8.41689
Adipic dihydrazide
for synthesis
Synonym(s):
Adipic dihydrazide, Hexanedioic acid dihydrazide
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About This Item
Empirical Formula (Hill Notation):
C6H14N4O2
CAS Number:
Molecular Weight:
174.20
MDL number:
UNSPSC Code:
12352127
EC Index Number:
213-999-5
NACRES:
NA.22
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Quality Level
form
powder
autoignition temp.
360 °C
mp
178-182 °C
transition temp
flash point >150 °C
storage temp.
15-25°C
InChI
1S/C6H14N4O2/c7-9-5(11)3-1-2-4-6(12)10-8/h1-4,7-8H2,(H,9,11)(H,10,12)
InChI key
IBVAQQYNSHJXBV-UHFFFAOYSA-N
Application
<ul>
<li><strong>Comprehensive repair strategy in infected wound healing:</strong> Adipic dihydrazide is used in the formation of the GA/OKGM/MT hydrogel through a Schiff base reaction with modified gelatin (GA) to create an effective wound dressing with rapid hemostatic properties and the ability to promote fibroblast proliferation and migration, leading to accelerated wound healing (Qiu et al., 2024).</li>
<li><strong>Photothermally triggered shape memory polymers:</strong> Adipic dihydrazide was utilized in the cross-linking of porphyrin-based amphiphilic copolymer self-assemblies to create photothermally triggered one-component shape memory polymers, indicating potential for advanced material designs (Song et al., 2022).</li>
<li><strong>Alleviating osteoarthritis with hydrogels:</strong> Adipic dihydrazide is utilized in the formation of the HA/PRP/BM hydrogel through a Schiff base reaction with hyaluronic acid (HA), resulting in a self-healing hydrogel with properties tailored for cartilage protection and lubrication in the articular cavity (Zhou et al., 2022).</li>
</ul>
<li><strong>Comprehensive repair strategy in infected wound healing:</strong> Adipic dihydrazide is used in the formation of the GA/OKGM/MT hydrogel through a Schiff base reaction with modified gelatin (GA) to create an effective wound dressing with rapid hemostatic properties and the ability to promote fibroblast proliferation and migration, leading to accelerated wound healing (Qiu et al., 2024).</li>
<li><strong>Photothermally triggered shape memory polymers:</strong> Adipic dihydrazide was utilized in the cross-linking of porphyrin-based amphiphilic copolymer self-assemblies to create photothermally triggered one-component shape memory polymers, indicating potential for advanced material designs (Song et al., 2022).</li>
<li><strong>Alleviating osteoarthritis with hydrogels:</strong> Adipic dihydrazide is utilized in the formation of the HA/PRP/BM hydrogel through a Schiff base reaction with hyaluronic acid (HA), resulting in a self-healing hydrogel with properties tailored for cartilage protection and lubrication in the articular cavity (Zhou et al., 2022).</li>
</ul>
Analysis Note
Assay (HClO₄): ≥ 97,0 %(m)
Melting range (lower value): ≥ 178 °C
Melting range (upper value): ≤ 182 °C
Identity (IR): conforms
Melting range (lower value): ≥ 178 °C
Melting range (upper value): ≤ 182 °C
Identity (IR): conforms
hcodes
pcodes
Hazard Classifications
Aquatic Chronic 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
302.0 °F - closed cup
flash_point_c
150 °C - closed cup
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