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过氧化苯甲酰

FAO/WHO食品添加剂联合专家委员会(JECFA)2000年第55次会议通过,并出版在(联合国粮农组织)《食品与营养文集》(FNP)2000年第52期附录8,取代了FAO/WHO食品添加剂联合专家委员会1975年第19次会议通过的,并刊登在核磁共振谱(NMRS)1976年第55条和《食品与营养文集》1992年第52期中的阐述。FAO/WHO食品添加剂联合专家委员会在1963年第7次会议提出了人用小麦粉的允许处理量为0~40mg/kg(特殊条件下为40~75mg/kg),但是没有充分的依据。

又名           过氧化苯甲酰,联合国食品法典委员会(INS)国际编号928

定义      

化学名称        过氧化二苯(甲)酰

化学文摘(C.A.S.)编号    94-36-0

化学式              C14H10O4

结构式    

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分子量       242.23

测定         其含量不少于96.0%

状态         无色,透明固体,略带苯甲醛气味。注意:过氧化苯甲酰是一种高活性化合物,易燃易爆。

用途         面粉处理剂

特性

鉴定

溶解性(FNP 5 不溶于水,微溶于乙醇,易溶于乙醚。

熔化范围        103~106℃分解

分解为苯甲酸      0.5g过氧化物中加50ml 0.5N氢氧化钾乙醇溶液,逐渐加热至沸,持续15分钟,冷却,用200ml水稀释,然后加入足量0.5N盐酸以增强溶液酸性,用乙醚萃取,乙醚溶液经无水硫酸钠干燥,在蒸气池中脱水浓缩。在121~123℃下,苯甲酸的残余物溶解。

纯度

        含量不超过2mg/kg

                通过原子吸收方法测定以达到规定要求。样品数量的选取以及预处理方法一般按照FNP 5“仪器操作方法”规定进行。

分析方法        100ml具塞锥形瓶中,用15ml丙酮溶解250mg样品(准确称取),再加50%w/v)碘化钾溶液3ml,摇匀1分钟,立即用0.1N硫代硫酸钠标准溶液滴定。(不需要加入淀粉作为指示剂)。每毫升0.1N硫代硫酸钠相当于12.11mg过氧化苯甲酰。

BENZOYL PEROXIDE

Prepared at the 55 th JECFA2000and published in FNP 52 Add 82000),superseding specifications prepared at the 19 th JECFA1975),published in NMRS 55B 1976and in FNP 521992.The 7 th JECFA1963had insufficient data to establish an estimate of an acceptable level of treatment of 0-40 mg/kg of flour for human consumption conditional acceptance for special purposes 40-75mg/kg .

SYNONYMS      Benzoyl superoxide , INS No.928

DEFINITION

Chemical names    Dibenzoyl peroxide

C.A.S.number      94-36-0

Chemical formula    C14H10O4

Structural formula    

                      

Formula weight      242.23

Assay              Not less than 96.0%

DESCRIPTION      Colourless , crystalline solid having a faint odour of benzaldehyde.

                   Caution :Benzoyl peroxide is a highly reactive compound and may five rise to explosions

FUNCTIONAL USES   Flour treatment agent

CHARACTERISTICS  

IDENTIFICATION

Solubility (FNP 5)     Insoluble in water, slightly soluble in ethanol, soluble in ether

Melting range (FNP 5) 103-106ºwith decomposition

Decomposition to      To 0.5g of the sample peroxide add 5o ml of 0.5 N

benzoic acid        ethanolic potassium hydroxide, heat gradually to boiling and continue boiling for 15min .Cool and dilute with 200ml of water. Add sufficient 0.5N hydrochloric acid to make strongly acidic and extract with ether. Dry the ether solution over anhydrous sodium sulfate, and then evaporate to dryness on a steam bath. The residue of benzoic acid so obtained melts between 121ºand 123º.

PURITY

Lead               Not more than 2mg/kg

                   Determine using an atomic absorption technique appropriate to the specified level. The selecton of sample size and method of sample preparation may be based on the principles of the method described in FNP 5, “Instrumental Methods ”.

METHOD OF ASSAY Dissolve about 250 mg of the sample, accurately

                    Weighed, in 15ml of acetone in a 100-ml glass-stoppered bottle. Add 3 ml of 50% (w/v)

                   Potassium iodide solution and swirl for 1min.Titrate immediately with 0.1N sodium thiosulfate (without addition of starch as an indicator). Each ml of 0.1N sodium thiosulfate is equivalent to 12.11mg of C14H10O4