跳转至内容
Merck
CN

T46108

1,2,4-三氮唑

98%

别名:

3,4-二氮杂吡咯, 4H-1,2,4-三唑, s-苯三唑(8CI)

登录 查看组织和合同定价。

选择尺寸

关于此项目

经验公式（希尔记法）:
C2H3N3
化学文摘社编号:
288-88-0
分子量:
69.07
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24900056
EC Number:
206-022-9
Beilstein/REAXYS Number:
104767
MDL number:
MFCD00005228

主要文件

查看所有文档
技术服务
需要帮助？我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助？我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

产品名称

1,2,4-三氮唑, 98%

InChI key

NSPMIYGKQJPBQR-UHFFFAOYSA-N

InChI

1S/C2H3N3/c1-3-2-5-4-1/h1-2H,(H,3,4,5)

SMILES string

c1nc[nH]n1

assay

98%

bp

260 °C (lit.)

mp

119-121 °C (lit.)

Quality Level

200

正在寻找类似产品? 访问 产品对比指南

相关类别

Application

1,2,4-三唑及其衍生物是许多药物的重要结构部分。三唑也可以作为配体与过渡金属离子形成配位化合物。由于缺电子，它们表现出优异的电子传输和空穴阻挡性能，使其成为材料科学应用中具有广阔前景的有机材料。

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Repr. 1B

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 2

flash_point_f

338.0 °F

flash_point_c

170 °C

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SDBB4545
STBL0726
44396KK
STBL2410
STBL2913

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

  3. How do I find price and availability?

    There are several ways to find pricing and availability for our products. Once you log onto our website, you will find the price and availability displayed on the product detail page. You can contact any of our Customer Sales and Service offices to receive a quote.  USA customers:  1-800-325-3010 or view local office numbers.

  4. What is the Department of Transportation shipping information for this product?

    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  5. What is the solubility of 1,2,4-Triazole (Product No. T46108)?

    Triazole is appreciably soluble in water and alcohol, according to the 14th edition of the chemicals encyclopedia published by the Royal Society of Chemistry.

  6. How is Product No. T46108, 1,2,4-Triazole, packaged?

    Product No. T46108 is typically packaged in a high density polyethylene (HDPE) bottle with a Teflon-lined polypropylene (PP) cap.

  7. How is Product No. T46108, 1,2,4-Triazole, produced?

    Typically the exact production methods are considered proprietary; this is also true for product T46108.  The 1,2,4-Triazole preparation is outlined in this article by C. Ainsworth: Org. Synth., 40, 99 (1960).

  8. What type of information is available for derivatives of 1,2,4-triazole (Product No. T46108)?

    A good source for information on 1,2,4-triazoles is a review article by K.T. Potts entitled The Chemistry of 1,2,4-Triazoles. Here is the citation: Chem. Rev., 61(2), 87-127 (1961).

  9. My question is not addressed here, how can I contact Technical Service for assistance?

    Ask a Scientist here.

1, 2, 4-Triazoles: Synthetic approaches and pharmacological importance.
Al-Masoudi IA
Chemistry of Heterocyclic Compounds, 42(11), 1377-1403 (2006)
Mononuclear, oligonuclear and polynuclear metal coordination compounds with 1, 2, 4-triazole derivatives as ligands.
Haasnoot JG
Coordination Chemistry Reviews, 200, 131-185 (2000)
Applications of Metal-Free 1, 2, 4-Triazole Derivatives in Materials Science.
Diaz-Ortiz A
Current Organic Chemistry, 19(7), 568-584 (2015)
Min Wang et al.
Chemical communications (Cambridge, England), 49(25), 2572-2574 (2013-02-21)
Enantioselective cyclization of α-isocyano esters with azodicarboxylates catalyzed by Fe(II)-N,N'-dioxide complexes has been developed. Under mild conditions, a variety of 1,2,4-triazoline derivatives was obtained in high yields and enantioselectivities.
Jing-Lin Chen et al.
Inorganic chemistry, 52(17), 9727-9740 (2013-08-22)
A new series of mononuclear copper(I) complexes (1-9) with functionalized 3-(2'-pyridyl)-1,2,4-triazole chelating ligands, as well as the halide and/or phosphine ancillary ligands, have been synthesized. Complexes 1-9 were fully characterized by elemental analysis, NMR spectroscopy, mass spectroscopy, electronic absorption spectroscopy
查看所有相关文献

我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持