[citation needed]. Benzaldehyde (C6H5CHO) is a chemical compound consisting of a benzene ring with an aldehyde substituent. 3 Chemical and Physical Properties Expand this section. 0000002830 00000 n Benzaldehyde dimethyl acetal used as an effective reagent for the construction of selenocarbonyl compounds. trailer 15 22 0000001357 00000 n 0000010393 00000 n Reaction of benzaldehyde with anhydrous sodium acetate and acetic anhydride yields cinnamic acid, while alcoholic potassium cyanide can be used to catalyze the condensation of benzaldehyde to benzoin. Safety Information. 0000000016 00000 n Your browser does not support JavaScript. 2 Names and Identifiers Expand this section. Contents. Packaging 100, 500 g in glass bottle Safety & Documentation.

Boiling Point (°C) 0 - 100 (31) 101 - 200 (95) 201 - 300 (56) 301 - 400 (3) 1001+ (1) Melting Point (°C) less than 0 (18) 0 - 100 (156) 101 - 200 (70) 201 - 300 (13) 301 - 400 (2) 1001+ (1) Color. 3-acetyl-benzaldehyde.

Benzaldehyde is an F.D.A. 0000009302 00000 n 0000000945 00000 n Create . While it is commonly employed as a commercial food flavourant (almond flavour) or industrial solvent, benzaldehyde is used chiefly in the synthesis of other organic compounds, ranging from pharmaceuticals to plastic additives. Reaction of benzaldehyde with anhydrous sodium acetate and acetic anhydride yields cinnamic acid, whil… Since the boiling point of benzoic acid is much higher than that of benzaldehyde, it may be purified by distillation. 2 Names and Identifiers Expand this section. Find out more about the company LUMITOS and our team. Benzaldehyde can be oxidized to benzoic acid; in fact "[B]enzaldehyde readily undergoes autoxidation to form benzoic acid on exposure to air at room temperature" causing a common impurity in laboratory samples.

Hazard statements H302. More... Molecular Weight: 148.16 g/mol. Benzaldehyde (C 6 H 5 CHO) is a chemical compound consisting of a benzene ring with an aldehyde substituent. However, the chemicals are not in widespread use because they damage vegetation and contaminate water supplies.

It is also an important intermediate for the processing of perfume and flavouring compounds and in the preparation of certain aniline dyes. Signal word Warning. 0000000736 00000 n

It is a member of benzaldehydes and a monomethoxybenzene. Benzaldehyde, 2-bromo-Benzaldehyde, o-bromo-More... Molecular Weight: 185.02 g/mol. 0000002609 00000 n 15 0 obj<> endobj

1 Structures Expand this section. %PDF-1.4 %����

0000010635 00000 n The Technical grade is a versatile chemical intermediate in the manufacture of pharmaceuticals, dyes, perfume and flavoring chemicals. 0000006633 00000 n It is the simplest representative of the aromatic aldehydes and one of the most industrially used members of this family of compounds. It is the primary component of bitter almond oil extract, and can be extracted from a number of other natural sources in which it occurs, such as apricot, cherry, and laurel leaves, peach seeds and, in a glycoside combined form (amygdalin), in certain nuts and kernels. To use all functions of this page, please activate cookies in your browser.

4 Spectral Information Expand this section. Q�=+��‚̓���6���2�\NUzi�Ra�����Hx��~�WzshN6�n��W�k���ٮ�d����������#\S���E�p���)���V鷯��,���'p&�O���?w����c��eT�w��]I�@�sQ�BP^���r�b�4��� ����l��,v�Ы�s(Ph'I�Ln��qJ��q��:�)FQTǕ�a�3GRԦZ�0zҭ�C�b&���MD��V�Ӏ{�S��XθO�6�\X������!L��C��J��b��1�W�q22��,Y������@��.rl��~�C@�Q�Q�B��m͂��tH�����C)v [�P�������E�xL���׏Z��TBR5�C�)�m5�.m㗤�I����׎����7� To use all the functions on Chemie.DE please activate JavaScript. 0000002531 00000 n 0000001154 00000 n Benzyl alcohol can be formed from benzaldehyde by means of hydrogenation. (The scheme above depicts only one of the two formed enantiomers). 0000006396 00000 n %%EOF

6 Chemical Vendors. 5 Related Records Expand this section.

4 Spectral Information Expand this section. 17 0 obj<>stream colorless (1) orange (1) white (2) yellow (5) Reaction Suitability .

0000005643 00000 n Currently liquid phase chlorination or oxidation of toluene are among the most used processes. Dates: Modify . Dates: Modify: 2020-09-19.

xref There are also a number of discontinued applications such as partial oxidation of benzyl alcohol, alkali treating of benzal chloride and reaction between benzene and carbon monoxide. With an accout for my.chemeurope.com you can always see everything at a glance – and you can configure your own website and individual newsletter.
Read what you need to know about our industry portal chemeurope.com.

