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Detail of > 14901-07-6

  • CAS Number:
  • 14901-07-6
  • Name:
  • 3-Buten-2-one,4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-

  • Superlist Name:
  • Irisone
  • Formula:
  • C13H20O
  • Molecular Structure:
  • Synonyms:
  • 4-(2,6,6-Trimethyl-1-cyclohexen-1-yl)-3-buten-2-one;4-(2,6,6-Trimethyl-1-cyclohexenyl)-3-buten-2-one;NSC 402758;NSC 46137;
  • Molecular Weight:
  • 192.30
  • EINECS:
  • 238-969-9
  • Density:
  • 0.944 g/cm3
  • Melting Point:
  • -49 °C
  • Boiling Point:
  • 254.8 °C at 760 mmHg
  • Flash Point:
  • 121.3 °C
  • Solubility:
  • slightly soluble in water
  • Appearance:
  • clear slightly yellow to yellow liquid
  • Hazard Symbols:
  • IrritantXi, DangerousN
  • Risk Codes:
  • 38-51/53-36/37/38
  • Safety:
  • 61-36/37/39-27-26Details
  • Transport Information:
  • UN 3082 9/PG 3
  • particular:
  • particular
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14901-07-6 IrisoneCompetitive Product

Assay:97%
China (Mainland)   3216
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14901-07-6 IrisoneCompetitive Product

Beta-Ionone
China (Mainland)   HALAL ISO KOSHER  3194
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  • Address:No. 189, Fengqi East Road, Hangzhou, China
MSN:caiyi9@hotmail.com

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beta-Ionone FEMA:2595
China (Mainland)   2958
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  • Address:B/2601 Fuli Building, 328# WenEr Rd. Hangzhou City 310012 China

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Irisone
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  • Address:Room 804 Unit 2 Tower 1 Jinyinhucaifu Building , Jinyinhu No.18, Dongxihu District, Wuhan , China

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Beta Ionone
India   60
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  • Address:4703, 4704 & 4705/1/2, 3 & 4, G.I.D.C.,

CAS No. 

14901-07-6 Irisone

OCCURANCE It has been reported as constituent of oil of boronia. ODOUR Pleasant odour COLOR & APPEARANCE Pale yellow liquid. STABILITY & DISCOLORATION Stable, not known to cause discoloration. REFRACTIVE INDEX AT 20?/sup>C 1.5190 - 1.5215 ALPHA IONONE CONTENT Max. 1% b
India  
  • Tel:+ 91 - 7104 - 237627
  • Address:W-36, MICD, HINGNA ROAD, NAGPUR - 440 016, (M.S.) , INDIA

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β-Ionone Natural
China (Mainland)   180
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  • Address:No. 317, 219 Nong, Gao Muqiao Road, Zhangjiang Hightech. Park, Pudong, Shanghai

CAS No. 

14901-07-6 Irisone

C13H20O
China (Mainland)  
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  • Address:Room1518 HuaQiao Hotel, No.15 Xinxing Dongxiang, Xicheng District Beijing

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Natural ionone beta
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  • Address:18F-B4, Shangmao Century Plaza No.49 Zhongshan South Road, Nanjing, Jiangsu, china

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United States  
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  • Address:1050 Cypress Creek Rd Oakdale, LA 71463 877-NAT-FLAV

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Japan  
  • Tel:+81-3-5744-0511
  • Address:Nissey Aroma Square 17F 5-37-1, Kamata, Ohta-ku, Tokyo 144-8721, Japan

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United States  
  • Tel:(513) 881-7144
  • Address:9047 Sutton Place Hamilton, Ohio 45011

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  • Address:Plot No. A - 42,Street No.2,M.I.D.C.,Andheri (East),Mumbai,Maharashtra,Pin - 400 093,INDIA.

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  • Tel:+912225343931
  • Address:Mumbai Agra Road Balkum, Thane - 400 608

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China (Mainland)  
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  • Address:guangzhou

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  • Address:201room,46building,chengbeixingchen tongan district,xiamen

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China (Mainland)   6
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  • Address:4Des Yongling road,Jiangkou Development Area of huangyan City, Zhejiang 318020 P.R. of China

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United States   10
  • Tel:201-784-6100
  • Address:Norwood, New Jersey 07648-2002
  • Total:20 Page 1 of 1 1
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    Reference

    Perfume and/or flavoring materials
    Perfume and/or flavoring materials. Naegeli, Peter (Givaudan, L., et Cie. S. A., Switz.). Ger. Offen. DE 2610238 23 Sep 1976, 20 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C07D307-94. PRIORITY: CH 75-3053 11 Mar 1975. DOCUMENT TYPE: Patent CA Section: 62 (Essential Oils and Cosmetics) Section cross-reference(s): 17, 27 Theaspirane (I) [36431-72-8], which occurs in trace amts. in certain essential oils, has a fresh, fruity odor useful in perfumes and flavorings as principal component or modifier. For example, a vanilla flavoring contg. guaiacol 1.0, heliotropin 1.0, isoeugenol 2.0, p-hydroxybenzaldehyde 3.0, vanillin 20.0, ethylvanillin 120.0, I 3.0, and EtOH 850.0 parts had an odor superior to that of a similar compn. lacking I. To prepare I, .beta.-ionone [14901-07-6] was treated with isopropenyl acetate [108-22-5] to form 4-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)-2-acetoxybut-2-ene [61693-39-8], reduced with NaBH4 to 4-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)butan-2-ol [61693-40-1], and cyclized by refluxing with p-toluenesulfonic acid in C6H6.
    Carotenogenesis: Possible mechanism of action of trisporic acid in Blakeslea trispora
    Carotenogenesis: Possible mechanism of action of trisporic acid in Blakeslea trispora. Rao, Satya; Modi, V. V. (Fac. Sci., Maharaja Sayajirao Univ. Baroda, Baroda, India). Experientia, 33(1), 31-3 (English) 1977. CODEN: EXPEAM. DOCUMENT TYPE: Journal CA Section: 3 (Biochemical Interactions) Trisporic acid (I) [11043-91-7] and .beta.-ionone [14901-07-6], stimulators of carotenogenesis in B. trispora, were competitive, suggesting that they have the same site of action. Since .beta.-ionone has been reported to act on the biochem. pathway of terpenoid synthesis between the conversion of 5-phosphomevalonate to dimethyl allyl pyrophosphate, I may well act by derepressing the enzymes involved in this conversion. The minus strain of B. trispora was selected as the test organism, because it does not produce I but carotene synthesis was stimulated by I.

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