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Detail of "99-06-9"

  • CAS Number:
  • 99-06-9
  • Name:

  • 3-Hydroxybenzoic acid

  • Molecular Structure:
  • Formula:
  • C7H6O3
  • Molecular Weight:
  • 138.12 .
  • Synonyms:
  • Benzoicacid, m-hydroxy- (8CI);3-Carboxyphenol;
  • EINECS:
  • 202-726-5
  • Density:
  • 1.375 g/cm3
  • Melting Point:
  • 201 °C
  • Boiling Point:
  • 346.1 °C at 760 mmHg
  • Flash Point:
  • 177.3 °C
  • Solubility:
  • slightly soluble in water
  • Appearance:
  • white to light yellow crystal powder
  • Hazard Symbols:
  • HarmfulXn,IrritantXi
  • Risk Codes:
  • 22-36/37/38
  • Safety:
  • 26-36/37/39 Details
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CAS No.99-06-9 3-Hydroxybenzoic acid

Assay:99.5%  Appearance:powder  Package:25kg/Cardboa...Storage:1-10MT

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CAS No.99-06-9 3-Hydroxybenzoic acid

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CAS No.99-06-9 3-Hydroxybenzoic acid

Product name:m-hydroxybenzoic acid

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CAS No.99-06-9 3-Hydroxybenzoic acid

Assay:98%

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CAS No.99-06-9 3-Hydroxybenzoic acid

3-HYDROXYBENZOIC ACID---We supply this product in very competitive price.

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CAS No.99-06-9 3-Hydroxybenzoic acid

3-HYDROXY BENZOIC ACID

Supplier:tianjin xintaimei chemical co, ltd. [ China (Mainland)]

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CAS No.99-06-9 3-Hydroxybenzoic acid

Assay:99%  Appearance:colorless cr...  Package:25kg/fiber d...

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CAS No.99-06-9 3-Hydroxybenzoic acid

Assay:99% Min  Package:25Kg/Bag

Meta Hydroxy Benzoic Acid CAS: 99-06-9 packed in

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CAS No.99-06-9 3-Hydroxybenzoic acid

M-Hydroxybenzoic acid purposes : for fungicides, preservatives, plasticizers and pharmaceutical intermediates. Duality is also used synthetic dyes.

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CAS No.99-06-9 3-Hydroxybenzoic acid

Assay:99%

Product name:m-Hydroxybenzoic Acid Molecular Formula C7H6O3 Molecular Weight 138.12 Slightly soluble in water, slightly soluble in benzene, soluble in ethanol Use: As an important organic synthetic intermediate,M-hydroxybenzoic acid is primarily used in synthetic pesti

Supplier:Water Chemical Co.,LTD [ China (Mainland)]

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CAS No.99-06-9 3-Hydroxybenzoic acid

Boc Sciences is the world's leading provider for special chemicals. We offer qualified products for 99-06-9( 3-Hydroxybenzoic acid ),please inquire us for 99-06-9( 3-Hydroxybenzoic acid ).

Supplier:BOC Sciences [ United States]

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CAS No.99-06-9 3-Hydroxybenzoic acid

Purity, % ,min ,99.0 ,HPLC Loss on drying,% max ,0.5 Residuess on ignition : % , max ,0.3 Melting point ,202.5-203.8 °C

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Assay:99%

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CAS No.99-06-9 3-Hydroxybenzoic acid

3-HYDROXYL BENZOIC ACID

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3-Hydroxy Benzoic Acid

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CAS No.99-06-9 3-Hydroxybenzoic acid

5-Hydroxybenzoic acid

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CAS No.99-06-9 3-Hydroxybenzoic acid

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Reference

Ripening of sugarcane by use of certain monosubstituted benzoic acids
Ripening of sugarcane by use of certain monosubstituted benzoic acids. Nickell, Louis G. (Hawaiian Sugar Planters' Assoc., USA). U.S. US 3994712 30 Nov 1976, 4 pp. (English). (United States of America). CODEN: USXXAM. CLASS: IC: A01N009-24. NCL: 071105000. APPLICATION: US 75-584341 6 Jun 1975. DOCUMENT TYPE: Patent CA Section: 5 (Agrochemicals) The sucrose [57-50-1] yield of sugarcaneis increased by treating the cane a few weeks prior to harvesting with the title compds. Thus, 38 mg 3-hydroxybenzoic acid [99-06-9]/stalk applied 4 weeks before harvest gave a pol % cane of 12. 118-91-2 and 57-50-1 which are cas registry numbers of chemicals are mentioned.39 as compared to 5.59 for the cane treated with Trysben (std.) and 7.03 for the control (untreated). .
Bacterial decarboxylation of o-phthalic acids
Bacterial decarboxylation of o-phthalic acids. Taylor, Barrie F.; Ribbons, Douglas W. (Rosenstiel Sch. Mar. Atmos. Sci., Univ. Miami, Miami, FL 33149-1098, USA). Appl. Environ. Microbiol., 46(6), 1276-81 (English) 1983. CODEN: AEMIDF. ISSN: 0099-2240. DOCUMENT TYPE: Journal CA Section: 61 (Water) The decarboxylation of phthalic acids was studied with Bacillus species strain FO, a marine mixed culture ON-7, and Pseudomonas testosteroni. The mixed culture ON-7, when grown anaerobically on phthalate but incubated aerobically with chloramphenicol, quant. converted phthalic acid [88-99-3] to benzoic acid. [65-85-0]. Substituted phthalic acids were also decarboxylated: 4,5-dihydroxyphthalic acid [63958-66-7] to protocatechuic acid [99-50-3]; 4-hydroxyphthalic acid [610-35-5] and 4-chlorophthalic acid [89-20-3] to 3-hydroxybenzoic acid [99-06-9] and 3-chlorobenzoic acid [535-80-8], resp.; and 3-fluorophthalic acid [1583-67-1] to 2- [445-29-4] and 3-fluorobenzoic acid [455-38-9]. Bacillus Species strain FO gave similar results, except that 4,5-dihydroxyphthalic acid was not metabolized, and both 3- and 4-hydroxybenzoic acid [99-96-7] were produced from 4-hydroxyphthalic acid. P. testosteroni Decarboxylated 4-hydroxyphthalate (to 3-hydroxybenzoate) and 4,5-dihydroxyphthalate, but not phthalic acid and halogenated phthalates. Thus, P. testosteroni and the mixed culture ON-7 possessed 4,5-dihydroxyphthalic acid decarboxylase [37290-48-5], previously described in P. testosteroni, that metabolized 4,5-dihydroxyphthalic acid and specifically decarboxylated 4-hydroxyphthalic acid to 3-hydroxybenzoic acid. The mixed culture ON-7 and Bacillus species strain FO also possessed a novel decarboxylase that metabolized phthalic acid and halogenated phthalates, but not 4,5-dihydroxyphthalate, and randomly decarboxylated 4-hydroxyphthalic acid. It is suggested that the decarboxylation of phthalic acid involves an initial redn. to 1,2-dihydrophthalic acid, followed by oxidative decarboxylation to benzoic acid.
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