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Merck
CN

I3631

Isopentyl nitrite

Synonym(s):

Isoamyl nitrite

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About This Item

Linear Formula:
(CH3)2CHCH2CH2ONO
CAS Number:
110-46-3
Molecular Weight:
117.15
EC Number:
203-770-8
UNSPSC Code:
12171500
PubChem Substance ID:
24896040
Beilstein/REAXYS Number:
969510
MDL number:
MFCD00002057

Key Documents

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InChI key

OWFXIOWLTKNBAP-UHFFFAOYSA-N

InChI

1S/C5H11NO2/c1-5(2)3-4-8-6-7/h5H,3-4H2,1-2H3

SMILES string

CC(C)CCON=O

refractive index

n20/D 1.386 (lit.)

bp

99 °C (lit.)

density

0.872 g/mL at 25 °C (lit.)

storage temp.

2-8°C

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Other Notes

This product has been replaced by 150495-Sigma-Aldrich | Isopentyl nitrite 96%

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Muta. 2 - Skin Corr. 1B - Skin Sens. 1

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

-4.0 °F - closed cup

flash_point_c

-20 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
077K3662
126K3669
076K3663
036K3666
124K3735

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Analysis of alkyl nitrites by capillary gas chromatography-mass spectrometry.
T S Bal et al.
Journal - Forensic Science Society, 28(3), 185-190 (1988-05-01)
Hossein Mehrabi
Ultrasonics sonochemistry, 15(4), 279-282 (2007-10-26)
The reaction of 6-acylmethylphenanthridines with isoamyl nitrite results alpha-oximino-6-acylmethylphenanthridines in 73-95% yields in DMF under ultrasound irradiation. Compared with conventional methods, the main advantages of the present procedure are milder conditions, shorter reaction time and higher yields.
R M Uppu et al.
Analytical biochemistry, 236(2), 242-249 (1996-05-01)
A new method for the preparation of high concentrations of peroxynitrite (up to 1 M) is described. The synthesis uses a two-phase system and involves a displacement reaction by the hydroperoxide anion (in the aqueous phase) on isoamyl nitrite (in
The cycloaddition reaction of I(h)-Sc₃N@C₈₀ with 2-amino-4,5-diisopropoxybenzoic acid and isoamyl nitrite to produce an open-cage metallofullerene.
Guan-Wu Wang et al.
Angewandte Chemie (International ed. in English), 50(20), 4658-4662 (2011-04-16)
A Ahsan et al.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis, 6(3), 169-174 (2000-07-18)
Because the subcutaneous absorption of heparin depends on its molecular weight, high performance size exclusion chromatography methods, among others, have been developed for its determination. Because heparin consists of polymer chains of varying lengths, a large number of calibrators, 19
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