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Salicylamide

CAS No.
65-45-2
Chemical Name:
Salicylamide
Synonyms
2-HYDROXYBENZAMIDE;Cetamide;Salamide;Benesal;Algamon;Salicylamid;OHB;Acket;Samid;Cidal
CBNumber:
CB4854078
Molecular Formula:
C7H7NO2
Molecular Weight:
137.14
MDL Number:
MFCD00007978
MOL File:
65-45-2.mol
MSDS File:
SDS
Last updated:2024-04-24 17:21:45

Salicylamide Properties

Melting point 140-144 °C(lit.)
Boiling point 270°C
Density 1,175 g/cm3
refractive index 1.5323 (estimate)
Flash point 181°C/14mm
storage temp. Inert atmosphere,Room Temperature
solubility methanol: 0.1 g/mL, clear
pka pKa 8.13(H2O t = 37) (Uncertain)
form Crystalline Powder
color White
Odor Odorless
PH Range 5 (0.2% aq soln)
Water Solubility <0.1 g/100 mL at 20 ºC
Decomposition 270°C
Merck 14,8328
BRN 742439
Stability Stable. Light sensitive. Incompatible with strong bases, strong oxidizing agents.
InChIKey SKZKKFZAGNVIMN-UHFFFAOYSA-N
LogP 1.280
FDA 21 CFR 310.545
CAS DataBase Reference 65-45-2(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII EM8BM710ZC
ATC code N02BA05
NIST Chemistry Reference Benzamide, 2-hydroxy-(65-45-2)
EPA Substance Registry System o-Hydroxybenzamide (65-45-2)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P264-P270-P301+P312-P302+P352-P305+P351+P338
Hazard Codes  Xn
Risk Statements  22-36/37/38-20/21/22
Safety Statements  26-36
RIDADR  3249
WGK Germany  3
RTECS  VN6475000
TSCA  Yes
HazardClass  6.1(b)
PackingGroup  III
HS Code  29214300
Toxicity LD50 orally in mice: 1.4 g/kg (Hart)
NFPA 704
1
2 0

Salicylamide price More Price(27)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 84230 Salicylamide puriss., ≥99.0% (T) 65-45-2 1kg $42.4 2024-03-01 Buy
Sigma-Aldrich 1608000 Salicylamide United States Pharmacopeia (USP) Reference Standard 65-45-2 200mg $381 2024-03-01 Buy
TCI Chemical S0006 Salicylamide >98.0%(T) 65-45-2 25g $16 2024-03-01 Buy
TCI Chemical S0006 Salicylamide >98.0%(T) 65-45-2 500g $56 2024-03-01 Buy
Alfa Aesar A10797 Salicylamide, 98% 65-45-2 250g $29.65 2024-03-01 Buy
Product number Packaging Price Buy
84230 1kg $42.4 Buy
1608000 200mg $381 Buy
S0006 25g $16 Buy
S0006 500g $56 Buy
A10797 250g $29.65 Buy

Salicylamide Chemical Properties,Uses,Production

Description

Salicylamide is less acidic (pKa 8.2) than other salicylic acid derivatives. Although poorly soluble in water, stable solutions can be formed at pH 9 through ionization of the phenolic group. It is absorbed from the GI tract on oral administration and is rapidly metabolized to inactive metabolites by intestinal mucosa, but not by hydrolysis. Activity appears to reside in the intact molecule. Salicylamide is approximately 40 to 55% plasma protein bound, and it competes with other salicylates and acetaminophen for glucuronide conjugation, decreasing the extent of conjugation of these other drugs.

Chemical Properties

white or light pink crystals or powder

Uses

Medicine (analgesic).

Uses

Salicylamide is used in combination with both aspirin and caffeine in the over-the-counter pain remedies. It is used as an analgesic and as an antipyretic.

Uses

salicylamide is an analgesic, fungicide, and anti-inflammatory ingredient used to soothe the skin. Salicylamide is an aromatic amide.

Definition

ChEBI: The simplest member of the class of salicylamides derived from salicylic acid.

