Pular para o conteúdo
Merck
Todas as fotos(1)

Documentos Principais

Visualizar Toda a Documentação

469785

Sigma-Aldrich

Benzyl glycidyl ether

99%

Sinônimo(s):

(Benzyloxymethyl)oxirane, (±)-O-Benzylglycidol, 1-(Benzyloxy)-2,3-epoxypropane, 2-[(Phenylmethoxy)methyl]oxirane, 2-[[(Benzyloxy)methyl]oxy]oxirane, 3-(Benzyloxy)-1,2-epoxypropane, Glycidyl benzyl ether, [(Phenylmethoxy)methyl]oxirane

Faça loginpara ver os preços organizacionais e de contrato

Selecione um tamanho

5 ML
R$ 410,00
25 ML
R$ 1.405,00

R$ 410,00

Check Cart for Availability
Solicite uma grande encomenda
Todas as fotos(1)

Selecione um tamanho

Alterar visualização
5 ML
R$ 410,00
25 ML
R$ 1.405,00

About This Item

Fórmula empírica (Notação de Hill):
C10H12O2
Número CAS:
2930-05-4
Peso molecular:
164.20
Número CE:
220-899-5
Número MDL:
MFCD00068664
Código UNSPSC:
12352100
ID de substância PubChem:
24870484
NACRES:
NA.22

R$ 410,00

Check Cart for Availability
Solicite uma grande encomenda

Ensaio

99%

índice de refração

n20/D 1.5170 (lit.)

p.e.

70-73 °C/11 mmHg (lit.)

densidade

1.077 g/mL at 25 °C (lit.)

grupo funcional

ether
phenyl

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

C(OCc1ccccc1)C2CO2

InChI

1S/C10H12O2/c1-2-4-9(5-3-1)6-11-7-10-8-12-10/h1-5,10H,6-8H2

chave InChI

QNYBOILAKBSWFG-UHFFFAOYSA-N

Categorias relacionadas

Descrição geral

Benzyl glycidyl ether is a glycidyl derivative. Rac-/(R)-benzyl glycidyl ether participates in the synthesis of atactic and isotactic linear poly(benzyl 1,2-glycerol carbonate)s.[1] Biocatalytic resolution of racemic benzyl glycidyl ether by Talaromyces flavus has been described.[2] Resolution of benzyl glycidyl ether to (S)-benzyl glycidyl ether with 30% ee and (R)-3-benzyloxypropane-1,2-diol with 40% ee by whole Bacillus alcalophilus cells has been reported.[3] It reacts with K-, K+(15-crown-5)2 to afford potassium glycidoxide and bibenzyl.[4]

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Declarações de precaução

P302 + P352 - P305 + P351 + P338

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

235.4 °F - closed cup

Ponto de fulgor (°C)

113 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
MKCV1886
MKCR6411
MKCM2781
MKCG2665
MKBJ5309V

Não está vendo a versão correta?

Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

Pesquise por COA

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Slide 1 of 6

1 of 6

2-Ethylhexyl glycidyl ether 98%

Sigma-Aldrich

251747

2-Ethylhexyl glycidyl ether

Ethyl 2,3-epoxypropionate 90%

Sigma-Aldrich

636185

Ethyl 2,3-epoxypropionate

tert-Butyldimethylsilyl glycidyl ether 98%

Sigma-Aldrich

526134

tert-Butyldimethylsilyl glycidyl ether

2,3-Epoxypropyl phenyl ether for synthesis

Sigma-Aldrich

8.20553

2,3-Epoxypropyl phenyl ether

Allyl glycidyl ether ≥99%

Sigma-Aldrich

A32608

Allyl glycidyl ether

1,2-Epoxy-9-decene 96%

Sigma-Aldrich

410829

1,2-Epoxy-9-decene

Selective cleavage of the linear ether bond in benzyl glycidyl ether and triphenylmethyl glycidyl ether by potassium alkalide as two-electron-transfer reagent.
Grobelny Z, et al.
Journal of Organometallic Chemistry, 660(1), 6-13 (2002)
Chun Wei et al.
Biotechnology letters, 34(8), 1499-1503 (2012-04-25)
Talaromyces flavus containing a constitutive epoxide hydrolase (EH) resolved racemic benzyl glycidyl ether and nine derivatives into their (R)-enantiomers. After optimization of the fermentation conditions, the specific EH activity and biomass concentration were improved from 13.5 U/g DCW and 14.8
Qingjie Zhang et al.
Nanomaterials (Basel, Switzerland), 8(9) (2018-09-12)
A surface-sizing technique was offered to take full advantage of multi-walled carbon nanotubes (MWCNTs) and epoxy resins. Two surface-sizing treated MWCNTs were obtained through a ball-milling treatment of amino-functionalized MWCNTs (MWCNT-NH₂) with n-butyl glycidylether (BuGE) and benzyl glycidylether (BeGE). These
Youlin Pan et al.
Chemistry, an Asian journal, 12(11), 1198-1203 (2017-03-21)
Cyclic azasilanes have been synthesized for the purpose of developing coupling agents appropriate for a variety of nanotechnologies including surface modification of nanoparticles, nanocrystals, mesoporous materials and substrates. N-Methyl-aza-2,2,4-trimethylsilacyclopentane is representative of this class of compounds. Preliminary data for the
Priya Saini et al.
World journal of microbiology & biotechnology, 33(5), 82-82 (2017-04-06)
In order to produce enantiomerically pure epoxides for the synthesis of value-added chemicals, a novel putative epoxide hydrolase (EH) sgeh was cloned and overexpressed in pET28a/Escherichia coli BL21(DE3). The 1047 bp sgeh gene was mined from Streptomyces griseus NBRC 13350 genome
Exibir todos os documentos relacionados

Questions

Reviews

No rating value

Active Filters

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica