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草酰二肼

规格或纯度: 97%

CAS编号: 996-98-5
分子式: C₂H₆N₄O₂
分子量: 118.09
Beilstein号: 1072110
EC号: 213-640-2
MDL号: MFCD00007608
PubChem编号: 13826

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货号 (SKU)	包装规格	是否现货	价格	数量
O107185-5g	5g	现货
O107185-25g	25g	现货
O107185-100g	100g	现货
O107185-500g	500g	现货

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共轭化学羰基化合物

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基本描述

规格或纯度	97%
英文名称	Oxalyldihydrazide
别名	草酸二酰肼，乙二酸二酰肼
英文别名	Oxalic dihydrazide
应用	乙二酰肼用作交联剂，用于富集微流体芯片内的羰基化蛋白质。它也被用来合成一系列新的锰和铁盐形成络合物模板缩合乙二醛。
储存温度	充氩
运输条件	常规运输
产品介绍	可溶于水，溶于乙醇、氯仿和二乙醚。Oxalyldihydrazide was used as a crosslinker for enrichment of carbonylated proteins within a microfluid chip. It was also used to synthesize a new series of manganese and iron salt forming complexes by template condensation with glyoxal. Oxalyldihydrazide was used as a crosslinker for enrichment of carbonylated proteins within a microfluid chip. It was also used to synthesize a new series of manganese and iron salt forming complexes by template condensation with glyoxal.

名称和标识符

EC号	213-640-2
IUPAC Name	ethanedihydrazide
INCHI	InChI=1S/C2H6N4O2/c3-5-1(7)2(8)6-4/h3-4H2,(H,5,7)(H,6,8)
InChi Key	SWRGUMCEJHQWEE-UHFFFAOYSA-N
Canonical SMILES	C(=O)(C(=O)NN)NN
分子式	C₂H₆N₄O₂
UN Number	2811
PubChem CID	13826
Beilstein号	1072110
分子量	118.09

化学和物理性质

溶解性	Solubility in hot Water:almost transparency
密度	1.461
敏感性	对空气敏感
熔点	239-243°C

安全信息

象形图	Environmental Hazard Harmful
信号词	Warning
危险声明	H315: Causes skin irritation H319: Causes serious eye irritation H411: Toxic to aquatic life with long lasting effects H317: May cause an allergic skin reaction
预防措施声明	P261,P305+P351+P338,P273,P280,P302+P352,P321,P501,P264,P272,P333+P313,P362+P364,P391,P264+P265,P337+P317,P332+P317
WGK Germany	3
RTECS	RO2840000
Reaxy-Rn	1072110
个人防护装备	Eyeshields,Gloves,type N95 (US),type P1 (EN143) respirator filter

参考文献

1. M Rizk,N A Zakhari,S S Toubar,Y el-Shabrawy. (1992-07-01) Sensitive colorimetric determination of copper (II) ions in some chemicals and multivitamins.. Acta pharmaceutica Hungarica, 62 ((4)): (158-166). [PMID:1442094]
2. Zahid H Chohan,M A Farooq,Andrea Scozzafava,Claudiu T Supuran. (2002-10-09) Antibacterial Schiff bases of oxalyl-hydrazine/diamide incorporating pyrrolyl and salicylyl moieties and of their zinc(II) complexes.. Journal of enzyme inhibition and medicinal chemistry, 17 ((1)): (1-7). [PMID:12365455]
3. Khlood Abou Melha. (2008-03-18) Antimicrobial, spectral, magnetic and thermal studies of Cu(II), Ni(II), Co(II), UO(2)(VI) and Fe(III) complexes of the Schiff base derived from oxalylhydrazide.. Journal of enzyme inhibition and medicinal chemistry, 23 ((2)): (285-295). [PMID:18343917]
4. D P Singh,Ramesh Kumar,Jitender Singh. (2008-05-20) Synthesis and spectroscopic studies of biologically active compounds derived from oxalyldihydrazide and benzil, and their Cr(III), Fe(III) and Mn(III) complexes.. European journal of medicinal chemistry, 44 ((4)): (1731-1736). [PMID:18486278]
5. Bryant C Hollins,Steven A Soper,June Feng. (2012-05-09) Enriching carbonylated proteins inside a microchip through the use of oxalyldihydrazide as a crosslinker.. Lab on a chip, 12 ((14)): (2526-2532). [PMID:22565136]
6. N Dhananjaya,H Nagabhushana,B M Nagabhushana,B Rudraswamy,S C Sharma,D V Sunitha,C Shivakumara,R P S Chakradhar. (2012-07-04) Effect of different fuels on structural, thermo and photoluminescent properties of Gd2O3 nanoparticles.. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 96 (): (532-540). [PMID:22750671]
7. Huanan Li,Yani Cui,Junhui Sui,Shaoquan Bian,Yong Sun,Jie Liang,Yujiang Fan,Xingdong Zhang. (2015-07-04) Efficient Delivery of DOX to Nuclei of Hepatic Carcinoma Cells in the Subcutaneous Tumor Model Using pH-Sensitive Pullulan-DOX Conjugates.. ACS applied materials & interfaces, 7 ((29)): (15855-15865). [PMID:26140410]
8. Z Deyl,M Adam,K Macek. (1981-08-14) 3-Hydroxypyridinium cross-links in lathyritic tissues.. Biochemical and biophysical research communications, 101 ((3)): (1026-1030). [PMID:7306105]
9. D P Singh,Ramesh Kumar,Jitender Singh. (2008-10-29) Antibacterial activity and spectral studies of trivalent chromium, manganese, iron macrocyclic complexes derived from oxalyldihydrazide and glyoxal.. Journal of enzyme inhibition and medicinal chemistry, 24 ((3)): (883-889). [PMID:18956272]

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