| Identification | More | [Name]
tert-Butyl nitrite | [CAS]
540-80-7 | [Synonyms]
α，α-Dimethylethyl nitrite
NITROUS ACID TERT-BUTYL ESTER
T-BUTYL NITRITE
TERT-BUTYL NITRITE
TIMTEC-BB SBB007659
1,1-dimethylethylnitrite
2-methyl-2-nitritopropane
alpha,alpha-Dimethylethyl nitrite
alpha,alpha-dimethylethylnitrite
Nitrous acid, 1,1-dimethylethyl ester
Nitrous acid, t-butyl ester
nitrousacid,1,1-dimethylethylester
nitrousacid,t-butylester
tert-Butylnitrite,tech.90%
tert-Butyl nitrite, pure, 90%
t-Buthyl nitrite
2-methyl-2-propyl nitrite
TERT-BUTYL NITRITE: TECH., 90%
tert-Butyl nitrite, 90%, pure
Nitrous acid tert-butyl | [EINECS(EC#)]
208-757-0 | [Molecular Formula]
C4H9NO2 | [MDL Number]
MFCD00002055 | [Molecular Weight]
103.12 | [MOL File]
540-80-7.mol |
| Chemical Properties | Back Directory | [Appearance]
clear yellow liquid | [Boiling point ]
61-63 °C(lit.)
| [density ]
0.867 g/mL at 25 °C(lit.)
| [vapor pressure ]
13.466kPa at 25℃ | [refractive index ]
n20/D 1.368(lit.)
| [Fp ]
−10 °F
| [storage temp. ]
2-8°C
| [solubility ]
alcohol: very soluble(lit.) | [form ]
Liquid | [color ]
Clear yellow | [Water Solubility ]
slightly soluble | [Merck ]
14,1583 | [BRN ]
1209339 | [LogP]
2.24 at 20℃ | [CAS DataBase Reference]
540-80-7(CAS DataBase Reference) | [NIST Chemistry Reference]
(CH3)3CONO(540-80-7) |
| Safety Data | Back Directory | [Hazard Codes ]
F,Xn | [Risk Statements ]
R11:Highly Flammable.
R20/22:Harmful by inhalation and if swallowed . | [Safety Statements ]
S16:Keep away from sources of ignition-No smoking .
S24:Avoid contact with skin .
S46:If swallowed, seek medical advice immediately and show this container or label . | [RIDADR ]
UN 2351 3/PG 2
| [WGK Germany ]
1
| [RTECS ]
RA0802000
| [F ]
8 | [HazardClass ]
3 | [PackingGroup ]
II | [HS Code ]
29209085 |
| Hazard Information | Back Directory | [Chemical Properties]
clear yellow liquid | [Uses]
Jet propellant. | [General Description]
tert-Butyl nitrite (TBN) is an efficient NO source. TBN participates in photocatalyzed conversion of aryl- and heteroarylamines to selenides. It also participates in radical multifunctionalization reactions of aliphatic alkenes. | [Purification Methods]
If it is free from OH bands (IR) then distil it through a 12inch helices packed column under reduced pressure, otherwise wash with aqueous 5% NaHCO3 (effervescence), then H2O, dry (Na2SO4) and fractionate it through a 10 theoretical plates column at ca 10mm pressure. [Allen J Chem Soc 1968 1954, Coe & Doumani J Am Chem Soc 70 1516 1948, UV: Ungnade & Smiley J Org Chem 21 993 1956, IR: Terte Bull Soc Chim Belg 60 240 1951, Beilstein 1 IV 1622.] |
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