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Naphthaleneacetic Acid

  • CAS:86-87-3
  • MF:C12H10O2
  • Purity:99%
  • Molecular Weight:186.21
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Product Details

  • CAS: 86-87-3
  • MF: C12H10O2
  • Appearance: white to off white crystals
  • Quality Manufacturer Supply High Purity 99% Naphthaleneacetic Acid 86-87-3 with Reasonable Price

    • Molecular Formula:C12H10O2
    • Molecular Weight:186.21
    • Appearance/Colour:white to off white crystals 
    • Vapor Pressure:3.13E-06mmHg at 25°C 
    • Melting Point:126-133.5 oC 
    • Refractive Index:1.6010 (estimate) 
    • Boiling Point:373.207 °C at 760 mmHg 
    • PKA:4.30±0.30(Predicted) 
    • Flash Point:270.1 °C 
    • PSA:37.30000 
    • Density:1.263 g/cm3 
    • LogP:2.46690 

    1-Naphthalene acetic acid(Cas 86-87-3) Usage

    Biochem/physiol Actions

    1-Naphthaleneacetic acid is one of the synthetic auxins, used in plant propagation. It can induce the formation of lateral and adventitious roots.

    Hazard

    Skin irritant.

    Trade name

    AGRONAA?; ALCO? NAA; ALPHASPRA ?; AMCOTONE? APPL-SET?; CELMONE?; DESTRUXOL?; DIP’N GROW?; FRUITONE?; GOLDENGRO?; HORMEX?; KLINGTITE?; LIQUISTIK ?; NAA 800?; NAFUSAKU?; NIAGARASTIK ?; NU-TONE?; PARMONE?; PHYMONE?; PIMACOL-SOL?; PLANOFIX?; PLUCKER?; PRIMACOL?; RHIZOPON B ROOTING POWDER; ROOTONE? (component, with Indole-3-butyric acid and 1-Naphthaleneacetamide); STAFAST?; STIK?; STOPDROP ?; TEKKAM?; TIPOFF?; TRANSPLANTONE? (component, with 1-Naphthaleneacetamide); TREHOLD ?; VARDHAK?

    Safety Profile

    Poison by intraperitoneal route. Moderately toxic by ingestion. Mutation data reported. A skin, mucous membrane, and severe eye irritant. Can cause depression. A pesticide, When heated to decomposition it emits acrid smoke and irritating fumes.

    Potential Exposure

    1-Naphthaleneacetic acid is a carboxylic acid plant growth regulator used for thinning fruit sets in apples, pears, olives, and some citrus. Induces root formation on cuttings and transplants. Inhibits fruit drops. Not currently registered in EU countries (may be pending).

    Shipping

    UN1759 Corrosive solids, n.o.s., Hazard Class: 8; Labels: 8-Corrosive material, Technical Name Required.

    Purification Methods

    Crystallise the acid from EtOH or water. [Beilstein 9 H 666, 9 IV 2424.]

    Incompatibilities

    Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides, chlorates nitrates, ammonia, aliphatic amines, alkanolamines, isocyanates, alkylene oxides, epichlorohydrin. Compounds of the carboxyl group react with all bases, both inorganic and organic (i.e., amines) releasing substantial heat, water and a salt that may be harmful. Incompatible with arsenic compounds (releases hydrogen cyanide gas), diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides (releasing heat, toxic, and possibly flammable gases), thiosulfates and dithionites (releasing hydrogen sulfate and oxides of sulfur).

    Waste Disposal

    Incineration. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers.

    uses

    1-Naphthaleneacetic acid is widely employed in agriculture as a synthetic plant hormone in the auxin family or a plant growth regulator, which can find applications in tissue culture.1-Naphthaleneacetic acid (NAA) is a synthetic phytohormone auxin that is added to cell culture media such as Murashige & Skoog media and Chu′s N6 media.1-Naphthaleneacetic acid has been used:to modify MS media for the initiation of callusas a supplement in solid K3 medium for the selection of transformantsin the preparation of culture medium like V-KM medium and Cg medium

    Definition

    1-Naphthaleneacetic acid is a naphthylacetic acid substituted by a carboxymethyl group at position 1.

    General Description

    1-Naphthaleneacetic acid is widely employed in agriculture as a synthetic plant hormone in the auxin family or a plant growth regulator, which can find applications in tissue culture.

