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Diphenylacetonitrile

CAS No.
86-29-3
Chemical Name:
Diphenylacetonitrile
Synonyms
DIPAN;DPAN;dibenzylcyanide;-Cyanodiphenylmethane;Acetonitrile, diphenyl-;alpha-Cyanodiphenylmethane;Benzeneacetonitrile, α-phenyl-;alpha-phenylbenzeneacetonitrile;usafkf-13;USAF kf-13
CBNumber:
CB2782757
Molecular Formula:
C14H11N
Molecular Weight:
193.25
MDL Number:
MFCD00001862
MOL File:
86-29-3.mol
MSDS File:
SDS
Last updated:2024-09-05 22:20:32

Diphenylacetonitrile Properties

Melting point 71-73 °C (lit.)
Boiling point 181 °C/12 mmHg (lit.)
Density 1.1061 (rough estimate)
vapor pressure 21.3 hPa (190 °C)
refractive index 1.5850 (estimate)
Flash point 120 °C
storage temp. Store below +30°C.
solubility INSOLUBLE
form Crystalline Powder
color White to creamy or faint yellow
Water Solubility INSOLUBLE
Merck 14,3316
BRN 1911160
Exposure limits NIOSH: IDLH 25 mg/m3
InChIKey NEBPTMCRLHKPOB-UHFFFAOYSA-N
LogP 2.795-3.197 at 25℃
CAS DataBase Reference 86-29-3(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII QK4W106TKU
NIST Chemistry Reference Benzeneacetonitrile, «alpha»-phenyl-(86-29-3)
EPA Substance Registry System Diphenylacetonitrile (86-29-3)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H303-H335-H315-H319
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
WGK Germany  2
RTECS  AL9800000
TSCA  Yes
HS Code  29269095
Toxicity LD50 orally in Rabbit: 3500 mg/kg
NFPA 704
0
1 0

Diphenylacetonitrile price More Price(28)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 8.03259 Diphenylacetonitrile for synthesis 86-29-3 100g $11.5 2024-03-01 Buy
Sigma-Aldrich 112127 Diphenylacetonitrile 98% 86-29-3 500g $24.8 2024-03-01 Buy
Sigma-Aldrich 112127 Diphenylacetonitrile 98% 86-29-3 100g $44.6 2024-03-01 Buy
TCI Chemical D0261 Diphenylacetonitrile >99.0%(GC) 86-29-3 25g $23 2024-03-01 Buy
TCI Chemical D0261 Diphenylacetonitrile >99.0%(GC) 86-29-3 500g $139 2024-03-01 Buy
Product number Packaging Price Buy
8.03259 100g $11.5 Buy
112127 500g $24.8 Buy
112127 100g $44.6 Buy
D0261 25g $23 Buy
D0261 500g $139 Buy

Diphenylacetonitrile Chemical Properties,Uses,Production

Chemical Properties

Diphenylacetonitrile is a white to creamy or faint yellow crystalline powder, Soluble in ethanol, ether. It is obtained by bromination and condensation of phenylacetonitrile. Diphenylacetonitrile is mainly used as an intermediate to manufacture API which deals in treatment of respiratory stimulant. It is used to manufacture APIs like stomach amine, Aminepentamide Sulphate, Diphenoxylate, Diphenylacetaldehyde, Doxapram, Loperamide, Methadone.

Uses

Mathadone (M225865) impurity. Used in synthesis of methadone, antispasmodics and other pharmaceuticals.
Diphenylacetonitrile is used to synthesize isocyanate, which is further prepared into UV paint, PU paint, transparent elastomer and adhesive, etc. In addition, it is also used in polyamide and epoxy resin industries.

