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Home > Encyclopedia > 2,2-Azobis(2-amidinopropane) dihydrochloride

2,2-Azobis(2-amidinopropane) dihydrochloride

2,2-Azobis(2-amidinopropane) dihydrochloride structure

2,2-Azobis(2-amidinopropane) dihydrochloride 

structure
  • CAS No:

    2997-92-4

  • Formula:

    C8H18N6.2ClH

  • Chemical Name:

    2,2-Azobis(2-amidinopropane) dihydrochloride

  • 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

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

light yellow crystalline powder

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.

Toxicity

highly toxic

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

Uses

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

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