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�U���2������#A@�OY`|n��I�_ �p�0z�')ga 0000002906 00000 n �PEuG�BXI�;���8@H�V(����nŇ�T��� ��bӣ���Igك�D�{a-Xx�3��f���H��+�9���eO�d�g3�X����e��I���I���i��G�W��l�y-T�v�s�vcV6\��#�e�V��n/�f����a���i��zC�u��ڮ17m7�,���j|��С%9L�4��_W�y�]L ��O�냟0\���ǂH���o���{�h�;"�F�d���z=�Q�!��}����Y���j\�A>P�Q�~Wݣe6��d��J�>��@�j .y�j�EK���d��6SJ�ʄ�U��b��v�t��@J���%d�%���CͿP&R�C�[Ny8'E���[�^�7�"��� ��B�%����#,��D�W�cx\.��㑚�쾘(#)W(�GO�(���T�s8�3�b\���s�Z`��\*�{�f��"���*SJ�/��6n���6A���Oj�>��I&0��I������K��n_��9(�"p��F0y Yh�;�u�Iʮ��ܝx06\��)�����G$�Z�*tq �R�z�-ᤁ��Q�Nzw1�;���M#*��-d�bh3�����`l>�-.��G��L��=&� ��vER�[�TX'PӲ�յ"=�P�=��[��%�$��ՠ���$�A�D�d�#���/Ȳ��#�M'�4�cO�"0w��p�|��c -�ʅ��m̂���O\xB�roy"����D;���3��ϾCVTL�Yd{�~��3*t���~$��/$"6iA��֖��p��P�-��T2�=>,(c'�TK�H��-�c����ei�e�VƘ.��^�d��u\��U�Yoa�~掇�I���%Q�n�r솾���?FI�|F. It has a role as a Brassica napus metabolite.

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0000005199 00000 n

0000001949 00000 n <]>> Categories: Aldehydes | Aromatic compounds | Solvents | DEA List I chemicals. 6 Chemical Vendors. 0000010154 00000 n 2020-10-24. Almonds, apricots, apples and cherry kernels, contain significant amounts of amygdalin. Benzaldehyde can be obtained by many processes. startxref 2005-03-26.

The synthesis of mandelic acid starts from benzaldehyde: First hydrocyanic acid is added to benzaldehyde and the resulting mandelic acid nitrile is subsequently hydrolysed to a racemic mixture of mandelic acid.

This treatment may prevent avalanches caused by unstable depth hoar layers.

TYPICAL PHYSICAL PROPERTIES OF BENZALDEHYDE: BOILING POINT 179° C @ 760 mm Hg

1 Structures Expand this section. Create: 2006-01-25. 7 Literature Expand this section.

2 Names and Identifiers Expand this section. 0000005870 00000 n 0 Symbol GHS07. The speed of this reaction depends on the substituents present in the aromatic ring. Find out how LUMITOS supports you with online marketing.

H��W]s��}�Wt��V��j�[��4U�� a������8� )�z�P^�'�t�B0v6��m�{����~��՘�Ǽ�J�I� #�C�9�����Yy>�D���_6.۹$�\�pH>]5l�s8������[�e/������1�����f�φP�!x&��&?���@��S�A��{��m � Currently benzaldehyde is primarily made from toluene by a number of different processes.

At room temperature it is a colorless liquid with a characteristic and pleasant almond-like odor: benzaldehyde is an important component of the scent of almonds, hence its typical odor.

Benzyl alcohol can be formed from benzaldehyde by means of hydrogenation or by treating the compound with alcoholic potassium hydroxide thus undergoing a simultaneous oxidation and reduction which result in the production of potassium benzoate and benzyl alcohol. Glaciologists LaChapelle and Stillman reported in 1966 that benzaldeyde and N-heptaldehyde inhibit the recrystallization of snow and therefore the formation of depth hoar. ChEBI. 3-methoxybenzaldehyde is a member of the class of benzaldehydes in which the hydrogen at position 3 of benzaldehyde has been replaced by a methoxy group. © 1997-2020 LUMITOS AG, All rights reserved, https://www.chemeurope.com/en/encyclopedia/Benzaldehyde.html, Your browser is not current. This glycoside breaks up under enzyme catalysis into benzaldehyde, hydrocyanic acid and two molecules of glucose. Precautionary statements P301 + P312 + P330. Benzaldehyde can also undergo disproportionation in concentrated alkali (Cannizzaro's reaction): one molecule of the aldehyde is reduced to the corresponding alcohol and another molecule is simultaneously oxidized to the salt of a carboxylic acid. Contents. On oxidation, benzaldehyde is converted into unpleasant smelling benzoic acid. 3 Chemical and Physical Properties Expand this section. sanctioned synthetic flavoring substance (21 CFR § 182.60) generally recognized as safe for foods (GRAS). Contents.

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