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

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为什么选择此级别

提供 ≥97% 纯度，适用于对基线干扰要求严格的色谱和分析工作流程。

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储存与运输

-20°C储存,充氩。超低温运输。请查阅批次 COA 获取详细规格。

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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。

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文献证明

在色谱分析、有机合成和交叉偶联反应领域已被 80 篇同行评审文献引用。

概述

用作溶液和固相肽合成中的羧酸的活化剂；性能优于或相当于最畅销的偶联剂。

应用

4-(4,6-二甲氧基-1,3,5-三嗪-2-基)-4-甲基吗啉盐酸盐可用作以下转化反应的缩合剂：
羧酸和胺在四氢呋喃中发生缩合反应，产生相应的酰胺。
羧酸与醇的酯化反应，产生相应的酯。
在质子溶剂中，将羧酸转化为相应的Weinreb酰胺。

Reagent for activating carboxylic acids in solution and solid phase peptide synthesis; superior or comparable to the most popular coupling reagents.

规格

别名

4-(4,6-二甲氧基三嗪-2-基)-4-甲基吗啉鎓氯化物水合物

英文别名

MMTM | DMTMM | 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-ium chloride hydrate

规格或纯度

≥97%

英文名称

4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride hydrate（DMTMM）

储存条件

-20°C储存,充氩

运输条件

超低温运输

纯度

≥97%

名称和识别符

PubChem SID

528759690

EC号

447-230-1

分子类型

小分子

IUPAC Name

4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-ium;chloride

INCHI

1S/C10H17N4O3.ClH/c1-14(4-6-17-7-5-14)8-11-9(15-2)13-10(12-8)16-3;/h4-7H2,1-3H3;1H/q+1;/p-1

InChi Key

BMTZEAOGFDXDAD-UHFFFAOYSA-M

Smiles

C[N+]1(CCOCC1)C2=NC(=NC(=N2)OC)OC.[Cl-]

Isomeric SMILES

C[N+]1(CCOCC1)C2=NC(=NC(=N2)OC)OC.[Cl-]

关联CAS

293311-01-0

UN Number

3261

Packing Group

分子量

276.72(anhy)

Beilstein号

8026872

Reaxy-Rn

8026872

Reaxys-RN link address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8026872&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) 有机杂环化合物
  - 类（Class) 三嗪类
    - 亚类（Subclass） 1,3,5-三嗪
      - 第5级 (level 5) 烷氧基-S-三嗪
        第6级 (level 6) 2-甲氧基-1,3,5-三嗪

界（kingdom)	有机化合物
超类（Superclass)	有机杂环化合物
类（Class)	三嗪类
亚类（Subclass）	1,3,5-三嗪
中间层级节点（Intermediate Tree Nodes）	烷氧基-S-三嗪
直接上位类(Direct Parent)	2-甲氧基-1,3,5-三嗪
其他上位类（Alternative Parents）	氨基三嗪类烷基芳基醚吗啉杂芳族化合物氧环化合物二烷基醚氮杂环化合物有机光子化合物有机氮化合物有机氯化物盐碳氢化合物衍生物
分子骨架（Molecular Framework)	芳香族杂单环化合物
取代基（Substituents）	2-methoxy-1,3,5-triazine - 芳基醚 - 氨基-1,3,5-三嗪 - 氨基三嗪 - 芳香族杂单环化合物 - 氮杂环 - 二烷基醚 - 乙醚 - 杂芳香族化合物 - 烃衍生物 - Morpholine - 有机氯酸盐 - 有机硝基化合物 - 有机氧化合物 - 有机盐 - 有机氮化合物 - 有机氧化合物 - 有机氮化合物 - 氧杂环 - 氧杂吡嗪烷
描述（Description）	该化合物属于有机化合物中的2-甲氧基-1,3,5-三嗪类。这类芳香杂环化合物含有1,3,5-三嗪环，其2位被甲氧基取代。
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

溶解性

Soluble in water, Methanol

密度

1.007

敏感性

对热敏感；对湿度敏感；对空气敏感

闪点(℉)

197.6 °F

闪点(℃)

