2,2-Azobis(2-amidinopropane) dihydrochloride
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2,2-Azobis(2-amidinopropane) dihydrochloride
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CAS No:
2997-92-4
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Formula:
C8H18N6.2ClH
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Chemical Name:
2,2-Azobis(2-amidinopropane) dihydrochloride
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Synonyms:
Propanimidamide,2,2′-(1,2-diazenediyl)bis[2-methyl-,hydrochloride (1:2);Propionamidine,2,2′-azobis[2-methyl-,dihydrochloride;Propanimidamide,2,2′-azobis[2-methyl-,dihydrochloride;2,2′-Azobis(isobutyramidine hydrochloride);2,2′-Azobis(2-amidinopropane) dihydrochloride;Azobis(isobutyramidine) dihydrochloride;MS 1 (catalyst);MS 1;V 50;Azobisisobutyramidinium dichloride;2,2′-Azobisisobutyramidinium chloride;2,2′-Azobis(propane-2-carboxamidine) dihydrochloride;2,2′-Azobis(2-methylpropionamidine) dihydrochloride;2,2-Azobis(2-amidinopropane) dihydrochloride;Azostarter V 50;AAPH;2,2′-Azobisamidinopropane dihydrochloride;NC 32P;Vazo 56;VA 50;VA 50 (catalyst);AIBA;Wako V 50;Vazo 56WSP;Vazo 56WSW;2,2′-Azobis(isobutyramidine) dihydrochloride;VA 050;2,2′-Azodiisobutyramidine dihydrochloride;Azobis(isobutyl)amidine hydrochloride;TB 2000;TB 2000 (initiator);2,2′-Azodiisobutylamidine dihydrochloride;V 50 initiator;Vazo 55;2,2′-(Diazene-1,2-diyl)bis(2-methylpropanimidamide) dihydrochloride;DN 55549;4139-50-8;60345-43-9;89491-81-6;1904575-90-1
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CAS No:
2,2-Azobis(2-amidinopropane) dihydrochloride Basic Attributes
271.19
270.112640
221-070-0
7381JDR72F
DTXSID3049756
29270000
Characteristics
125
4.07180
White to off-white granular
0.42
165-170 °C (decomp)
267ºC at 760 mmHg
115.3ºC
acetone, dioxane, methanol, ethanol, DMSO and water: soluble
0-6°C
8.02E-05mmHg at 25°C
Oral-rat LD50: 410 mg/kg
Flammable; burning produces toxic nitrogen oxides and hydrogen chloride fumes
Safety Information
III
5.1
UN 3226 4.1
1
22-43-5
24-37
UE4575500
Xn
Ventilated, low temperature and dry; stored separately from food materials in warehouse
Unstable. Sensitive to heat and light. Incompatible with strong oxidizing agents, strong acids.
P280
H242-H302-H317
|Warning|H302: Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P272, P280, P301+P312, P302+P352, P321, P330, P333+P313, P363, and P501|H242 (33.77%): Heating may cause a fire [Danger Self-reactive substances and mixtures; Organic peroxides]|P210, P220, P234, P261, P264, P270, P272, P273, P280, P301+P312, P302+P352, P305+P351+P338, P321, P330, P333+P313, P337+P313, P363, P370+P378, P391, P403+P235, P411, P420, and P501|Aggregated GHS information provided by 385 companies from 12 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Electron-accepting molecules in chemical reactions in which electrons are transferred from one molecule to another (OXIDATION-REDUCTION). (See all compounds classified as Oxidants.)|Chemical agents that increase the rate of genetic mutation by interfering with the function of nucleic acids. A clastogen is a specific mutagen that causes breaks in chromosomes. (See all compounds classified as Mutagens.)
2,2'-azo-bis(2-amidinopropane)
2,2-Azobis(2-amidinopropane) dihydrochloride Use and Manufacturing
2,2'-Azobis[2-methyl-propanimidamide Dihydrochloride is used to prepare Resveratrol and its analogues for use as antioxidants. Also acts as an antioxidant.
Propanimidamide, 2,2'-(1,2-diazenediyl)bis[2-methyl-, hydrochloride (1:2): ACTIVE
Computed Properties
Molecular Weight:271.19
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:270.1126501
Monoisotopic Mass:270.1126501
Topological Polar Surface Area:125
Heavy Atom Count:16
Complexity:248
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes
Recommended Suppliers of 2,2-Azobis(2-amidinopropane) dihydrochloride
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2,2-Azobis(2-amidinopropane) dihydrochloride
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