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4440-65-7

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4440-65-7 Usage

Chemical Properties

3-Hexenal has a natural green, fruity, apple-like odor

Occurrence

Reported found in apple, banana, mandarin juice, guava, feyoa fruit, melon, raspberry, strawberry, sweet pepper, tomato and tomato paste, ginger, butter and beer

Definition

ChEBI: A hexenal carrying an unsaturation at position 3.

Aroma threshold values

Detection: 0.25 to 3 ppb; aroma characteristics at 1.0%: sharp penetrating leafy green, vegetative stemmy with unripe tomato, melon and tropical nuances.

Taste threshold values

Taste characteristics at 1 to 10 ppm: strong, aromatic green, with waxy vegetative green melon and tomato nuances and a hint of cinnamon spice.

Check Digit Verification of cas no

The CAS Registry Mumber 4440-65-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4440-65:
(6*4)+(5*4)+(4*4)+(3*0)+(2*6)+(1*5)=77
77 % 10 = 7
So 4440-65-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O/c1-2-3-4-5-6-7/h3-4,6H,2,5H2,1H3/b4-3+

4440-65-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hexenal

1.2 Other means of identification

Product number -
Other names 3-HEXENAL

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:4440-65-7 SDS

4440-65-7Relevant articles and documents

-

Winter,M.

, p. 1754 - 1760 (1963)

-

Selective reduction of carboxylic acids to aldehydes catalyzed by B(C 6F5)3

Bezier, David,Park, Sehoon,Brookhart, Maurice

supporting information, p. 496 - 499 (2013/03/29)

B(C6F5)3 efficiently catalyzes hydrosilylation of aliphatic and aromatic carboxylic acids to produce disilyl acetals under mild conditions. Catalyst loadings can be as low as 0.05 mol %, and bulky tertiary silanes are favored to give selectively the acetals. Acidic workup of the disilyl acetals results in the formation of aldehydes in good to excellent yields.

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