Y0001304
Butyl methanesulfonate
European Pharmacopoeia (EP) Reference Standard
Sinonimo/i:
NSC 36060
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About This Item
Formula empirica (notazione di Hill):
C5H12O3S
Numero CAS:
Peso molecolare:
152.21
Codice UNSPSC:
41116107
NACRES:
NA.24
Prodotti consigliati
Grado
pharmaceutical primary standard
Famiglia di API
imatinib
Produttore/marchio commerciale
EDQM
applicazioni
pharmaceutical (small molecule)
Formato
neat
Temperatura di conservazione
2-8°C
InChI
1S/C5H12O3S/c1-3-4-5-8-9(2,6)7/h3-5H2,1-2H3
LFLBHTZRLVHUQC-UHFFFAOYSA-N
Descrizione generale
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.
Applicazioni
Butyl methanesulfonate EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.
Confezionamento
The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.
Altre note
Sales restrictions may apply.
Prodotti correlati
N° Catalogo
Descrizione
Determinazione del prezzo
Codice della classe di stoccaggio
10 - Combustible liquids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
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I clienti hanno visto anche
H Hoppe et al.
Mutation research, 250(1-2), 411-421 (1991-09-11)
Cells of the human lymphoblast line WI-L2 and its derivative TK-6 were synchronized by centrifugal elutriation and cell-cycle dependent mutation to 6TGR (HPRT) and OUAR (Na+, K+ ATPase) measured. Bromodeoxyuridine induced 6TGR and OUAR mutations within S phase while butylmethyl-sulfonate
J C Ball et al.
Environmental and molecular mutagenesis, 13(2), 100-106 (1989-01-01)
This report describes experiments in which a chiral alkyl methanesulfonate was used to investigate possible mechanisms by which alkylating agents cause their mutagenic, cytotoxic, and clastogenic effects. Optically active enantiomers and the racemic mixture of 2-butyl methanesulfonate (2-BMS) were cytotoxic
A R Rao
International journal of cancer, 28(1), 105-110 (1981-07-15)
The influence of pregnant mare serum gonadotropin (PSGM) on the induction of ovarian tumors by carcinogen(DMBA) and/or mutagens (EMS and BMS) has been studied in Swiss albino mice. Priming of the ovaries of 6-week-old mice with PMSG (50 IU/mouse) 24
R Saffhill
Carcinogenesis, 5(5), 621-625 (1984-05-01)
The reaction of N-n-butyl-N-nitrosourea ( BNU ) and n-butyl methanesulphonate (BMS) with DNA has been investigated. In addition to the expected n- butylpurines formed on reaction with BNU some rearranged sec-butyl-adducts were also observed, indicating that a carbonium ion is
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