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2,3-bis(dibromomethyl)naphthalene, commonly referred to as DBN, is a white to off-white solid chemical compound characterized by a distinct odor and insolubility in water. It is primarily recognized for its role as a flame retardant, which is attributed to its capacity to release bromine radicals upon exposure to heat, thereby inhibiting combustion and slowing the spread of flames.

71383-01-2

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71383-01-2 Usage

Uses

Used in Plastics Industry:
2,3-bis(dibromomethyl)naphthalene is used as a flame retardant in the plastics industry to enhance the fire resistance of various plastic materials, thereby reducing the risk of fire and improving safety standards in products.
Used in Textile Industry:
In the textile industry, 2,3-bis(dibromomethyl)naphthalene serves as a flame retardant, ensuring that fabrics and other textile products possess a higher level of fire resistance, which is crucial for applications in upholstery, carpets, and clothing.
Used in Foam Products:
2,3-bis(dibromomethyl)naphthalene is utilized as a flame retardant in the production of foam products, such as in furniture and insulation materials, to improve their fire safety performance and mitigate the hazards associated with fire incidents.
However, it is important to note that the use of DBN has been a subject of concern due to its potential environmental and health impacts. As a brominated flame retardant, DBN is known to be persistent, bioaccumulative, and potentially toxic, which necessitates careful consideration and ongoing research into safer alternatives or methods to mitigate its risks.

Check Digit Verification of cas no

The CAS Registry Mumber 71383-01-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,3,8 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71383-01:
(7*7)+(6*1)+(5*3)+(4*8)+(3*3)+(2*0)+(1*1)=112
112 % 10 = 2
So 71383-01-2 is a valid CAS Registry Number.

71383-01-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-bis(dibromomethyl)naphthalene

1.2 Other means of identification

Product number -
Other names 2,3-bis-dibromomethyl-naphthalene

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:71383-01-2 SDS

71383-01-2Relevant academic research and scientific papers

Intramolecular Singlet Fission in Oligoacene Heterodimers

Sanders, Samuel N.,Kumarasamy, Elango,Pun, Andrew B.,Steigerwald, Michael L.,Sfeir, Matthew Y.,Campos, Luis M.

, p. 3373 - 3377 (2016)

We investigate singlet fission (SF) in heterodimers comprising a pentacene unit covalently bonded to another acene as we systematically vary the singlet and triplet pair energies. We find that these energies control the SF process, where dimers undergo SF provided that the resulting triplet pair energy is similar or lower in energy than the singlet state. In these systems the singlet energy is determined by the lower-energy chromophore, and the rate of SF is found to be relatively independent of the driving force. However, triplet pair recombination in these heterodimers follows the energy gap law. The ability to tune the energies of these materials provides a key strategy to study and design new SF materials - an important process for third-generation photovoltaics. Organic electronics: A series of oligoacene heterodimers was synthesized to test the energetic requirements for singlet fission - a photophysical process that yields two triplet excitons from a single photon. Thus a possibility is offered to tune this process.

QUANTITATIVE INTRAMOLECULAR FISSION IN OLIGOACENES, MATERIALS, AND METHODS OF USE THEREOF

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Page/Page column 47, (2016/07/05)

The present invention provides soluble, stable singlet fission (SF) compounds, compositions, materials, methods of their use, and methods for their preparation that provide efficient intramolecular singlet fission (iSF) and multiple excitons. The SF compo

Synthesis of Benzo-Fused Tetraphenylenes and Crystal Structure of a 4:1 Clathrate Inclusion Compound of Dibenzotetraphenylene with p-Xylene

Man, Yuet-Ming,Mak, Thomas C. W.,Wong, Henry N. C.

, p. 3214 - 3221 (2007/10/02)

Benzo-fused tetraphenylenes 2-6 were successfully prepared by the combined deployment of the Diels-Alder cycloaddition between some strained cyclooctynes and furans and subsequent low-valent-titanium deoxygenation of the resulting 1,4-endoxides.As expecte

Naphthaquinone anti-psoriatic agents

-

, (2008/06/13)

Psoriasis in mammals is relieved by topically administering substituted naphthaquinones of the formula: STR1 where R1 and R2 are the same or different and are hydrogen, hydroxy, alkoxy or acylamino and R3 is hydrogen, halo

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