92 °C

熔点

110-114°C

分子量

276.720 g/mol

XLogP3

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

276.099 Da

单同位素质量Monoisotopic Mass

276.099 Da

拓扑极表面积Topological Polar Surface Area

66.400 Å²

重原子数Heavy Atom Count

形式电荷Formal Charge

复杂度Complexity

236.000

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）

象形图

GHS05, GHS07

信号词

危险

危险声明

H302: 吞食有害

H314: 造成严重的皮肤灼伤和眼睛损伤

预防措施声明

P260: 不要吸入灰尘/烟雾/气体/雾/蒸汽/喷雾。

P264: 处理后要彻底洗手。

P270: 使用本产品时，请勿进食、饮水或吸烟。

P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。

P321: 特殊处理（请参阅此标签上的...）。

P330: 漱口

P363: 再次使用之前，请清洗受污染的衣物。

P301+P330+P331: 如误吞咽：漱口。不要诱导呕吐。

P304+P340: 如误吸入：将人转移到空气新鲜处，保持呼吸舒适体位。

P405: 密闭存放

P501: 将内容物/容器处理到。。。

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。

P302+P361+P354: 如果接触皮肤：立即脱掉所有被污染的衣服。立即用水冲洗几分钟。

P316: 立即寻求紧急医疗救助。

WGK Germany

Class

个人防护装备

Eyeshields,Faceshields,full-face particle respirator type N100 (US),Gloves,respirator cartridge type N100 (US),type P1 (EN143) respirator filter,type P3 (EN 143) respirator cartridges

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46个结果

批号(Lot Number)	证书类型	货号
F2611108	分析证书	D110326
C2620372	分析证书	D110326
C2620381	分析证书	D110326
C2620382	分析证书	D110326
C2620383	分析证书	D110326
J2509331	分析证书	D110326
I2604116	分析证书	D110326
J2509328	分析证书	D110326
J2509329	分析证书	D110326
J2509330	分析证书	D110326
J2408334	分析证书	D110326
J2408335	分析证书	D110326
J2408336	分析证书	D110326
J2408337	分析证书	D110326
G2518016	分析证书	D110326
E2530066	分析证书	D110326
D2525047	分析证书	D110326
E2509225	分析证书	D110326
C2429435	分析证书	D110326
C2429424	分析证书	D110326
C2409203	分析证书	D110326
C2409198	分析证书	D110326
C2409199	分析证书	D110326
C2409200	分析证书	D110326
C2409201	分析证书	D110326
C2409202	分析证书	D110326
G2425053	分析证书	D110326
C2409205	分析证书	D110326
F2417085	分析证书	D110326
I2318091	分析证书	D110326
I2318096	分析证书	D110326
I2318102	分析证书	D110326
I2318105	分析证书	D110326
I2318128	分析证书	D110326
F23161098	分析证书	D110326
F23161097	分析证书	D110326
F23161091	分析证书	D110326
F23161090	分析证书	D110326
F23171147	分析证书	D110326
I2220424	分析证书	D110326
I2220423	分析证书	D110326
I2220422	分析证书	D110326
I2220275	分析证书	D110326
E2322586	分析证书	D110326
C1809025	分析证书	D110326
C1827092	分析证书	D110326

显示更多⌵

技术文档和文章

连接蛋白质科学的桥梁——阿拉丁@多肽

目录：技术文章

探索主题:

药物开发偶联多肽合成试剂多肽蛋白质科学

A bridge to protein science——Aladdin@Polypeptide

目录：技术文章

探索主题:

Drug development Conjugated Peptide synthesis reagent Polypeptide Protein Science

三嗪类化合物：结构特征、分类逻辑、典型应用与科研选型要点

目录：技术文章

探索主题:

含氮杂环三嗪三嗪类化合物

Triazine Compounds: Structural Features, Classification Logic, Typical Applications, and Key Considerations for Research Selection

目录：技术文章

探索主题:

Nitrogen-containing heterocycles Triazine Triazine Compounds

β-酰氧基烯基酰胺（AAAs）：一种值得关注的酰胺键与肽键构建新思路

目录：技术文章

探索主题:

AAAs β-酰氧基烯基酰胺

β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention

目录：技术文章

探索主题:

AAAs β-Acyloxy Alkenyl Amides

从高活性到综合评价：以 CTSOAt 为例看新型缩合试剂的设计思路

目录：技术文章

探索主题:

新型缩合试剂

From High Reactivity to Comprehensive Evaluation: Using CTSOAt as an Example to Understand the Design Logic of New Coupling Reagents

目录：技术文章

探索主题:

New Coupling Reagents

TCFH–NMI 在高含水体系中的酰胺化：研究价值、方法认识与实验启示

目录：技术文章

探索主题:

酰胺键构建酰胺化反应 TCFH–NMI

TCFH–NMI Amidation in Highly Aqueous Media: Research Value, Methodological Understanding, and Experimental Insights

目录：技术文章

探索主题:

