Azo-tert-butane
Basic information
- CAS
15464-01-4- Standard SMILES
CC(C)(C)N=NC(C)(C)C- InChIKey
GKCPCPKXFGQXGS-UHFFFAOYSA-N- Molecular formula
- C8H18N2
- Average molar mass
- 142.24 g/mol
- Monoisotopic mass
- 142.14699858
Names & identifiers
- Preferred name
- Azo-tert-butane
- IUPAC
- ditert-butyldiazene
- English name
- AZO-tert-butane
- Molecular formula
- C8H18N2
- Molecular weight
- 142.24
Names & synonyms
Azo-tert-butaneRefChem:560589627-515-9927-83-3Diazene, bis(1,1-dimethylethyl)-Azo-t-butaneDi-tert-butyldiazeneditert-butyldiazene2,2'-Azobis(2-methylpropane)2,2'-Azoisobutane1,2-Di-tert-butyldiazenetrans-Di-tert-butyldiazene
Show more names
VR-160(tert-C4H9N)2Azobis(t-butane)Azobis-tert-butaneAZO-TERT-BUTANE 94%
(E)-2,2'-AzoisobutaneAzoethane, 1,1,1',1'-tetramethyl-A8ML3TJS9515464-01-4Diazene, 1,2-bis(1,1-dimethylethyl)-Azoethane, 1,1,1',1'-tetramethyl-, (E)-Diazene, 1,2-bis(1,1-dimethylethyl)-, (1E)Bis(tert-butyl)diimine
Database identifiers
- CAS
15464-01-4、927-83-3- PubChem CID
- 70227
- DTXSID
DTXSID901346589- UNII
- A8ML3TJS95
- EC Number
- 627-515-9
- Nikkaji
- J80.014G
Properties
Computed structural properties
- XLogP
- 2.2
- Topological polar surface area
- 24.7 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 2
- Rotatable bonds
- 2
- Heavy atoms
- 10
- Formal charge
- 0
- Complexity
- 107
Physicochemical properties
- Melting point
- -14.5 °C · -14.5°C
- Boiling point
- 47 · 47-48 °C8 mm Hg(lit.)
- Density
- 0.756 g/mL · 0.756 g/mL at 25 °C(lit.)
- refractive index
- 20 · n20/D 1.397(lit.)
- Flash point
- 45 °F · 45 °F
- storage temp.
- 2 · 2-8°C
- BRN
- 1749274 · 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
- FDA UNII
- 8 ML3TJS95 · A8ML3TJS95
- UNSPSC Code
- 12352100 · 12352100
- NACRES
- 22 · NA.22
- Symbol(GHS)
- 2 · GHS02,GHS07
- Signal word
- Danger
- Hazard statements
- 225 · H225-H302+H332-H315-H319-H335
- Precautionary statements
- 210 · P210-P233-P301+P312-P303+P361+P353-P304+P340+P312-P305+P351+P338
- target organs
- Respiratory system
- PPE
- Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
- Hazard Codes
- F,Xn
- Risk Statements
- 11 · 11-20/22-36/37/38
- Safety Statements
- 16 · 16-26-36
- RIDADR
- 1993 · UN 1993 3/PG 2
- WGK Germany
- 3 · 3
- F
- 10 · 10
- HS Code
- 2927000090 · 2927000090
- Storage Class
- 3 · 3 - Flammable liquids
- Hazard Classifications
- 4 OralEye · Acute Tox. 4 OralEye Irrit. 2Flam. Liq. 2Skin Irrit. 2STOT SE 3
Safety & regulation
Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.
GHS classification
GHS Classification
Danger
H225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]
P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 39 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Hazard information
Hazard Classes and CategoriesFlam. Liq. 2 (100%)
Safety data
- F
- 10
- PPE
- Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
- wgk
- 3
- ridadr
- UN 1993 3/PG 2
- hs_code
- 2927000090
- risk_code
- 11-20/22-36/37/38
- Signal word
- Danger
- Symbol(GHS)
- GHS02,GHS07
- hazard_code
- F,Xn
- safety_code
- 16-26-36
- Storage Class
- 3 - Flammable liquids
- target organs
- Respiratory system
- Hazard statements
- H225-H302+H332-H315-H319-H335
- Hazard Classifications
- Acute Tox. 4 OralEye Irrit. 2Flam. Liq. 2Skin Irrit. 2STOT SE 3
- Precautionary statements
- P210-P233-P301+P312-P303+P361+P353-P304+P340+P312-P305+P351+P338
Chemistry & industry
Applications
Uses2,2′-Azobis(2-methylpropane)(ABMP) serves as a photo initiator since it produces radicals when excited bythe photons. It is an easily available initiators.
Upstream & downstream products
Downstream products
Related reactions
2 records
Compound notes
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