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100-47-0

Benzonitrile

CAS: 100-47-0

Molecular Formula: C7H5N

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100-47-0 - Names and Identifiers

Name Benzonitrile
Synonyms BN
BRR
2BNC
Hsdb 45
Nsc 8039
Ai3-24184
Ccris 3184
Benzontrile
Fenylkyanid
Benzoitrile
Benzonitrile
Cyanobenzene
Phenylcyanide
Phenyl cyanide
Benzenenitrile
PHENYL CYANIDE
Benzene, cyano-
PHENYLMETHANITRILE
Benzenecarbonitrile
Benzoic acid nitrile
BENZONITRILE OEKANAL, 250 ML
CAS 100-47-0
EINECS 202-855-7
InChI InChI:1S/C7H5N/c8-6-7-4-2-1-3-5-7/h1-5H
InChIKey JFDZBHWFFUWGJE-UHFFFAOYSA-N

100-47-0 - Physico-chemical Properties

Molecular FormulaC7H5N
Molar Mass103.12
Density1.01
Melting Point-13 °C (lit.)
Boling Point191 °C (lit.)
Flash Point161°F
Water Solubility10 g/L (100 ºC)
Solubility 10g/l
Vapor Presure1 hPa at 20 °C
Vapor Density3.6 (vs air)
AppearanceLiquid
ColorClear colorless to slightly yellow
OdorAlmond-like.
Exposure LimitNIOSH: IDLH 14 ppm(25 mg/m3)
Maximum wavelength(λmax)['λ: 300 nm Amax: 1.0',
, 'λ: 310 nm Amax: 0.40',
, 'λ: 335 nm Amax: 0.03',
, 'λ: 360
Merck14,1097
BRN506893
Storage ConditionStore below +30°C.
StabilityStable. Incompatible with strong bases, strong acids, strong oxidizing agents, strong reducing agents. Air-sensitive. Combustible.
Explosive Limit1.4-7.2%(V)
Refractive Indexn20/D 1.528(lit.)
Physical and Chemical PropertiesColorless oily liquid. There is bitter almond odor, bitter taste.
melting point -13 ℃
boiling point 190.7 ℃
relative density 1.0102
refractive index 1.5289
solubility slightly soluble in cold water, 100 ° C in water solubility of 1%; Miscible with commonly used organic solvents.
UseUsed as pesticides, dye intermediates and solvent antioxidants

100-47-0 - Risk and Safety

Hazard SymbolsXn - Harmful
Harmful
Risk CodesR21/22 - Harmful in contact with skin and if swallowed.
R38 - Irritating to the skin
Safety Description23 - Do not breathe vapour.
UN IDsUN 2224 6.1/PG 2
WGK Germany2
RTECSDI2450000
TSCAYes
HS Code29269090
Hazard Class6.1
Packing GroupII
ToxicityLDLo orl-rat: 720 mg/kg AMRL** TR-74-78,74

100-47-0 - Upstream Downstream Industry

Raw MaterialsToluene
Ammonia
Downstream Products3-Nitrobenzonitrile

100-47-0 - Nature

Open Data Verified Data

colorless transparent liquid. There is almond taste. Above 75 °c, explosive vapor/air mixtures may form.

Last Update:2024-01-02 23:10:35

100-47-0 - Preparation Method

Open Data Verified Data

The reaction of benzaldehyde with hydroxylamine-o-sulfonic acid produces a salt of hydroxylammonium sulfonate, which is then converted to benzonitrile by reaction with a base.

Last Update:2022-01-01 10:08:20

100-47-0 - Application

Open Data Verified Data

naturally occurring in baked peanuts, hazelnuts, cocoa, and dairy products. For the preparation of daily chemical essence, and improve the stability of the essence. Soap flavor is available up to 2%.

Last Update:2025-08-19 16:24:40

100-47-0 - Safety

Open Data Verified Data

The rat acute oral LD50 was 720-1500mg/kg, the rat percutaneous LD50 value was 1200mg/kg, and the rabbit was 1250mg/kg. A moderate degree of irritation was observed after 1 day of application to rabbit skin under closed conditions; No irritation was found in a closed skin contact test in humans with a 2% concentration of Vaseline preparation.

Last Update:2022-01-01 10:08:21

100-47-0 - Reference Information

relative polarity 0.333
LogP1.5 at 20℃
NIST chemical information Information provided by: webbook.nist.gov (external link)
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
Uses Benzonitrile is usually used as a precursor for the synthesis of a variety of aromatic compounds and forms a stable coordination complex with transition metals.
used as pesticides, dye intermediates and solvent antioxidants, etc.
mainly used as intermediates for advanced coatings such as benzylmelamine, as well as intermediates for synthetic pesticides, aliphatic amines, benzoic acids, and as solvents for nitrile rubber, resins, polymers and coatings. The series of intermediates derived from benzylnitrile are mainly: benzylamine, benzamide, thiobenzamide, haloimide, imine ester, thioimine ester, amidoxime, hydrazine and so on.
Mainly used for dyeing cotton and vitamin/cotton blended fabrics
intermediates and solvents.
production method 1. benzoic acid method benzoic acid is obtained by ammoniation. The catalyst is alumina, and the reaction temperature is 250~350 ℃. 2. Ammonia oxidation method is obtained by oxidizing toluene with air in the presence of ammonia. Toluene is oxidized by vanadium-chromium catalyst at 350 ℃ and then rectified to obtain the finished product. Raw material consumption quota: toluene 2000kg/t, ammonia 1200kg/t. Other methods include diazotization of aniline hydrochloride and nitrous acid, and then react with cuprous cyanide; benzamide reacts with dichlorosulfoxide to prepare benzonitrile. In the above method, cuprous cyanide can be obtained by the action of copper sulfate and potassium cyanide. For example, 60g of copper sulfate, 50g of potassium cyanide and 90ml of water are prepared into cuprous cyanide solution, preheated to 60-70 ℃, 18.6g of aniline, 50ml of hydrochloric acid, 16g of sodium nitrite and 125ml of diazonium salt cold solution are added in batches under intense stirring, the reaction temperature does not exceed 60-70 ℃, and 16g of benzonitrile is separated to be obtained with a yield of 77%.
category toxic substances
toxicity classification poisoning
acute toxicity oral administration-rat LDL0: 720 mg/kg; Oral administration-mouse LD50: 971 mg/kg
stimulation data skin-rabbit 500 mg/24 hours moderate
flammability hazard characteristics more flammable; high heat emits toxic nitrogen oxides and cyanide gas
storage and transportation characteristics warehouse ventilation and low temperature drying; Store separately from oxidants, acids and food additives
fire extinguishing agent dry powder, foam, carbon dioxide, sand; disable acid-base fire extinguishing agent
occupational standard STEL 1 mg/m3
spontaneous combustion temperature 550°C
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
immediate life-threatening and health concentration 14 ppm (66 mg/m3)
Last Update:2024-04-09 19:55:45
100-47-0
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Mobile: 18916960931
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View History
100-47-0
13734-40-2
1074-99-3
60658-41-5
198545-76-5
c.i. 21095
FEMA 2870
AFB STAIN
PRIMAQUINEPHOSPHATE,USP
3-DIETHYLAMINO-1-PROPYLAMINE FOR SYNTHES
Raw Materials for 100-47-0
Toluene
Ammonia
Downstream Products for 100-47-0
3-Nitrobenzonitrile
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