CAS 2997-92-4

2,2-Azobis(2-amidinopropane) dihydrochloride

Description:

2,2-Azobis(2-amidinopropane) dihydrochloride, commonly referred to as AAPH, is a chemical compound that serves as a radical initiator in various polymerization processes. It is characterized by its ability to decompose thermally to generate free radicals, which can initiate chain reactions in the presence of suitable monomers. This compound is typically a white to off-white crystalline powder and is soluble in water, making it useful in aqueous systems. AAPH is often utilized in biochemical research, particularly in studies involving oxidative stress and the generation of reactive oxygen species. Its dihydrochloride form indicates the presence of two hydrochloride groups, which enhance its solubility and stability in solution. Safety considerations are important when handling AAPH, as it can be a potential irritant and should be managed with appropriate protective measures. Overall, AAPH is a valuable tool in both industrial applications and scientific research due to its radical-generating capabilities.

Formula: C₈H₁₈N₆·2ClH

InChI: InChI=1S/C8H18N6.2ClH/c1-7(2,5(9)10)13-14-8(3,4)6(11)12;;/h1-4H3,(H3,9,10)(H3,11,12);2*1H

InChI key: InChIKey=LXEKPEMOWBOYRF-UHFFFAOYSA-N

SMILES: C(N=NC(C(=N)N)(C)C)(C(=N)N)(C)C.Cl

Synonyms:

• 2,2'-Azobis(2-methylpropionamide)dihydrochloride
• 2,2'-Azobis(isobutyramidine hydrochloride)
• 2,2'-Azobis(propane-2-carboxamidine) dihydrochloride
• 2,2'-Azobis-(2-amidinopropane) dihydrochloride
• 2,2'-Azobis[2-Metilpropionamidina], Diclorhidrato
• 2,2'-Azobis[2-methylpropionamidin]dihydrochlorid
• 2,2'-Azobis[2-methylpropionamidine], dichlorhydrate
• 2,2'-Azobisamidinopropane dihydrochloride
• 2,2'-Azobisisobutyramidinium chloride
• 2,2-Azobis(2-Methylpropionamidine)Dihydrochlorid
• 2,2′-(Diazene-1,2-diyl)bis(2-methylpropanimidamide) dihydrochloride
• 2,2′-Azobis(isobutyramidine) dihydrochloride
• 2,2′-Azodiisobutylamidine dihydrochloride
• 2,2′-Azodiisobutyramidine dihydrochloride
• 2-(2-Amino-2-Imino-1,1-Dimethyl-Ethyl)Azo-2-Methyl-Propanamidine Dihydrochloride
• Aaph
• Aiba
• Azo two isobutyl Acetamiprid hydrochloride
• Azobis(isobutyl)amidine hydrochloride
• Azobis(isobutyramidine) dihydrochloride
• Azobisisobutyramidinium dichloride
• Azostarter V 50
• Dn 55549
• MS 1 (catalyst)
• Ms 1
• Nc 32P
• Propanimidamide, 2,2'-(1,2-diazenediyl)bis[2-methyl-, hydrochloride (1:2)
• Propanimidamide, 2,2'-azobis[2-methyl-, dihydrochloride
• Propionamidine, 2,2'-azobis[2-methyl-, dihydrochloride
• TB 2000 (initiator)
• Tb 2000
• V 50
• V 50 initiator
• V50
• VA 50 (catalyst)
• Va 050
• Va 50
• Vazo 55
• Vazo 56
• Vazo 56WSP
• Vazo 56WSW

Raltegravir Impurity 9 DiHCl

CAS: 2997-92-4

Formula: C₈H₁₈N₆·2HCl

Color and Shape: White To Off-White Solid

Molecular weight: 198.27 2*36.46

Ref: 4Z-R-2417

AAPH

CAS: 2997-92-4

AAPH: water-soluble azo, generates free radicals, used in lipid peroxidation studies, and antioxidation tests. Half-life ~175h at 37°C, pH neutral.

Formula: C₈H₂₀Cl₂N₆

Color and Shape: Solid

Molecular weight: 271.19

Ref: TM-T36175

2,2'-(Diazene-1,2-diyl)bis(2-methylpropanimidamide) dihydrochloride

CAS: 2997-92-4

Formula: C₈H₂₀Cl₂N₆

Purity: 98.0%

Color and Shape: Solid

Molecular weight: 271.19

Ref: 10-F079441

2,2'-Azobis[2-methyl-propanimidamide] Dihydrochloride

Controlled Product

CAS: 2997-92-4

Stability Hygroscopic, Light Sensitive
Applications 2,2'-Azobis[2-methyl-propanimidamide Dihydrochloride is used to prepare Resveratrol and its analogues for use as antioxidants. Also acts as an antioxidant.Also an impurity found in Colesevelam.
E0
References Fang, J. et al.: Chem. Eur. J., 8, 4191 (2002); Prior, R. et al.: J. Agri. Food Chem., 51, 3273 (2003);

Formula: C₈H₂₀Cl₂N₆

Color and Shape: Neat

Molecular weight: 271.19

Ref: TR-A932650

2,2'-(Diazene-1,2-diyl)bis(2-methylpropanimidamide) dihydrochloride

CAS: 2997-92-4

2,2'-(Diazene-1,2-diyl)bis(2-methylpropanimidamide) dihydrochloride (BPDC) is a synthetic compound that is used as an analytical reagent and a model system for oxidative injury. It has significant cytotoxicity on human cells in cell culture. BPDC induces oxidative damage to proteins and DNA by increasing the production of reactive oxygen species such as hydrogen peroxide, superoxide, and hydroxyl radicals. The mechanism of action is not well understood but may be due to Toll-like receptor signalling pathways. This compound has been shown to inhibit the activity of antioxidant enzymes such as glutathione peroxidase and catalase. It also inhibits the activity of proinflammatory cytokines such as IL-6 and IL-8. BPDC is being investigated for its potential use in bowel disease treatment.

Formula: C₈H₂₀Cl₂N₆

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 271.19 g/mol

Ref: 3D-FD142593

AAPH

CAS: 2997-92-4

Ref: BE-RMCR009008

Raltegravir Impurity 17

CAS: 2997-92-4

Formula: C₈H₁₈N₆(HCl)

Molecular weight: 198.27 : 2(36.46)

Ref: ST-EA-CP-R6032

2,2-Azobis(2-Methylpropionamidine) Dihydrochloride (AAPH) extrapure, 98%

CAS: 2997-92-4

Formula: C₈H₁₈N₆·2HCl

Purity: min. 98%

Color and Shape: White to off-white, Powder, Clear

Molecular weight: 271.19

Ref: SR-47138

2,2\'-Azobis[2-methyl-propanimidamide] Dihydrochloride

CAS: 2997-92-4

Formula: C₈H₁₈N₆(HCl)

Molecular weight: 198.27 : 2(36.5)

Ref: ST-EA-CP-C34018