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Detail of "3332-29-4"

  • CAS Number:
  • 3332-29-4
  • Name:

  • Hydroxylamine,O-ethyl-, hydrochloride (1:1)

  • Superlist Name:
  • Ethoxyamine hydrochloride
  • Molecular Structure:
  • Formula:
  • C2H7 NO.ClH
  • Molecular Weight:
  • 97.54
  • Deleted CAS:
  • 253880-86-3|188720-08-3
  • Synonyms:
  • Ethoxyamine,hydrochloride (6CI,7CI);Hydroxylamine, O-ethyl-, hydrochloride (8CI,9CI);(Aminooxy)ethane hydrochloride;Ethoxamine hydrochloride;Ethoxyammoniumchloride;N-Ethoxyamine hydrochloride;O-Ethylhydroxylamine hydrochloride;
  • EINECS:
  • 222-060-9
  • Melting Point:
  • 130-133 °C(lit.)
  • Boiling Point:
  • 75.8 °C at 760 mmHg
  • Flash Point:
  • 5.9 °C
  • Appearance:
  • white adhering crystals or crystalline powder
  • Hazard Symbols:
  • IrritantXi
  • Risk Codes:
  • 36/37/38
  • Safety:
  • 26-36 Details
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CAS No.3332-29-4 Ethoxyamine hydrochlorideCompetitive Product

Assay:≥99.0%  Appearance:White or yel...  Package:25kg/barrel,...

Ethoxyamine hydrochloride Chemical Name:Ethoxyamine Hydrochloride, O-Ethoxyamine Hydrochloride CAS No.:3332-29-4 Physical data and specifications: Melting point:130.0-133.0℃ Water content:≤0.5%

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CAS No.3332-29-4 Ethoxyamine hydrochlorideCompetitive Product

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CAS No.3332-29-4 Ethoxyamine hydrochlorideCompetitive Product

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CAS No.3332-29-4 Ethoxyamine hydrochloride

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CAS No.3332-29-4 Ethoxyamine hydrochloride

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

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CAS No.3332-29-4 Ethoxyamine hydrochloride

Name: Ethoxyamine hydrochloride EINECS: 222-060-9 Molecular Formula: C2H7NO?HCl CAS No.: 3332-29-4 Synonyms: O-Ethylhydroxylamine hydrochloride; InChI： InChI=1/C2H7NO.ClH/c1-2-4-3;/h2-3H2,1H3;1H Molecular Weight: 97.54 Density: g/cm3 Boiling Point: 75.8 °C at 760

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CAS No.3332-29-4 Ethoxyamine hydrochloride

product Name Ethoxyamine hydrochloride Synonyms O-Ethylhydroxylamine hydrochloride; ; (aminooxy)ethane hydrochloride (1:1) Molecular Formula C2H8ClNO Molecular Weight 97.544 InChI InChI=1/C2H7NO.ClH/c1-2-4-3;/h2-3H2,1H3;1H CAS Registry Number 3332-29-4 EINECS 222-060-9

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CAS No.3332-29-4 Ethoxyamine hydrochloride

Assay:98%  Appearance:White crysta...

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CAS No.3332-29-4 Ethoxyamine hydrochloride

Ethoxy amine hydrochloride

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CAS No.3332-29-4 Ethoxyamine hydrochloride

Assay:98%

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CAS No.3332-29-4 Ethoxyamine hydrochloride

Ethoxylated Amine hydrochloride---We supply this product in very competitive price.

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CAS No.3332-29-4 Ethoxyamine hydrochloride

  Application:Intermediate...

Chemical Name: O-Ethylhydroxylamine Hydrochloride Abbreviation: EHH Structure: CH3CH2ONH2 HCl Molecular Formula: C2H7NO HCl Molecular Weight: 97.54

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CAS No.3332-29-4 Ethoxyamine hydrochloride

Ethoxyamine Hydrochloride

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ETHOXYAMINE HYDROCHLORIDE

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CAS No.3332-29-4 Ethoxyamine hydrochloride

Molecular Formula：C2H7NO·HCl Molecular Weight：97.55 Appearance：white or yellowish crystal Melting Point：130.0~133.0℃ Moisture：≤0.5% G C : ≥99.0% Solubility：easily soluble in water,soluble in ethanol Usage：mainly uses for producing herbicides, like the tralkoxydim, clethodi