    Agricultural Uses

    Plant growth regulator: An agent for thinning fruit sets in apples, pears, olives and some citrus. Induces root formation on cuttings and transplants. Inhibits fruit drops. Not currently registered in EU countries (pending). Registered for use in the U.S. and Canada.

    InChI:InChI=1/C12H10O2/c13-12(14)8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7H,8H2,(H,13,14)/p-1

    86-87-3 Relevant articles

    -

    Wolthuis,E.,Vander Jagt,D.L.

    , p. 963 - 964 (1964)

    -

    Decatungstate anion as an efficient photocatalytic species for the transformation of the pesticide 2-(1-naphthyl)acetamide in aqueous solution

    Sousa Da Silva, Eliana,Sarakha, Mohamed,Burrows, Hugh D.,Wong-Wah-Chung, Pascal

    , p. 61 - 73 (2017)

    The degradation and mineralization of th...

    -

    Ogata,Ishiguro

    , p. 4302 (1950)

    -

    -

    Southwick et al.

    , p. 754 (1954)

    -

    Radical chemistry of glucosamine naphthalene acetic acid and naphthalene acetic acid: A pulse radiolysis study

    Shibin, Naduvilpurakkal B.,Sreekanth, Radhakrishnan,Aravind, Usha K.,Afsal Mohammed, Kadavilpparampu M.,Chandrashekhar, Narayana V.,Joseph, Jayan,Sarkar, Sisir K.,Naik, Devidas B.,Aravindakumar, Charuvila T.

    , p. 478 - 483 (2014)

    Free radical-induced oxidation reactions...

    Preparation method of naphthalene ring C marked α .

    -

    , (2021/10/05)

    The invention discloses C labeled α - na...

    Desulfonylative Electrocarboxylation with Carbon Dioxide

    Zhong, Jun-Song,Yang, Zi-Xin,Ding, Cheng-Lin,Huang, Ya-Feng,Zhao, Yi,Yan, Hong,Ye, Ke-Yin

    supporting information, p. 16162 - 16170 (2021/09/02)

    Electrocarboxylation of organic halides ...

    Hydrolysis of amides to carboxylic acids catalyzed by Nb2O5

    Siddiki,Rashed, Md. Nurnobi,Touchy, Abeda Sultana,Jamil, Md. A. R.,Jing, Yuan,Toyao, Takashi,Maeno, Zen,Shimizu, Ken-Ichi

    , p. 1949 - 1960 (2021/03/26)

    Hydrolysis of amides to carboxylic acids...

    BF3·OEt2-promoted tandem Meinwald rearrangement and nucleophilic substitution of oxiranecarbonitriles

    Xu, Chuangchuang,Xu, Jiaxi

    , p. 127 - 134 (2019/12/26)

    Tandem Meinwald rearrangement and nucleo...

    86-87-3 Process route

    diazoacetic acid ethyl ester
    623-73-4

    diazoacetic acid ethyl ester

    naphthalene
    91-20-3,71998-51-1,72931-45-4

    naphthalene

    naphth-1-yl acetic acid
    86-87-3

    naphth-1-yl acetic acid

    1a,7b-dihydro-1H-cyclopropa[a]naphthalene-1-exo-carboxylic acid
    16650-36-5,35729-17-0,76376-66-4,59019-93-1

    1a,7b-dihydro-1H-cyclopropa[a]naphthalene-1-exo-carboxylic acid

    2-naphthylacetic acid
    581-96-4

    2-naphthylacetic acid

    Conditions
    Conditions Yield
    tetrakis(trifluoroacetato)rhodium(II); In dichloromethane; for 2.25h;
    3-methoxy-2-[1]naphthyl-acrylic acid ethyl ester

    3-methoxy-2-[1]naphthyl-acrylic acid ethyl ester

    formic acid
    64-18-6

    formic acid

    naphth-1-yl acetic acid
    86-87-3

    naphth-1-yl acetic acid

    Conditions
    Conditions Yield

    86-87-3 Upstream products

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      naphthalen-1-ylacetonitrile

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      ethyl 2-(1-naphthyl)acetate

    • 60-29-7
      60-29-7

      diethyl ether

    • 15719-64-9
      15719-64-9

      methylammonium carbonate

    86-87-3 Downstream products

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      3-naphthalen-1-ylmethylene-3H-isobenzofuran-1-one

    • 835-31-4
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      naphazoline

    • 5121-00-6
      5121-00-6

      naphthalen-1-yl-acetyl chloride

    Relevant Products

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