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Merck
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Key Documents

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Safety Information

T83607

Sigma-Aldrich

Bromotriphenylmethane

98%

Synonym(s):

Triphenylbromomethane, Trityl bromide

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25 G
CN¥409.09
100 G
CN¥1,554.53

CN¥409.09

Estimated to ship onJune 20, 2025Details

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25 G
CN¥409.09
100 G
CN¥1,554.53

About This Item

Linear Formula:
(C6H5)3CBr
CAS Number:
596-43-0
Molecular Weight:
323.23
Beilstein:
1878494
EC Number:
209-884-4
MDL number:
MFCD00000120
UNSPSC Code:
12352100
PubChem Substance ID:
24900521
NACRES:
NA.22

CN¥409.09

Estimated to ship onJune 20, 2025Details

Request a Bulk Order

Assay

98%

bp

230 °C/15 mmHg (lit.)

mp

152-154 °C (lit.)

storage temp.

2-8°C

SMILES string

BrC(c1ccccc1)(c2ccccc2)c3ccccc3

InChI

1S/C19H15Br/c20-19(16-10-4-1-5-11-16,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H

InChI key

NZHXEWZGTQSYJM-UHFFFAOYSA-N

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Show Differences

1 of 4

This Item
360074243965178012
Bromotriphenylmethane 98%

T83607

Bromotriphenylmethane

Magnesium bromide 98%

360074

Magnesium bromide

Phenylselenyl bromide 98%

243965

Phenylselenyl bromide

(1,2-Dibromoethyl)benzene ≥98%

178012

(1,2-Dibromoethyl)benzene

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

storage temp.

2-8°C

storage temp.

-

storage temp.

-

storage temp.

-

mp

152-154 °C (lit.)

mp

711 °C (lit.)

mp

58-62 °C (lit.)

mp

70-74 °C (lit.)

bp

230 °C/15 mmHg (lit.)

bp

-

bp

107-108 °C/15 mmHg (lit.)

bp

139-141 °C/15 mmHg (lit.)

Application

Reagent for the preparation of trityl esters.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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    Lot/Batch Number
    SDBB3333
    STBK5831
    STBK2891
    STBK2272
    STBH3141

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    Siddabasave Gowda B Gowda et al.
    Lipids, 55(4), 395-401 (2020-05-15)
    An efficient three-step strategy for the convenient synthesis of Sn-glycero-3-phosphoethanolamine (GroPEtn) from a commercially available 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine (DPPE) is reported. Direct hydrolysis of DPPE produces a complex inseparable mixture, hence a protection and deprotection strategy is employed to prepare GroPEtn. The
    Yusuke Yamamoto et al.
    Analytical and bioanalytical chemistry, 413(1), 245-254 (2020-10-23)
    Lysophosphatidylethanolamines (LysoPEs) are the partial hydrolysis products of phosphatidylethanolamine. Despite the unique in vitro bioactivities of LysoPEs, there are limited reports on the pathophysiological role of LysoPEs in the serum, due to the lack of sensitive analytical methods for determination
    Krzysztof Matyjaszewski et al.
    Molecules (Basel, Switzerland), 26(2) (2021-01-14)
    N-alkyl phosphoranimines were synthesized via the Staudinger reaction of four different alkyl azides with tris(2,2,2-trifluoroethyl) phosphite. N-adamantyl, N-benzyl, N-t-butyl, and N-trityl phosphoranimines were thoroughly characterized and evaluated as chain-capping compounds in the anionic polymerization of P-tris(2,2,2-trifluoroethoxy)-N-trimethylsilyl phosphoranimine monomer. All four
    Cansu Aydogan et al.
    Macromolecular rapid communications, 40(14), e1900109-e1900109 (2019-05-16)
    A straightforward transformation protocol combining two distinct living polymerization methods for the controlled synthesis of block copolymers is described. In the first step, bromo-terminated poly(methyl methacrylate) is prepared by atom transfer radical polymerization (ATRP). Then, a bromide end group is
    Salvatore Debonis et al.
    Journal of medicinal chemistry, 51(5), 1115-1125 (2008-02-13)
    The human kinesin Eg5 is a potential drug target for cancer chemotherapy. Eg5 specific inhibitors cause cells to block in mitosis with a characteristic monoastral spindle phenotype. Prolonged metaphase block eventually leads to apoptotic cell death. S-trityl-L-cysteine (STLC) is a

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