Results for:
PubChem ID: 9321

Hydrazine

Compound Details

Synonymous names
HYDRAZINE
302-01-2
Diamine
Levoxine
Hydrazine base
Oxytreat 35
Diazane
Hydrazin
Hydrazyna
Hydrazine, anhydrous
Nitrogen hydride
Hydrazines
Hydrazine (anhydrous)
Hydrazyna [Polish]
RCRA waste number U133
Hydrazine anhydrous
CCRIS 335
Amerzine
HSDB 544
N2H4
H2NNH2
UNII-27RFH0GB4R
EINECS 206-114-9
27RFH0GB4R
CHEBI:15571
119775-10-9
DTXSID3020702
H 70 (FUEL)
NITROGEN HYDRIDE (N2H4)
HYDRAZINE (IARC)
HYDRAZINE [IARC]
HDZ
ISONIAZID IMPURITY E (EP IMPURITY)
ISONIAZID IMPURITY E [EP IMPURITY]
ALLOPURINOL IMPURITY F (EP IMPURITY)
ALLOPURINOL IMPURITY F [EP IMPURITY]
UN2029
UN3293
Hydrazine/Hydrazine sulfate
RCRA waste no. U133
Hydrazine Standard: N2H4 @ 100 mg/L in 1% Acetic Acid
Hydrazine Standard: N2H4 @ 1000 mg/L in 1% Acetic Acid
Diamidogen
Hidrazine
amino nitrogen
Zerox
Hydrazine fume
(anhydrous)
Catalyzed hydrazine
Scav-Ox II
HYDRAZINE (HYDRAZINE SULFATE)
Zerox (Salt/Mix)
Amerzine (Salt/Mix)
Diamine, hydrazine base
HYDRAZINE [MI]
HYDRAZINE [HSDB]
NH2NH2
Scav-Ox II (Salt/Mix)
HYDRAZINE [WHO-DD]
Hydrazine, anhydrous, 98%
Nitrogen hydride, (N2H4)
NH2-NH2
UN 2029 (Salt/Mix)
UN 2030 (Salt/Mix)
DTXCID30702
Hydrazine (hydrazine sulphate)
HYDRAZINE, (ANHYDROUS)
Catalyzed hydrazine (Salt/Mix)
CHEMBL1237174
HYDRAZINE AQUEOUS SOLUTION
DTXSID70159610
CREXVNNSNOKDHW-UHFFFAOYSA-N
MFCD00011417
STL281862
AKOS000269060
NCGC00188947-01
BP-13613
DB-007559
H0172
H0204
H0697
NS00014234
C05361
Q58447
J-017830
Q27110398
HZN
Microorganism:

No

IUPAC namehydrazine
SMILESNN
InchiInChI=1S/H4N2/c1-2/h1-2H2
FormulaH4N2
PubChem ID9321
Molweight32.046
LogP-1.5
Atoms2
Bonds0
H-bond Acceptor2
H-bond Donor2
Chemical Classificationnitrogen compounds hydrazines
CHEBI-ID15571
Supernatural-IDSN0260111

mVOC Specific Details

Boiling Point
DegreeReference
113.55 °C peer reviewed
Volatilization
A pKa of 7.96(1) indicates hydrazine will exist partially in the cation or anion form at pH values of 5 to 9 and, therefore, volatilization from water surfaces is not expected to be an important fate process(SRC). The Henry's Law constant for the neutral species of hydrazine is estimated as 6.07X10-7 atm-cu m/mole(SRC) derived from its vapor pressure, 14.4 mm Hg(2), and assigned value for water solubility of 1.0X10+6 mg/L (miscible)(3). This Henry's Law constant indicates that hydrazine is expected to be essentially nonvolatile from water and moist soil surfaces(4). With an air velocity at the liquid surface of 63.5 cm/sec, the volatilization of hydrazine from petri dishes containing 25%, 50% and 75% hydrazine-water mixtures was 0.5 g after 6.66 hr, about 1 g after 5 hr, and about 3 g after 5 hr, respectively(5). At each concentration, the rate of volatilization decreased with time(5). Hydrazine's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of hydrazine from dry soil surfaces may exist(SRC) based upon its vapor pressure(1).
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc of hydrazine can be estimated to be 13(SRC). According to a classification scheme(2), this estimated Koc value suggests that hydrazine is expected to have very high mobility in soil. The pKa of hydrazine is 7.92(3), indicating that this compound will exist partially in the cation form in the environment and cations generally adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(4). The nature and extent of hydrazine adsorption by clays and soils is very dependent on suspension pH and on the types of surface functional groups present on the solid matrix. Under acidic conditions, pH 4.0, 99.9% of the hydrazine is present as the protonated species and should be able to readily replace Na+ from exchange sites(3). Under alkaline conditions, pH 8.0, approximately 50% of the hydrazine is protonated and 50% is in neutral form. The primary mechanism of hydrazine adsorption in a montmorillonite clay suspension was cation exchange, both at pH 4 and 8; adsorption of hydrazine was lower at the higher pH value(3). The main mechanism for hydrazine retention at pH 4 and at low hydrazine concentrations in the upper Arrendondo soil horizon (fine sand) was also cation exchange. At higher concentrations more than 60% of the hydrazine interacted with a different type of binding site, possibly with organic-surface functional groups such as carbonyl groups(3). Under alkaline conditions, using upper horizon Arrendondo soil, (at pH 8.0) hydrazine was adsorbed more readily than at pH 4(3).
Vapor Pressure
PressureReference
12.2

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
Aspergillus FlavusKate et al. 2023
Aspergillus NigerKate et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
Aspergillus Flavusinoculated potato samplesGC-MSno
Aspergillus Nigerinoculated potato samplesGC-MSno