structure of Amyl nitrate

Amyl nitrate

CAS No.: 1002-16-0
M. Wt: 133.14600
M. Fa: C5H11NO3
InChI Key: HSNWZBCBUUSSQD-UHFFFAOYSA-N
Appearance: Colorless To Light Yellow To Light Orange Liquid

Names and Identifiers of Amyl nitrate

CAS Number

1002-16-0

EC Number

213-684-2

IUPAC Name

pentyl nitrate

InChI

InChI=1S/C5H11NO3/c1-2-3-4-5-9-6(7)8/h2-5H2,1H3

InChIKey

HSNWZBCBUUSSQD-UHFFFAOYSA-N

Canonical SMILES

CCCCCO[N+](=O)[O-]

UNII

Z77A64H8TF

UN Number

1112

Physical and chemical properties of Amyl nitrate

Boiling Point

BP: 145 °C

Decomposition

When heated to decomposition it emits toxic fumes of /nitrogen oxides/.

Density

0.99

Exact Mass

133.07400

Flash Point

125 °F (open cup)

Index of Refraction

1.42

LogP

log Kow = 2.72 (est)

Melting Point

-190 °F (USCG, 1999)

Molecular Formula

C5H11NO3

Molecular Weight

133.14600

Odor

Sickening sweet odor

PSA

55.05000

Solubility

In water, 0.3%

Vapour Pressure

5.07 mm Hg at 25 °C

Water Solubility

Insoluble in water

Safety Information of Amyl nitrate

Pictograms

Signal Word

Warning

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

Applications of Amyl nitrate

Amyl nitrite has various applications:

  • Medical Use: Primarily prescribed for angina pectoris and as an antidote for cyanide poisoning.
  • Recreational Use: Commonly inhaled for its psychoactive effects, leading to its classification as a "party drug" or "poppers"—used for enhanced sexual experiences or euphoria.
  • Industrial Use: Employed as an additive in diesel fuels to improve ignition properties.

Interaction Studies of Amyl nitrate

Amyl nitrite interacts with several substances, which may enhance its pharmacological effects or increase the risk of adverse reactions:

  • Combining amyl nitrite with other vasodilators or alcohol can exacerbate hypotensive effects.
  • It may also interact with medications that affect heart rate or blood pressure.

Biological Activity of Amyl nitrate

Amyl nitrite acts as a potent vasodilator, causing relaxation of smooth muscles and expansion of blood vessels. This leads to decreased blood pressure and increased heart rate. Its therapeutic effects manifest rapidly upon inhalation, typically within one minute. Additionally, amyl nitrite serves as an antidote for cyanide poisoning by promoting the formation of methemoglobin, which binds cyanide to form non-toxic cyanmethemoglobin. Adverse effects may include hypotension, headache, dizziness, and methemoglobinemia—especially concerning for infants due to their physiological differences.

Physical sample testing spectrum (NMR) of Amyl nitrate

Physical sample testing spectrum (NMR) of Amyl nitrate

Retrosynthesis analysis of Amyl nitrate

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