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Oxalyldihydrazide - 97%, high purity , CAS No.996-98-5

≥97%

CAS#: 996-98-5
Formula: C₂H₆N₄O₂
Molecular Weight: 118.09
Beilstein Registry Number: 1072110
EC Number: 213-640-2
MDL number: MFCD00007608
PubChem CID: 13826
PubChem SID: 488181906

Item Number

O107185

Grouped product items
SKU	Size	Availability	Price
O107185-5g	5g	In stock	$12.90
O107185-25g	25g	In stock	$49.90
O107185-100g	100g	In stock	$178.90
O107185-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$801.90

View related series

Carbonyl compound Conjugation chemistry

Basic Description

Synonyms	Oxalyl dihydrazide\|996-98-5\|Ethanedihydrazide\|Oxalyldihydrazide\|Oxalic dihydrazide\|Ethanedioic acid, dihydrazide\|Oxaldihydrazide\|Oxalyl hydrazide\|Oxalhydrazide\|Oxalylhydrazine\|Oxaloylhydrazine\|Oxalic hydrazide\|Oxaloyl dihydrazide\|Oxalohydrazide\|Oxaloylhyd
Specifications & Purity	97%
Storage Temp	Argon charged
Shipped In	Normal
Product Description	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.

Names and Identifiers

Pubchem Sid	488181906
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488181906
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
Isomeric SMILES	C(=O)(C(=O)NN)NN
WGK Germany	3
RTECS	RO2840000
PubChem CID	13826
UN Number	2811
Molecular Weight	118.09
Beilstein	1072110
Reaxy-Rn	1072110

Certificates

Certificate of Analysis(COA)

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12 results found

Lot Number	Certificate Type	Date	Item
K2009127	Certificate of Analysis	Aug 16, 2024	O107185
H2307284	Certificate of Analysis	Jun 29, 2023	O107185
H2307293	Certificate of Analysis	Jun 29, 2023	O107185
F2302261	Certificate of Analysis	May 16, 2023	O107185
F2302262	Certificate of Analysis	May 16, 2023	O107185
F2302263	Certificate of Analysis	May 16, 2023	O107185
F2302264	Certificate of Analysis	May 16, 2023	O107185
F2302265	Certificate of Analysis	May 16, 2023	O107185
F2302266	Certificate of Analysis	May 16, 2023	O107185
F2302267	Certificate of Analysis	May 16, 2023	O107185
B2311338	Certificate of Analysis	Aug 23, 2021	O107185
B2311341	Certificate of Analysis	Aug 23, 2021	O107185

Solubility

Solubility in hot Water:almost transparency

Sensitivity

air sensitive

Melt Point(°C)

239-243°C

Safety and Hazards(GHS)

Pictogram(s)	GHS09, GHS07
Signal	Warning
Hazard Statements	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
Precautionary Statements	P261:Avoid breathing dust/fume/gas/mist/vapors/spray. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing. P273:Avoid release to the environment. P280:Wear protective gloves/protective clothing/eye protection/face protection. P302+P352:IF ON SKIN: wash with plenty of water. P321:Specific treatment (see ... on this label). P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P272:Contaminated work clothing should not be allowed out of the workplace. P333+P313:IF SKIN irritation or rash occurs: Get medical advice/attention. P362+P364:Take off contaminated clothing and wash it before reuse. P391:Collect spillage. P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes. P337+P317:If eye irritation persists: Get medical help. P332+P317:If skin irritation occurs: Get medical help.
WGK Germany	3
RTECS	RO2840000
Reaxy-Rn	1072110

References

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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