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13424-46-9

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13424-46-9 Usage

Uses

Different sources of media describe the Uses of 13424-46-9 differently. You can refer to the following data:
1. Lead azide [Pb(N3)2] is very unstable and must be handled with care. It is used as a detonator of explosives.
2. As primer in explosives. In the form of dextrinated lead azide.
3. Lead azide is used as a primary explosive indetonators and fuses to initiate the boosteror bursting charge. Generally, it is used indextrinated form. Lead azide is also used inshells, cartridges, and percussion caps.

Description

Lead azide is a severe explosion risk and should be handled under water; it is also a primary detonating compound.

Chemical Properties

needles or white powder(s); prepared by reaction of dilute solutions of lead nitrate and sodium azide; used as a primary detonating compound for high explosives; α-Pb(N3)2: orthorhombic, a=0.663nm, b=0.546 nm, c=1.625nm; β-Pb(N3)3: monoclinic, a=0.509 nm, b=0.884nm, c=1.751 nm; γ-Pb(N3)2: a=0.622nm, b=1.051 nm, c=1.217 nm [MER06] [CIC73] [KIR78]

Physical properties

Colorless needles or white powder; density ~4.0 g/cm3; explodes on heating at 350°C; slightly soluble in water, 230 mg/L at 18°C and 900 mg/L at 70°C; very soluble in acetic acid; insoluble in ammonia solution.

Production Methods

Different sources of media describe the Production Methods of 13424-46-9 differently. You can refer to the following data:
1. The percussion sensitivity of PbN6 led to its important use as a primer in munitions.
2. Lead azide crystallizes as colorless needles. It is a sensitive detonating agent, exploding at 350 °C. Lead azide is commonly prepared by the reaction between dilute solutions of lead nitrate and sodium azide. For safety, it is stirred vigorously to prevent formation of large crystals, which may detonate. Lead azide is usually precipitated with a protective material, such as gelatin, and then granulated. Lead azide is also used to prepare electrophotographic layers and for information storage on styrene–butadiene resins.

Preparation

Lead azide is prepared by the reaction of sodium azide with lead nitrate: 2NaN3 + Pb(NO3)2 → Pb(N3)2 + 2NaNO3.

General Description

Needles or white powder. Explodes at 350°C. Insoluble in water. May explode from shock, heat, flame or friction when dry. The primary hazard is the blast effect of an instantaneous explosion and not flying projectiles and fragments.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Lead azide is unstable. May, when dry, decompose explosively if shocked, heated or subjected to friction. Forms violently explosive products with carbon disulfide. Can be sensitized to explosive decomposition by metal salts (copper or zinc) or by traces of strong acids [Sax, 9th ed., 1996, p. 298]. An explosion occurred by mixing Lead azide with 0.5% of calcium stearate, [MCA Case History No. 949].

Hazard

Lead azide explodes on heating at 350°C or on percussion. Its detonation velocity is 5.1 km/sec (Meyer, E. 1989. Chemistry of Hazardous Materials, 2nd ed. Englewood Cliffs, N.J.: Prentice Hall). It undergoes violent explosive reaction with carbon disulfide and forms shock-sensitive copper and zinc azides when mixed with the solutions of copper and zinc salts (Patnaik, P. 1999. A Comprehensive Guide to the Hazardous Properties of Chemical Substances, 2nd ed. New York: John Wiley).

Health Hazard

Different sources of media describe the Health Hazard of 13424-46-9 differently. You can refer to the following data:
1. Fire may produce irritating, corrosive and/or toxic gases.
2. Toxicity data for lead azide are not available.Its aqueous solution is toxic, exhibitingpoisoning effect of lead.

Fire Hazard

MAY EXPLODE AND THROW FRAGMENTS 1600 meters (1 MILE) OR MORE IF FIRE REACHES CARGO.

Carcinogenicity

Results in an early study were deemed inconclusive because dose levels were not considered high enough. Rats were fed diets containing 100 or 200 ppm (6 or 12 mg/kg/day) sodium azide for 18 months followed by 6 months of observation. An increase in pituitary adenomas in the low-dose females compared to concurrent controls was found, but in this study the incidence in the control rats was unusually low compared to historical controls. A similar result occurred with mammary tumors.No carcinogenicity studies were found for hydrogen azide or lead azide but lead should be used as an analog for the latter chemical.

Waste Disposal

Lead azide is decomposed by treatment withnitrous acid or ceric ammonium nitrate (Wear1981).

