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Trihexylboron is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1188-92-7 Structure
  • Basic information

    1. Product Name: Trihexylboron
    2. Synonyms: Trihexylboron;Tri-n-hexylborane
    3. CAS NO:1188-92-7
    4. Molecular Formula: C18H39B
    5. Molecular Weight: 266.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1188-92-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 339.2°C at 760 mmHg
    3. Flash Point: 158.9°C
    4. Appearance: /
    5. Density: 0.766g/cm3
    6. Vapor Pressure: 0.000184mmHg at 25°C
    7. Refractive Index: 1.424
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Trihexylboron(CAS DataBase Reference)
    11. NIST Chemistry Reference: Trihexylboron(1188-92-7)
    12. EPA Substance Registry System: Trihexylboron(1188-92-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1188-92-7(Hazardous Substances Data)

1188-92-7 Usage

Purification Methods

Treat the borane with hex-1-ene and 10% anhydrous Et2O for 6hours at gentle reflux under N2, then distil it in a vacuum through an 18inch glass helices-packed column under N2 taking the fraction b 130o/2.1mm to 137o/1.5mm. The distillate may still contain some di-n-hexylborane [Brown & Subba Rao J Am Chem Soc 81 6423 1959, Mirviss J Am Chem Soc 83 3051 1961]. [Beilstein 4 IV 4362.]

Check Digit Verification of cas no

The CAS Registry Mumber 1188-92-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,8 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1188-92:
(6*1)+(5*1)+(4*8)+(3*8)+(2*9)+(1*2)=87
87 % 10 = 7
So 1188-92-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H39B/c1-4-7-10-13-16-19(17-14-11-8-5-2)18-15-12-9-6-3/h4-18H2,1-3H3

1188-92-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name trihexylborane

1.2 Other means of identification

Product number -
Other names Trihexyl-boran

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1188-92-7 SDS

1188-92-7Relevant articles and documents

Organoboranes. 49. An examination of convenient procedures for the generation of borane and monoalkyl- and dialkylboranes from lithium borohydride and monoalkyl- and dialkylborohydrides

Cole, Thomas E.,Bakshi, Raman K.,Srebnik, Morris,Singaram, Bakthan,Brown, Herbert C.

, p. 2303 - 2307 (2008/10/08)

The simple preparation of monoalkyl- and dialkylboranes previously developed by the addition of methyl iodide to lithium monoalkyl- and dialkylborohydrides in tetrahydrofuran solution has been expanded to alternative procedures involving other solvents, such as diethyl ether (EE) and n-pentane, and other reagents, such as phenol, acetic acid, methanesulfonic acid, ethereal hydrogen chloride, trimethylsilyl chloride, and trimethylsilyl methanesulfonate. The practicality of generating monoalkyl- and dialkylboranes from the corresponding borohydrides has been demonstrated in representative solvents utilizing appropriate reagents. The reaction of lithium borohydride with the above reagents was also studied. The reaction of lithium borohydride with 1 equiv of acetic acid produces a mixture of lithium tetraacetoxyborohydride and unreacted lithium borohydride instead of the expected lithium monoacetoxyborohydride. Because of discrepancies with the reported results for sodium borohydride, the study was extended to this reagent.

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