Look at this if you want to make your own Hydrazine.
http://www.orgsyn.org/orgsyn/prep.asp?prep=cv1p0309 (http://www.orgsyn.org/orgsyn/prep.asp?prep=cv1p0309)
Hydrazine (N2H4) Sulphate
http://www.orgsyn.org/orgsyn/prep.asp?prep=cv5p0030 (http://www.orgsyn.org/orgsyn/prep.asp?prep=cv5p0030)
Reduction with Pd/C & N2H4
The Hydrazine, N2H4 is the hydrogen donor.
Hydrazine Hydrate(NH2NH2·H2O)
Compiled by Asheesh Kumar Jain
Synlett 2004, 2445-2446
(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_imgs/pdf.gif)
Introduction
The synthetic utilities of hydrazine hydrate have been extensively investigated in organic chemistry. Among reducing agents, hydrazine hydrate stands out for its application to a broad variety of reductive transformations.
It is easy to use and reduces many functional groups, such as carbonyl compounds, alkenes, alkynes
and nitro groups under mild reaction conditions. Hydrazine hydrate is commercially available. It is a liquid (mp –52 °C, bp 120–121 °C, d = 1.027 g/mL), and issoluble in water, ethanol, methanol, propanol and isobutanol.