General Description

Salicylamide, o-hydroxybenzamide, is a derivative of salicylicacid that is fairly stable to heat, light, and moisture. Itreportedly exerts a moderately quicker and deeper analgesiceffect than aspirin because of quicker CNS penetration. Its metabolismdiffers from aspirin, because it is not metabolized tosalicylic acid but rather excreted exclusively as the ether glucuronideor sulfate. Thus, as a result of lack of contributionfrom salicylic acid, it has a lower analgesic and antipyretic efficacythan that of aspirin. However, it can be used in place ofsalicylates for patients with a demonstrated sensitivity to salicylates.It is also excreted much more rapidly than other salicylates,which accounts for its lower toxicity. It is available inseveral nonprescription products, in combination with acetaminophenand phenyltoloxamine (e.g., Rid-A Pain compound,Cetazone T, Dolorex, Ed-Flex, Lobac) or with aspirin,acetaminophen, and caffeine (e.g., Saleto, BC Powder).

General Description

Odorless white or slightly pink crystals. Bitter taste, leaves a sensation of warmth on the tongue. pH (saturated aqueous solution at 82°F) about 5. Sublimation begins at the melting point.

Air & Water Reactions

Salicylamide darkens on exposure to air. . Insoluble in water.

Reactivity Profile

Salicylamide is an amide. Amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx). Salicylamide may be sensitive to prolonged exposure to light.

Fire Hazard

Flash point data for Salicylamide are not available; however, Salicylamide is probably combustible.

Clinical Use

Whereas salicylamide is reported to be as effective as aspirin as an analgetic/antipyretic and is effective in relieving pain associated with arthritic conditions, it does not appear to possess useful anti-inflammatory activity. Thus, indications for the treatment of arthritic disease states are unwarranted, and its use is restricted to the relief of minor aches and pain at a dosage of 325 to 650 mg three or four times per day. Its effects in humans are not reliable, however, and its use is not widely recommended.

Purification Methods

Crystallise the amide from water or repeatedly from CHCl3 [Nishiya et al. J Am Chem Soc 108 3880 1986]. [Beilstein 10 IV 169.] The anilide [87-17-2] M 213.2, m 135o crystallises from H2O. [Beilstein 12 H 500, 12 I 268, 12 II 256, 12 944.]

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View Lastest Price from Salicylamide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Salicylamide pictures 2024-04-24 Salicylamide
65-45-2
US $15.00 / kg 1kg 99.912% 10ton Ouhuang Engineering Materials (Hubei) Co., Ltd
Salicylamide pictures 2024-04-18 Salicylamide
65-45-2
US $6.00 / KG 1KG More than 99% 2000KG/MONTH Hebei Saisier Technology Co., LTD
Salicylamide pictures 2024-04-12 Salicylamide
65-45-2
US $0.00-0.00 / kg 1kg 99 50000KG/month Shanghai Affida new material science and technology center
  • Salicylamide pictures
  • Salicylamide
    65-45-2
  • US $15.00 / kg
  • 99.912%
  • Ouhuang Engineering Materials (Hubei) Co., Ltd
  • Salicylamide pictures
  • Salicylamide
    65-45-2
  • US $6.00 / KG
  • More than 99%
  • Hebei Saisier Technology Co., LTD
  • Salicylamide pictures
  • Salicylamide
    65-45-2
  • US $0.00-0.00 / kg
  • 99
  • Shanghai Affida new material science and technology center
Salicylamide o-Hydroxybenzamide Salamide Deferasirox Benzamide Impurity Salicylamide puriss., >=99.0% (T) O-HYDROXYBENZAMIDE SALICYLAMIDE 2-Carbamoylphenol 2-hydroxy-benzamid 2-hydroxy-benzoicaciamide LABOTEST-BB LT02090583 Acket Afko-Sal Algiamida Allevin Amid kyseliny salicylove Salamid Saliamid Saliamin Salicilamide Salicim Salicylic Acid amide salicylicacidamide Salipur Salizell Salrin Salymid Samid Serramida sr4326 Urtosal amidkyselinysalicylove Amidosal Amid-Sal Anamid Andasol Benzamide, o-hydroxy- Benzamide,2-hydroxy- Cidal component of Tolagesic Cymidon Dolomide Dropsprin Eggosalil Flarpirina H.P. 34 h.p.34 Isonidrin Liquiprin Morsarinas Novecyl OHB o-hydroxy-benzamid Oramid Panithal Raspberin SALICYLAMIDE, PGE. WITH 10 X 10 MG SALICYLAMIDE, MATRIX SUBSTANCE FOR MALDI -MS SALICYLAMIDE, EXTRA PURE, USP Salicylamide NF, Granular