AZO-TERT-BUTANE

Product Name: AZO-TERT-BUTANE
CAS No.: 927-83-3
Chemical Name: AZO-TERT-BUTANE
Synonyms: VR-160;AZO-T-BUTANE;(tert-C4H9N)2;AZO-TERT-BUTANE;Azobis(t-butane);2,2'-Azoisobutane;Azobis-tert-butane;AZO-TERT-BUTANE 94%;Di-tert-butyldiazene;Bis(tert-butyl)diimine
CBNumber: CB7719725
Molecular Formula: C8H18N2
Formula Weight: 142.24
MOL File: 927-83-3.mol

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AZO-TERT-BUTANE Property

Melting point:: -14.5°C
Boiling point:: 47-48 °C8 mm Hg(lit.)
Density: 0.756 g/mL at 25 °C(lit.)
refractive index: n20/D 1.397(lit.)
Flash point:: 45 °F
storage temp.: 2-8°C
BRN: 1749274
InChI: 1S/C8H18N2/c1-7(2,3)9-10-8(4,5)6/h1-6H3
InChIKey: GKCPCPKXFGQXGS-UHFFFAOYSA-N
SMILES: CC(C)(C)N=NC(C)(C)C

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Safety

Hazard Codes: F,Xn
Risk Statements: 11-20/22-36/37/38
Safety Statements: 16-26-36
RIDADR: UN 1993 3/PG 2
WGK Germany: 3
F: 10
HS Code: 2927000090
Storage Class: 3 - Flammable liquids
Hazard Classifications: Acute Tox. 4 Oral
Eye Irrit. 2
Flam. Liq. 2
Skin Irrit. 2
STOT SE 3

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H225Highly Flammable liquid and vapour

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P233Keep container tightly closed.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 452106
Product name: 2,2′-Azobis(2-methylpropane)
Purity: 97%
Packaging: 5g
Price: $322
Updated: 2025/07/31

American Custom Chemicals Corporation

Product number: CHM0028460
Product name: AZO-T-BUTANE
Purity: 95.00%
Packaging: 5G
Price: $874.4
Updated: 2021/12/16

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AZO-TERT-BUTANE Chemical Properties,Usage,Production

Uses

2,2′-Azobis(2-methylpropane)(ABMP) serves as a photo initiator since it produces radicals when excited bythe photons. It is an easily available initiators.

Synthesis Reference(s)

Journal of the American Chemical Society, 95, p. 634, 1973 DOI: 10.1021/ja00783a080
Synthesis, p. 632, 1972 DOI: 10.1055/s-1972-21965

AZO-TERT-BUTANE Preparation Products And Raw materials

Raw materials

Preparation Products

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AZO-TERT-BUTANE Suppliers

China 29 Germany 2 Switzerland 1 United Kingdom 3 United States 4 Global 39

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927-83-3, AZO-TERT-BUTANERelated Search:

ABIN 2,2′-Azobis(2-methylpropionamidine) dihydrochloride 2,2'-Azobis(2,4-dimethyl)valeronitrile 2,2'-AZOBIS[2-METHYL-N-(2-HYDROXYETHYL)PROPIONAMIDE] 2,2'-AZOBIS(4-METHOXY-2,4-DIMETHYLVALERONITRILE) 1,1'-Azobis(cyanocyclohexane) 2,2'-Azodi(2-methylbutyronitrile) Dimethyl 2,2'-azobis(2-methylpropionate) 4,4'-Azobis(4-cyano-1-pentanol) AZO-TERT-BUTANE 2,2'-AZOBIS[2-(2-IMIDAZOLIN-2-YL)PROPANE] DIHYDROCHLORIDE 4,4'-Azobis(4-cyanovaleric acid) 2,2'-AZOBIS(N-BUTYL-2-METHYLPROPIONAMIDE) AZO-TERT-OCTANE 2,2'-AZOBIS[N-(2-PROPENYL)-2-METHYLPROPIONAMIDE] 2,2'-AZOBIS[2-(2-IMIDAZOLIN-2-YL)PROPANE] 2,2'-AZOBIS[2-(2-IMIDAZOLIN-2-YL)PROPANE] DISULFATE DIHYDRATE 2,2'-AZOBIS[2-METHYL-N-[1,1-BIS(HYDROXYMETHYL)-2-HYDROXYETHYL]PROPIONAMIDE]

(E)-1,2-Ditert-butyldiazene

(tert-C4H9N)2

1,2-Bis(1,1-dimethylethyl)diazene

1,1'-Azobis(1,1-dimethylethane)

Azobis-tert-butane

2,2′-Azobis(2-methylpropane),Azo-tert-butane, Di-tert-butyldiazene

2,2’-dimethyl-2,2’-azopropane

2,2'-Azo-2,2'-dimethylpropane

2,2'-Azoisobutane

Azobis(t-butane)

Azoethane, 1,1,1',1'-tetramethyl-

azoethane,1,1,1’,1’-tetramethyl-

bis(1,1-dimethylethyl)diazene

Bis(tert-butyl)diimine

Diazene, bis(1,1-dimethylethyl)-

diazene,bis(1,1-dimethylethyl)-

Di-tert-butyldiazene

VR-160

AZO-T-BUTANE

AZO-TERT-BUTANE

2,2'-AZOBIS(2-METHYLPROPANE)

AZO-TERT-BUTANE 94%

Azo-tert-butane, Di-tert-butyldiazene

Diazene, 1,2-bis(1,1-dimethylethyl)-

927-83-3

627-83-3

CH33CNNCCH33

Organic Building Blocks

Nitrogen Compounds

Azo/Diazo Compounds

Building Blocks

pharmacetical