Amidation reaction TCFH–NMI Amide bond construction

缩合试剂的新平衡：DMT-TU 如何平衡反应活性、消旋控制与热危险性

目录：技术文章

探索主题:

有机合成酰胺键构建缩合试剂多肽化学

A New Balance in Coupling Reagents: How DMT-TU Balances Reactivity, Racemization Control, and Thermal Hazard

目录：技术文章

探索主题:

Organic synthesis Amide bond construction condensing reagent Peptide Chemistry

TBTU 的应用定位：消旋风险、延伸用途与选用判断

目录：技术文章

探索主题:

酰胺键构建羧酸活化 TBTU

The Positioning of TBTU in Practice: Racemization Risk, Extended Uses, and Selection Criteria

目录：技术文章

探索主题:

carboxylic acid activation Amide bond construction TBTU

从“高收率”到“保构型”：缩合体系的活化阶段风险、路线差异与选用思路

目录：技术文章

探索主题:

多肽合成手性酰胺

From “High Yield” to “Configuration Retention”: Activation-Stage Risks, Route Differences, and Selection Principles for Coupling Systems

目录：技术文章

探索主题:

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

目录：技术文章

探索主题:

HATU

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

目录：技术文章

探索主题:

HATU

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

目录：技术文章

探索主题:

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

目录：技术文章

探索主题:

Peptide synthesis Amide bond construction Racemic

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

目录：技术文章

探索主题:

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

目录：技术文章

探索主题:

Amide bond formation condensing reagent Amide bond

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

目录：技术文章

探索主题:

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)

目录：技术文章

探索主题:

Peptide synthesis TAG-LPP Peptide Intermediates

含水介质中酰胺化试剂的选择逻辑：竞争反应、活化中间体与底物效应

目录：技术文章

探索主题:

酰胺化反应

Logic for Selecting Amidation Reagents in Aqueous Media: Competing Reactions, Activated Intermediates, and Substrate Effects

目录：技术文章

探索主题:

Amidation reaction

吗啉类中间体如何选型？从连接位点、目标键型到合成路线设计

目录：技术文章

探索主题:

吗啉吗啉类中间体

How to Select Morpholine Intermediates: From Connection Sites and Target Bond Types to Synthetic Route Design

目录：技术文章

探索主题:

Morpholine Morpholine Intermediates

此产品的引用文献

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引用文献

1. Yao Chen, Miner Hu, Honghua Hu, Shunxian Ji, Leyi Huang, Wei Wei, Kun Zhao, Chong Teng. (2023) Fabrication of an Adhesive Small Intestinal Submucosa Acellular Matrix Hydrogel for Accelerating Diabetic Wound Healing. ACS Omega, [PMID:38107900] [10.1021/acsomega.3c05682]
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5. Zhang Peisen, Cheng Junwei, Lu Yijie, Zhang Ni, Wu Xiaoai, Lin Hua, Li Wei, Wang Jian, Winnik Mitchell A., Gan Zhihua, Hou Yi. (2023) Hypersensitive MR angiography based on interlocking stratagem for diagnosis of cardiac-cerebral vascular diseases. Nature Communications, 14 (1): (1-19). [PMID:37783733] [10.1038/s41467-023-41783-9]
6. Huangrong Zhu, Fengling Liu, Xinrang Zhai, Zhicheng Tong, Huimin Li, Wei Dong, Wei Wei, Chong Teng. (2023) Revisiting matrix hydrogel composed of gelatin and hyaluronic acid and its application in cartilage regeneration. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, [PMID:37774575] [10.1016/j.bbrc.2023.09.060]
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11. Jing Ni, Mengdi Li, Chaolun Li, Zhe Zhong, Hongwei Xi, Yiqun Wu. (2023) Stem-cell based soft tissue substitutes:engineering of cross-linked polylysine-hyaluronic acid microspheres ladened with gingival mesenchymal stem cells for collagen tissue regeneration and angiogenesis. JOURNAL OF PERIODONTOLOGY, [PMID:37133980] [10.1002/JPER.22-0747]
12. Saijun Wang, Zaigang Zhou, Rui Hu, Mingyue Dong, Xiaobo Zhou, Siyan Ren, Yi Zhang, Chengxun Chen, Ruoyuan Huang, Man Zhu, Wanying Xie, Ling Han, Jianliang Shen, Congying Xie. (2023) Metabolic Intervention Liposome Boosted Lung Cancer Radio-Immunotherapy via Hypoxia Amelioration and PD-L1 Restraint. Advanced Science, [PMID:37092578] [10.1002/advs.202207608]
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