Check Digit Verification of cas no

The CAS Registry Mumber 13424-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,2 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13424-46:
(7*1)+(6*3)+(5*4)+(4*2)+(3*4)+(2*4)+(1*6)=79
79 % 10 = 9
So 13424-46-9 is a valid CAS Registry Number.
InChI:InChI=1/4N3.Pb/c4*1-3-2;/q4*-1;+4

13424-46-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Lead(2+) diazide

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13424-46-9 SDS

13424-46-9Related news

Treatment of military primary explosives wastewater containing lead styphnate (LS) and Lead azide (cas 13424-46-9) (LA) by mFe0-PS-O3 process07/27/2019

Lead styphnate (C6H3N3O9Pb, LS) and lead azide (Pb(N3)2, LA) are identified to be the only viable replacements for mercury fulminate and widely used in various industries. However, the treatment of military explosive wastewater containing these pollutants was rarely reported currently. On one ha...detailed

13424-46-9Relevant articles and documents

Regularities of the formation of the photolysis products in the lead azide-cadmium system

Surovoi,Bugerko,Rasmatova

, p. 1151 - 1155 (2006)

Compared to PbN6(Ab), the PbN6(Ab)-Cd system was found to be characterized by a low photolysis rate within the region of intrinsic absorption of PbN6(Ab) and, at the same time, by a broader range of spectral sensitivity of PbN6(Ab), up to 510 nm. Preliminary irradiation by 380-nm light resulted in an increase in the photolysis rate. The photolysis rate constants for the PbN6(Ab)-Cd system were determined. An analysis of the voltammetric characteristics, photocurrent, and contact potential difference made it possible to develop a model of the photolysis of the PbN6(Ab)-Cd system, including the stages of generation, recombination, redistribution of nonequilibrium charge carriers in the contact field, the photoemission of electrons, formation of the photolysis products, and genesis of the PbN6(Ab)-Pb(photolysis product)-Cd system. It was demonstrated that the diffusion of anionic vacancies to neutral Pb n 0 sites is the limiting stage of the photolysis of the PbN 6(Ab)-Cd system. Nauka/Interperiodica 2006.

Hattori, K.,McCrone, W.

, p. 1791 - 1792 (1956)

PbII-catalyzed transformation of aromatic nitriles to heptanitrogen anions via sodium azide: a combined experimental and theoretical study

Huang, Rong-Yi,Zhang, Chao,Yan, Da,Xiong, Zhi,Xu, Heng,Ren, Xiao-Ming

, p. 39929 - 39936 (2018)

Under hydrothermal conditions, an open-chain N73? anion stabilized in a metal-organic framework (MOF) was achieved for the first time via the in situ reaction of 4-fluorobenzonitrile and sodium azide with Pb2+ ion as catalyst. The anion with C2h symmetry in the MOF was studied by FT-IR, single-crystal XRD and theoretical calculations. Thermal analysis results demonstrated the stability of the anion in the MOF below 430 °C and a high energy content of 8.61 kJ g?1. The anion is also a good reducing agent. It can easily react with basic KMnO4 solution. Moreover, the present study indicates that the Pb2+ ion activates the azide rather than nitrile in the in situ reaction of nitriles with azides to form polynitrogen and this mechanism is a distinct contradiction with the previous results in which the nitrile reacts with azide in the presence of transition metal ions. Our findings may open a new avenue towards the synthesis and capture of polynitrogen compounds.

Kinetics of the formation of photolysis products in the lead azide-cadmium telluride systems

Surovoi,Bugerko,Rasmatova

, p. 981 - 985 (2007/10/03)

The kinetic and spectral regularities of the formation of the gaseous (nitrogen) and solid-phase (lead) products of the photolysis of lead azide in contact with cadmium telluride at different intensities of the incident light with λ = 380 nm were investigated by mass spectrometry and spectrophotometry. Rate constants of the photolysis of PbN6(Ab)-CdTe systems were determined. It was shown that, during the formation of PbN 6(Ab)-CdTe systems, the photolysis rate in the absorption region of PbN6(Ab) is decreased, and the region of spectral sensitivity of lead azide is broadened. Based on a consideration of measured current-voltage characteristics, photocurrent and photo-emf values, and contact potential differences, a model of the photolysis of PbN6(Ab)-CdTe systems was proposed. The model involves the stages of generation, recombination, and redistribution of nonequilibrium carriers in the contact field, formation of the photolysis products, and also formation of PbN6(Ab)-Pb (photolysis product)-CdTe heterogeneous systems. Copyright

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