- Double-bond stereo
(E)-1,2-Diazenedicarboxamide
O=C(/N=N/C(=O)N)N CopyCopied
InChI=1S/C2H4N4O2/c3-1(7)5-6-2(4)8/h(H2,3,7)(H2,4,8)/b6-5+ CopyCopied
XOZUGNYVDXMRKW-AATRIKPKSA-N CopyCopied
Validated by Experts, Validated by Users, Non-Validated, Removed by Users, Redirected by Users, Redirect Approved by Experts
(E)-Diazene-1,2-dicarboxamide
1,2-diazenedicarboxamide, (E)-
ADA
(1E)-1-aminocarbonyliminourea
(E)-carbamoyliminourea
1,1'-Azobis(formamide)
1,1'-Azobisformamide
1,1'-Azodiformamide
123-77-3 [RN]
13682-92-3 [RN]
1758709
204-650-8 [EINECS]
208-797-9 [EINECS]
237-193-8 [EINECS]
247-530-0 [EINECS]
26239-55-4 [RN]
52737-71-0 [RN]
542-05-2 [RN]
62494-61-5 [RN]
62494-62-6 [RN]
62494-85-3 [RN]
65098-86-4 [RN]
65098-87-5 [RN]
72514-45-5 [RN]
73247-42-4 [RN]
73905-77-8 [RN]
76197-35-8 [RN]
81774-20-1 [RN]
89073-35-8 [RN]
97707-96-5 [RN]
ABFA
ADA NSC 674447
Azobiscarbonamide
Azobiscarboxamide
Azobisformamide
Azodicarboamide
azodicarbonamida [Portuguese]
Azodicarbonamide [Wiki]
Azodicarbonamide [UN3242] [Flammable solid]
azodicarbonamide;ADA NSC 674447
Azodicarboxamide
Azodicarboxylic acid diamide
AZODIFORMAMIDE
C,C'-Azodi(formamide)
Celogen AZ
Celogen AZ 130
Celogen AZ 199
Celosen AZ
ChKhz 21R
Diazene-1,2-dicarboxamide
Diazenedicarboxamide
Ficel EP-A
Formamide, 1,1'-azobis-
Genitron AC
Genitron AC 2
Genitron AC 4
Genitron EPC
Kempore
Kempore 125
Kempore 60/40
Kempore R 125
Lucel ADA
Nitropore
NSC-674447
Pinhole ACR 3
Pinhole AK 2
Poramid K 1
Porofor 505
Porofor adc/R
Porofor Chkhz 21
Porofor Chkhz 21R
Porofor DhKhZ 21
Porofor-lk 1074 (bayer)
Unifoam AZ
Unifoam AZH 25
Uniform AZ
Yunihomu AZ
δ(1,1')-Biurea
11621_FLUKA [DBID]
A96606_ALDRICH [DBID]
AI3-52516 [DBID]
CCRIS 842 [DBID]
ChKhz 21 [DBID]
HSDB 1097 [DBID]
NCGC00091844-01 [DBID]
NCI-C55981 [DBID]
NSC 41038 [DBID]
NSC 674447 [DBID]
UN3242 [DBID]
W504718_ALDRICH [DBID]
Data supplied by datasources and users.
Predicted data is generated using the ACD/Labs’ ACD/PhysChem Suite, for more information see their website.
Predicted data is generated using the US Environmental Protection Agency’s EPISuite™, for more information see their website.
