲基氯 SEM-Cl

Experimental Selection of SEM-Cl: From O/N-SEM Protection and Directed Functionalization of N-Heterocycles to the Introduction of Protected C1 Fragments

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SEM-Cl 2-(Trimethylsilyl)ethoxymethyl chloride

Oxyma 偶联体系的实验判断：偶联效率、消旋控制与 DIC 体系的 HCN 风险

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偶联 Oxyma 偶联体系 Oxyma 乙基 2-氰基-2-(羟亚胺基)乙酸酯

Experimental Judgment in Oxyma Coupling Systems: Coupling Efficiency, Racemization Control, and the HCN Risk in DIC-Based Systems

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Coupling Oxyma Oxyma Coupling Systems ethyl 2-cyano-2-(hydroxyimino)acetate OxymaPure

三光气在有机合成中的实验判断：按反应任务理解其选用逻辑

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有机合成三光气

Experimental Evaluation of Triphosgene in Organic Synthesis: Understanding Its Selection Logic Through Reaction Tasks

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Organic synthesis Triphosgene

4-[(叔丁基二甲基硅基)氧基]丁-1-醇：作为单保护 1,4-丁二醇构件和受保护 C4 连接臂的实验选型判断

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有机合成药物化学羟基保护基

4-[(tert-Butyldimethylsilyl)oxy]butan-1-ol: Experimental Selection Logic as a Monoprotected 1,4-Butanediol Building Block and a Protected C4 Linker

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Organic synthesis Medicinal Chemistry Hydroxyl Protecting Groups

三苯基膦参与的羧酸活化与酰胺键形成：活化路径、酸酐竞争与适用场景

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羧酸活化酰胺键形成

Triphenylphosphine-Involved Carboxylic Acid Activation and Amide Bond Formation: Activation Pathways, Anhydride Competition, and Applicability Scenarios

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Amide bond formation carboxylic acid activation

CMPI 在羧酸活化中的实验判断：适用任务、碱匹配与后处理负担

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有机合成羧酸活化 CMPI

Experimental Judgment for CMPI in Carboxylic Acid Activation: Applicable Tasks, Base Matching, and Workup Burden

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Organic synthesis carboxylic acid activation CMPI

TFPN 在羧酸活化中的实验判断：适用情形、中间体分布与亲核体适配

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羧酸活化酰胺键形成 TFPN

Experimental Judgment for TFPN in Carboxylic Acid Activation: Suitable Scenarios, Intermediate Distribution, and Nucleophile Compatibility

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carboxylic acid activation Amide bond construction TFPN

可见光催化在有机合成中的实验判断与条件选择

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光催化催化剂有机合成

Experimental Judgment and Condition Selection for Visible-Light Catalysis in Organic Synthesis

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Catalyst Photocatalyst Organic synthesis

小分子合成中的反应选择：从转化类型判断到实验路径筛选

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小分子合成

Reaction Selection in Small-Molecule Synthesis: From Transformation-Type Assessment to Experimental Route Screening

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Small-Molecule Synthesis

如何判断一个蛋白是否适合靶向降解：从降解通路、分子设计到机制验证

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蛋白质靶向蛋白降解靶向降解

How to Determine Whether a Protein Is Suitable for Targeted Degradation: From Degradation Pathway and Molecular Design to Mechanism Validation

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protein Targeted protein degradation Targeted degradation

复杂底物中低活性胺的选择性酰化：N/O 与 N/N 选择性控制思路

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酰胺键构建酰胺偶联复杂底物

Selective Acylation of Less Reactive Amines in Complex Substrates: Strategies for N/O and N/N Selectivity Control This article draws on the work of Li et al. on the TCFH/catalytic Oxyma system and transient imine protection, and summarizes design strateg

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Amide bond construction Amide coupling Complex substrates

多肽合成异常杂质如何排查？从氨基相关副反应看工艺问题定位

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多肽合成固相多肽合成异常杂质

How to Troubleshoot Abnormal Impurities in Peptide Synthesis? Locating Process Issues Through Amino-Related Side Reactions

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Peptide synthesis Solid phase peptide synthesis Abnormal impurities

多肽中间体难溶、难分离？标签辅助液相肽合成（TAG-LPPS）的路线设计与后处理策略

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多肽合成标签辅助液相肽合成多肽中间体

Peptide Intermediates Difficult to Dissolve and Separate? Route Design and Workup Strategies for Tag-Assisted Liquid-Phase Peptide Synthesis (TAG-LPPS)

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Peptide synthesis TAG-LPP Peptide Intermediates

AITF 介导羧酸活化用于酰胺、肽和酯合成：活化机制与适用场景

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酰胺键肽键酯键 AITF

AITF-Mediated Carboxylic Acid Activation for the Synthesis of Amides, Peptides, and Esters: Activation Mechanism and Applicable Scenarios

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Peptides AITF Amides Esters

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多肽合成

Formation and Control of Carboxyl- and Hydroxyl-Related Impurities in Peptide Synthesis — Using Asp/Glu and Ser/Thr Residue Side Reactions as Examples

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Peptide synthesis Functional Group Carboxyl group

桥头位 α-氟胺的稳定化设计及其药物化学砌块价值

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脂肪族胺氟原子

Stabilization Design of Bridgehead α-Fluoroamines and Their Value as Medicinal Chemistry Building Blocks

