397237

Acetanilide

zone-refined, purified by sublimation, ≥99.95%

Manufacturer: Sigma Aldrich

CAS Number: 103-84-4

Synonym(S): N-Phenylacetamide

Select a Size

Pack Size SKU Availability Price
1 G 397237-1-G In Stock ₹ 13,910.13
5 G 397237-5-G In Stock ₹ 27,744.48

397237 - 1 G

₹ 13,910.13

In Stock

Quantity

1

Base Price: ₹ 13,910.13

GST (18%): ₹ 2,503.823

Total Price: ₹ 16,413.953

grade

zone-refined

Quality Level

100

vapor density

4.65 (vs air)

vapor pressure

1 mmHg ( 114 °C)

Assay

≥99.95%

form

solid

autoignition temp.

1004 °F

purified by

sublimation

bp

304 °C (lit.)

mp

113-115 °C (lit.)

Other Options

Image Product Name Manufacturer Price Range
11-101-2354
Acetaminophen Related Compound D Pharmaceutical Secondary Standard, MilliporeSigma™ Supelco™
MilliporeSigma Supelco ₹ 28,063.68
11-101-2353
Acetanilide melting point standard Pharmaceutical Secondary Standard, MilliporeSigma™ Supelco™
MilliporeSigma Supelco ₹ 11,773.06
50-183-6909
Sigma Aldrich Fine Chemicals Biosciences Acetanilide 99% | 103-84-4 | MFCD00008674 | 100G
Sigma Aldrich Fine Chemicals Biosciences ₹ 5,587.07
50-183-6906
Sigma Aldrich Fine Chemicals Biosciences Acetanilide | 103-84-4 | MFCD00008674 | 5g
Sigma Aldrich Fine Chemicals Biosciences ₹ 9,569.03
50-503-775
Chem-Impex International, Inc. Acetanilide | 103-84-4 | MFCD00008674 | 1KG
Chem-Impex International, Inc. ₹ 8,730.54
NC0741785
U.S. Pharmacopeia Acetanilide Melting Point Standard, 103-84-4, MFCD00008674, 1 g
U.S. Pharmacopeia ₹ 19,809.71
PHR1086
Acetanilide melting point standard
Supelco ₹ 10,153.85
112933
Acetanilide
Sigma Aldrich ₹ 1,104.15 - ₹ 7,566.68
397229
Acetanilide
Sigma Aldrich ₹ 8,259.48 - ₹ 26,510.43
00401
Acetanilide
Sigma Aldrich ₹ 8,259.48

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Description

  • General description: Acetanilide is an aniline derivative. Crystal structure of acetanillide has been studied by X-ray diffraction. It crystallizes in orthorhombic system having space group of Pbca.[1] Its photolysis has been studied in the presence of β-cyclodextrin (cycloheptaamylose).[2] Aminoacetophenone derivatives are obtained by the Fries rearrangement of acetanilide in the presence zeolites Y and β.[3]
  • Application: Acetanilide may be used in the synthesis of ortho-haloacetanilides via regioselective C-H functionalization/halogenation reaction in the presence of Pd(OAc)2 and Cu(OAc)2 catalyst.[4] It may be used in the preparation of chlorosubstituted acetanilides.[5]

SAFETY INFORMATION

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P264 - P270 - P301 + P312 - P501

Hazard Classifications

Acute Tox. 4 Oral

WGK

WGK 1

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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grade:
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Quality Level:
100

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4.65 (vs air)

vapor pressure:
1 mmHg ( 114 °C)

Assay:
≥99.95%

form:
solid

autoignition temp.:
1004 °F

purified by:
sublimation

bp:
304 °C (lit.)

mp:
113-115 °C (lit.)

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