Log Octanol-Water Partition Coef (SRC): Log Kow (KOWWIN v1.67 estimate) = -3.89 Log Kow (Exper. database match) = -1.70 Exper. Ref: VERSCHUEREN,K (1996) Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42): Boiling Pt (deg C): 312.74 (Adapted Stein & Brown method) Melting Pt (deg C): 117.02 (Mean or Weighted MP) VP(mm Hg,25 deg C): 1.02E-005 (Modified Grain method) MP (exp database): 212 dec deg C VP (exp database): 1.88E-10 mm Hg at 20 deg C Subcooled liquid VP: 1.33E-008 mm Hg (20 deg C, exp database VP ) Water Solubility Estimate from Log Kow (WSKOW v1.41): Water Solubility at 25 deg C (mg/L): 1.437e+005 log Kow used: -1.70 (expkow database) no-melting pt equation used Water Sol Estimate from Fragments: Wat Sol (v1.01 est) = 1e+006 mg/L ECOSAR Class Program (ECOSAR v0.99h): Class(es) found: Neutral Organics Henrys Law Constant (25 deg C) [HENRYWIN v3.10]: Bond Method : 3.41E-016 atm-m3/mole Group Method: Incomplete Henrys LC [VP/WSol estimate using EPI values]: 1.084E-011 atm-m3/mole Log Octanol-Air Partition Coefficient (25 deg C) [KOAWIN v1.10]: Log Kow used: -1.70 (exp database) Log Kaw used: -13.856 (HenryWin est) Log Koa (KOAWIN v1.10 estimate): 12.156 Log Koa (experimental database): None Probability of Rapid Biodegradation (BIOWIN v4.10): Biowin1 (Linear Model) : 0.6923 Biowin2 (Non-Linear Model) : 0.7958 Expert Survey Biodegradation Results: Biowin3 (Ultimate Survey Model): 2.9426 (weeks ) Biowin4 (Primary Survey Model) : 3.6803 (days-weeks ) MITI Biodegradation Probability: Biowin5 (MITI Linear Model) : 0.3668 Biowin6 (MITI Non-Linear Model): 0.3046 Anaerobic Biodegradation Probability: Biowin7 (Anaerobic Linear Model): 0.8361 Ready Biodegradability Prediction: NO Hydrocarbon Biodegradation (BioHCwin v1.01): Structure incompatible with current estimation method! Sorption to aerosols (25 Dec C)[AEROWIN v1.00]: Vapor pressure (liquid/subcooled): 1.77E-006 Pa (1.33E-008 mm Hg) Log Koa (Koawin est ): 12.156 Kp (particle/gas partition coef. (m3/ug)): Mackay model : 1.69 Octanol/air (Koa) model: 0.352 Fraction sorbed to airborne particulates (phi): Junge-Pankow model : 0.984 Mackay model : 0.993 Octanol/air (Koa) model: 0.966 Atmospheric Oxidation (25 deg C) [AopWin v1.92]: Hydroxyl Radicals Reaction: OVERALL OH Rate Constant = 2.0000 E-12 cm3/molecule-sec Half-Life = 5.348 Days (12-hr day; 1.5E6 OH/cm3) Half-Life = 64.176 Hrs Ozone Reaction: No Ozone Reaction Estimation Fraction sorbed to airborne particulates (phi): 0.988 (Junge,Mackay) Note: the sorbed fraction may be resistant to atmospheric oxidation Soil Adsorption Coefficient (PCKOCWIN v1.66): Koc : 33.4 Log Koc: 1.524 Aqueous Base/Acid-Catalyzed Hydrolysis (25 deg C) [HYDROWIN v1.67]: Rate constants can NOT be estimated for this structure! Bioaccumulation Estimates from Log Kow (BCFWIN v2.17): Log BCF from regression-based method = 0.500 (BCF = 3.162) log Kow used: -1.70 (expkow database) Volatilization from Water: Henry LC: 3.41E-016 atm-m3/mole (estimated by Bond SAR Method) Half-Life from Model River: 1.85E+012 hours (7.708E+010 days) Half-Life from Model Lake : 2.018E+013 hours (8.408E+011 days) Removal In Wastewater Treatment: Total removal: 1.85 percent Total biodegradation: 0.09 percent Total sludge adsorption: 1.75 percent Total to Air: 0.00 percent (using 10000 hr Bio P,A,S) Level III Fugacity Model: Mass Amount Half-Life Emissions (percent) (hr) (kg/hr) Air 8.12e-009 128 1000 Water 39 360 1000 Soil 60.9 720 1000 Sediment 0.0713 3.24e+003 0 Persistence Time: 579 hr
Click to predict properties on the Chemicalize site