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Aliphatic amine Fluorine atom

CTSOBt 苯并三氮唑-磺酸酯缩合试剂：羧酸活化与合成应用价值

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多肽合成羧酸活化缩合试剂

CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value

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Peptide synthesis coupling reagent coupling reagents

氮杂三环烷烃的张力释放：三维氮杂桥环的桥位模块化官能团化与立体控制

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ABCAs 氮杂双环[x.1.1]烷烃

Strain Release of Azatricycloalkanes: Modular Bridge-Position Functionalization and Stereochemical Control of Three-Dimensional Bridged Aza Scaffolds

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ABCAs azabicyclo[x.1.1]alkanes

从光催化开环到骨架重构：氧杂环丁烷氧原子置换的反应逻辑与合成应用

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光催化骨架饱和四元环

From Photocatalytic Ring Opening to Skeletal Reconstruction: Reaction Logic and Synthetic Applications of Oxygen-Atom Replacement in Oxetanes

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Photocatalysts Saturated quaternary ring Skeleton

乙酰基四肽-2与弹性纤维形成：Fibulin-5、LOXL1及皮肤紧致相关研究

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化妆品

Acetyl Tetrapeptide-2 and Elastic Fiber Formation: Research on Fibulin-5, LOXL1, and Skin Firmness

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cosmetics

棕榈酰五肽-4如何作用于皮肤：从KTTKS序列、皮肤递送到胶原基质响应

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化妆品合成脂肽

How Palmitoyl Pentapeptide-4 Acts on the Skin: From the KTTKS Sequence and Skin Delivery to Collagen Matrix Responses

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Synthetic lipopeptides

环化如何改变多肽行为：以Cyclopeptide-5为例解析构象预组织、皮肤递送与整合素结合

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多肽护肤品

How Cyclization Changes Peptide Behavior: Conformational Preorganization, Skin Delivery, and Integrin Binding, Using Cyclopeptide-5 as an Example

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Polypeptide Skincare

1,8-萘啶型醛糖还原酶抑制剂：骨架构建、体外抑制活性与结构优化方向

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1,8-萘啶醛糖还原酶 ALR2 AKR1B1 醛糖还原酶抑制剂构效关系药效团苄位溴化

1,8-Naphthyridine-Based Aldose Reductase Inhibitors: Scaffold Construction, In Vitro Inhibitory Activity, and Directions for Structural Optimization

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ALR2 AKR1B1 1,8-naphthyridine aldose reductase aldose reductase inhibitor structure–activity relationship pharmacophore benzylic bromination

一级、二级胺为何难以直接参与经典Mitsunobu反应：BEHT介导醇胺化的机理、构型翻转与反应范围

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Mitsunobu反应 BEHT 质子化甜菜碱醇活化一级胺二级胺双分子亲核取代构型翻转 α-手性胺

Why Primary and Secondary Amines Have Difficulty Participating Directly in the Classical Mitsunobu Reaction: Mechanism, Inversion of Configuration, and Reaction Scope of BEHT-Mediated Alcohol Amination

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Mitsunobu Reaction BEHT Protonated Betaine Alcohol Activation Primary Amines Secondary Amines Bimolecular Nucleophilic Substitution Inversion Of Configuration Α-Chiral Amines

乙酰基六肽-8在表情纹管理中的作用基础：SNARE复合体干预、经皮递送限制与复配思路

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乙酰基六肽-8 阿基瑞林 SNAP-25 SNARE复合体表情纹透皮递送 A醇抗皱复配

Mechanistic Basis of Acetyl Hexapeptide-8 in the Management of Expression Lines: SNARE Complex Interference, Constraints on Percutaneous Delivery, and Combination Strategies

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Retinol SNAP-25 Acetyl Hexapeptide-8 Argireline SNARE complex expression lines transdermal delivery anti-wrinkle combinations

ImCl[H₂F₃]的储存稳定性与脱氧氟化反应性——H₂F₃⁻氟源反应性调控与2-氯咪唑鎓底物活化

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脱氧氟化

Storage Stability and Deoxyfluorination Reactivity of ImCl[H₂F₃]—Reactivity Modulation of the H₂F₃⁻ Fluoride Source and Substrate Activation by 2-Chloroimidazolium

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Deoxyfluorination

蓝铜胜肽 GHK-Cu 与皮肤修复：从铜配位化学到细胞外基质重塑

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细胞外基质 ECM GHK-Cu 皮肤修复

Copper Tripeptide GHK-Cu and Skin Repair: From Copper Coordination Chemistry to Extracellular Matrix Remodeling

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Extracellular matrix Skin Repair ECM GHK-Cu

从 DENV-2 筛选命中到四血清型覆盖：JNJ-1802 的泛血清型构效关系优化

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抑制剂 DENV-2 JNJ-1802

From a DENV-2 Screening Hit to Coverage of All Four Serotypes: Pan-Serotype Structure–Activity Relationship Optimization of JNJ-1802

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Inhibitors DENV-2 JNJ-1802

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7. Huiying Ding, Yuting Liu, Zhong Zhang, Yanjun Cheng, Jiahao Mo, Lu Elfa Peng, Cheng Xiang, Hongchang Pei, Xianhui Li. (2023) Regulation of interfacial polymerization by organic base for high-permselective nanofiltration. DESALINATION, [10.1016/j.desal.2023.117212]
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