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(7E)-dodec-7-enal, a member of the aldehyde family, is a colorless liquid with a strong, fruity odor. It is naturally found in various fruits and plants, contributing to their characteristic aroma. (7E)-dodec-7-enal is also recognized for its potential antimicrobial and antioxidant properties, which makes it a promising candidate for pharmaceutical and cosmetic applications.

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  • 63851-40-1 Structure
  • Basic information

    1. Product Name: (7E)-dodec-7-enal
    2. Synonyms: (E)-7-Dodecenal
    3. CAS NO:63851-40-1
    4. Molecular Formula: C12H22O
    5. Molecular Weight: 182.3025
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 63851-40-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 261.7°C at 760 mmHg
    3. Flash Point: 112.7°C
    4. Appearance: N/A
    5. Density: 0.837g/cm3
    6. Vapor Pressure: 0.0114mmHg at 25°C
    7. Refractive Index: 1.444
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (7E)-dodec-7-enal(CAS DataBase Reference)
    11. NIST Chemistry Reference: (7E)-dodec-7-enal(63851-40-1)
    12. EPA Substance Registry System: (7E)-dodec-7-enal(63851-40-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 63851-40-1(Hazardous Substances Data)

63851-40-1 Usage

Uses

Used in the Food Industry:
(7E)-dodec-7-enal is used as a flavoring agent for its strong, fruity odor, enhancing the sensory experience of various food products.
Used in Perfumery and Fragrance Industry:
(7E)-dodec-7-enal is used as a component in the production of perfumes and fragrances, where it contributes to the overall scent profile, adding a fresh and fruity note to the blend.
Used in Pharmaceutical Applications:
(7E)-dodec-7-enal is studied for its potential antimicrobial properties, which could make it useful as an additive in the pharmaceutical industry to prevent the growth of harmful microorganisms in certain products.
Used in Cosmetic Applications:
The antioxidant properties of (7E)-dodec-7-enal are being explored for its potential use in the cosmetic industry, where it could help protect products from oxidation and extend their shelf life, as well as provide benefits to the skin when used in topical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 63851-40-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,5 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63851-40:
(7*6)+(6*3)+(5*8)+(4*5)+(3*1)+(2*4)+(1*0)=131
131 % 10 = 1
So 63851-40-1 is a valid CAS Registry Number.

63851-40-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-7-Dodecen-1-al

1.2 Other means of identification

Product number -
Other names (Z)-Dodec-7-enal

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:63851-40-1 SDS

63851-40-1Downstream Products

63851-40-1Relevant articles and documents

Pheromone Evaluation of Four Geometric Isomers of 4,11-Hexadecadienal toward Male Eri-Silk Moths

Tomida, Ichiro,Mayesawa, Tsuneaki

, p. 1962 - 1965 (2007/10/02)

Four geometric isomers of 4,11-hexadecadienal were prepared and their pheromone activities to male eri-silk moths were evaluated by using the fluttering test and electro-antennography.None of these compounds showed any activity in spite of their similar structure to other pheromone mimics and to the natural pheromone.These results suggest that the presence of 6,11-double bonds is essential for pheromone activity.

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