Preparation

In a 100 mL, nitrogen-flushed pear flask was added indium(III) bromide (2.0 mmol, 10 mol %) in CH2Cl2 (40 mL) to give a white suspension. To this at room temperature was added trimethylsilyl cyanide (40 mmol, 2.0 equiv.), followed by dropwise addition of alcohol (20 mmol, 1.0 equiv.) to give a moderate exothermic reaction. The mixture slowly turned clear, and TLC showed mostly the desire product. Saturated NaHCO3 was added and the mixture was concentrated in vacuo to remove the volatiles. The residue was partitioned between saturated NaHCO3 and ethyl acetate, and the aqueous layer was extracted one more time with ethyl acetate. Combined organic layers were dried over MgSO4, filtered and concentrated. The crude product was purified by flash column chromatography on silica gel (5% ethyl acetate/hexanes) to give the desired Diphenylacetonitrile.

Preparation

Diphenylacetonitrile can be prepared in good yield by the dehydration of the amide of diphenyl acetic acid with phosphorous oxychloride. Diphenylacetonitrile undergoes anhydrous condensation with ethyl-4-bromo-butyrate. This is followed by its hydrolysis in alkaline medium that is used in the quantitative determination of 3-cyano-3,3-diphenylpropionic acid.

Reactions

Methadone is synthesised by alkylation of diphenylacetonitrile using 2-dimethylaminopropylchloride in the presence of sodamide.
Dextromoramide is synthesised by alkylation of diphenylacetonitrile using 1-morpholinyl-2- chloropropane in the presence of sodamide.
Diphenylacetonitrile in the presence of sodium amide is alkylated with 1-ethyl-3-chlorpyrrolidine, giving (1-ethyl-3-pyrrolidinyl) diphenylacetonitrile.
Isopropamide, is synthesized by alkylating diphenylacetonitrile with di-isopropylaminoethylchloride in the presence of sodium amide, and the subsequent hydrolysis of the nitrile group of the resulting compound to an amide group.

Synthesis Reference(s)

The Journal of Organic Chemistry, 35, p. 3253, 1970 DOI: 10.1021/jo00835a016

General Description

Diphenylacetonitrile can be prepared in good yield by the dehydration of the amide of diphenyl acetic acid with phosphorous oxychloride.

Safety Profile

Poison by ingestion, intraperitoneal, and intravenous routes. Moderately toxic by subcutaneous route. Questionable carcinogen with experimental carcinogenic and tumorigenic data. When heated to decomposition it emits toxic fumes of NOx, and CN-. See also NITRILES.

Synthesis

Add the 250mL ethyl acetate in 500mL glass there-necked flask, open and stir, add the 150g phenylcarbinol, add sodium methylate 80g, 70 ℃ of stirring reactions 2 hours are down to room temperature, add benzyl cyanide 120ml.Be heated to 110 ℃, distillation reaction 10h.Reaction naturally cools to room temperature after finishing, and adds the extraction of 200ml ethyl acetate and 200ml water, tells lower aqueous layer.The upper strata ethyl acetate layer adds water, and washing once adds anhydrous sodium sulfate drying.Concentrating under reduced pressure is removed ethyl acetate.Then in oily matter, add a small amount of dehydrated alcohol crystallisation by cooling, the crystallized product oven dry.Yield 90%, purity 99.0% (GC).

Purification Methods

Crystallise the nitrile from EtOH or pet ether (b 90-100o). [Beilstein 9 H 674, 9 IV 2505.]

5798-79-8
71-43-2
86-29-3
Synthesis of Diphenylacetonitrile from Bromobenzyl cyanide and Benzene
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Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Diphenylacetonitrile pictures 2024-11-28 Diphenylacetonitrile
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US $5000.00-3000.00 / ton 1ton 99% 5000 HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
Diphenylacetonitrile pictures 2024-11-28 Diphenylacetonitrile
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US $6.00 / kg 1kg 99% 2000KG/Month HebeiShuoshengImportandExportco.,Ltd
Diphenylacetonitrile pictures 2024-11-28 Diphenylacetonitrile
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US $1.00 / g 1g 99% 1000kg Dorne Chemical Technology co. LTD
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