Y0001304

Butyl methanesulfonate

Name: Butyl methanesulfonate
Brand: SIAL
Price: 241 USD
Availability: InStock

European Pharmacopoeia (EP) Reference Standard

Synonym(s):

NSC 36060

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About This Item

Empirical Formula (Hill Notation):

C₅H₁₂O₃S

CAS Number:

1912-32-9

Molecular Weight:

152.21

UNSPSC Code:

41116107

NACRES:

NA.24

Key Documents

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Product Name

Butyl methanesulfonate, European Pharmacopoeia (EP) Reference Standard

SMILES string

[S](=O)(=O)(OCCCC)C

InChI

1S/C5H12O3S/c1-3-4-5-8-9(2,6)7/h3-5H2,1-2H3

InChI key

LFLBHTZRLVHUQC-UHFFFAOYSA-N

grade

pharmaceutical primary standard

API family

imatinib

manufacturer/tradename

EDQM

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

Related Categories

Analytical Reference Materials for Pharma QC

Pharmacopeia & Metrological Institute Standards

Reference Materials

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1 of 4

This Item	Y0001487	B1217000	D1700000
Y0001304 Butyl methanesulfonate	Y0001487 Butyl methacrylate	B1217000 Butyl parahydroxybenzoate	D1700000 Diethylstilbestrol monomethyl ether
grade pharmaceutical primary standard	grade pharmaceutical primary standard	grade pharmaceutical primary standard	grade pharmaceutical primary standard
manufacturer/tradename EDQM	manufacturer/tradename EDQM	manufacturer/tradename EDQM	manufacturer/tradename EDQM
format neat	format neat	format neat	format neat
application(s) pharmaceutical (small molecule)	application(s) pharmaceutical (small molecule)	application(s) pharmaceutical (small molecule)	application(s) pharmaceutical (small molecule)
API family imatinib	API family butylated methacrylate copolymer	API family butylparaben	API family diethylstilbestrol
storage temp. 2-8°C	storage temp. 2-8°C	storage temp. 2-8°C	storage temp. 2-8°C

Application

Butyl methanesulfonate EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

General description

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.

Other Notes

Sales restrictions may apply.

Packaging

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

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Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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In vitro reaction of N-n-butyl-N-nitrosourea and n-butyl methanesulphonate with guanine and thymine bases of DNA.

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

Effects of carcinogen and/or mutagen on normal and gonatotropin-primed ovaries of mice.

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

Mutagenicity and induction of sister chromatid exchange by optically active enantiomers of secondary butyl methanesulfonate.

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

Cell-cycle dependent mutation of human lymphoblasts: bromodeoxyuridine and butyl methanesulfonate.

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

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