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CAS No.3332-29-4 Ethoxyamine hydrochloride

C2H7 N O . Cl H

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ETHOXYAMINE HYDROCHLORIDE

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Reference

Plant growth regulator
Plant growth regulator. Warner, Richard Burridge; Slater, John Walter (Imperial Chemical Industries PLC; ICI Australia Ltd. , UK). Brit. UK Pat. Appl. GB 2124198 A1 15 Feb 1984, 11 pp. (English). (United Kingdom). CODEN: BAXXDU.Some commonly used reagents like 87820-90-4 and 87820-94-8 are used in this experiment. CLASS: IC: A01N031-08; A01N033-16. ICA: C07C049-203; C07C049-573; C07C131-00. APPLICATION: GB 83-15507 6 Jun 1983. PRIORITY: GB 82-17695 18 Jun 1982. DOCUMENT TYPE: Patent CA Section: 5 (Agrochemical Bioregulators) Section cross-reference(s): 25 5-Phenylcyclohexene 1,3-diones I (R1 = H, Ac or Bz; R2 = alkyl, allyl or propargyl; R3 = alkyl, n = 2 or 3) were prepd. and used as growth regulators. Thus, 2-[1-(ethoxyimino)propyl]-3-hydroxy-5-mesitylcyclohex-2-en-1-one (II) [87820-88-0] was prepd. by condensing mesitylaldehyde [487-68-3] with acetone [67-64-1], and the resulting unsatd. ketone was condensed with di-Et malonate [105-53-3], then subjected to alk. hydrolysis followed by acidification and decarboxylation to give 3-hydroxy-5-mesitylcyclohex-2-en-1-one [87821-74-7], which was reacted with propionic anhydride [123-62-6] in presence of NaOMe to give 3-hydroxy-5-mesityl-2-propionylcyclohex-2-en-1-one [87821-75-8]; this product was treated with ethoxyamine-HCl [3332-29-4] to give II. A spray compn. contg. I, Tween 20, Span 80, and methylcyclohexanone, applied (0.1 or 0.2 kg/ha) to young spring and winter barley and spring wheat, at the 3-4 leaf stage, increased the no. of tillers and decreased the height of the plant. I were also applied to soybean, sugar beet, lettuce, cotton, and tomato. .
Herbicidal compositions
Herbicidal compositions. Graciet, Bernard (Imperial Chemical Industries PLC, UK). Eur. Pat. Appl. EP 128642 A1 19 Dec 1984, 22 pp. DESIGNATED STATES: R: BE, CH, DE, FR, GB, IT, LI, NL, SE. (English). (European Patent Organization). CODEN: EPXXDW. CLASS: IC: A01N047-30. ICI: A01N047-30, A01N041-04, A01N037-10, A01N037-04, A01N035-10. APPLICATION: EP 84-302447 10 Apr 1984. PRIORITY: GB 83-13774 18 May 1983. DOCUMENT TYPE: Patent CA Section: 5 (Agrochemical Bioregulators) Section cross-reference(s): 24, 25 Herbicidal formulations which had no phytotoxic effects on winter barley and winter wheat were prepd. comprising a mixt. of isoproturon [34123-59-6] and a substituted cyclohexenone deriv. I (R1 = H, alkyl, or acyl; R2 and R3 = aliph. radical; n = 2-5). Prepn. of I is described. Thus, 2-[(1-ethoxyimino)propyl]-3-hydroxy-5-mesitylcyclohex-2-en-1-one (II) [3332-29-4] was prepd. by condensing mesitylaldehyde [487-68-3] with acetone [67-64-1] to give 1-(2,4,6-trimethylphenyl)but-1-en-3-one [53389-56-3] which was further condensed with diEt malonate [105-53-3], subjected to alk. hydrolysis, acidification and decarboxylation to give 3-hydroxy-5-mesitylcyclohex-2-en-1-one [87821-74-7]; this was reacted with propionic anhydride [123-62-6] to give 3-hydroxy-5-mesityl-2-propionylcyclohex-2-en-1-one [87821-75-8] which was further reacted with ethoxyamine HCl [3332-29-4] to give II. Mixts. of II + isoproturon (100 + 750 g/ha) caused no damage to barley or wheat and controlled 100% Avena fatua and Alopecurus myosuroides.
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