Online Database of Chemicals from Around the World

DL-Malic acid
[CAS# 6915-15-7]

List of Suppliers
Qingdao Free Trade Zone United International Co., Ltd. China Inquire  
+86 (532) 83893696
+86 13808950921
jason.wang@unitedint.com
QQ chat
Chemical distributor
chemBlink standard supplier since 2006
Zhejiang Chemicals Import & Export Corporation China Inquire  
+86 (571) 8704-3117
8704-9996
info@zhechem.com
Chemical distributor
chemBlink standard supplier since 2007
Baoji Herbest Bio-tech Co., Ltd. China Inquire  
+86 (917) 888-1635
root@herbest.cn
QQ chat
Chemical manufacturer since 2008
chemBlink standard supplier since 2008
Simagchem Corporation China Inquire  
+86 13806087780
sale@simagchem.com
Chemical manufacturer since 2002
chemBlink standard supplier since 2008
Extrasynthese Chemical S.A.S. France Inquire  
+33 (47) 898-2034
info@extrasynthese.com
Chemical manufacturer
chemBlink standard supplier since 2009
Hefei TNJ Chemical Industry Co., Ltd. China Inquire  
+86 (551) 6541-8684
sales@tnjchem.com
Chemical manufacturer since 2001
chemBlink standard supplier since 2010
Changmao Biochemical Engineering Co., Ltd. China Inquire  
+86 (519) 8577-6811
sales@cmbec.com
Chemical manufacturer since 1992
chemBlink standard supplier since 2010
Alfa Chemistry USA Inquire  
+1 (201) 478-8534
inquiry@alfa-chemistry.com
Chemical distributor since 2012
chemBlink standard supplier since 2012
Complete supplier list of DL-Malic acid
Identification
Classification Chemical reagent >> Organic reagent >> Fatty acid
Name DL-Malic acid
Synonyms DL-Hydroxysuccinic acid; DL-2-Hydroxybutanedioic acid; DL-Apple acid
Molecular Structure CAS # 6915-15-7 (617-48-1), DL-Malic acid, DL-Hydroxysuccinic acid, DL-2-Hydroxybutanedioic acid, DL-Apple acid
Molecular Formula C4H6O5
Molecular Weight 134.09
CAS Registry Number 6915-15-7 (617-48-1)
EC Number 230-022-8
SMILES C(C(C(=O)O)O)C(=O)O
Properties
Solubility 0.5 M (water, 20 ºC)
Density 1.609 g/mL
Melting point 130 ºC
Boiling point 150 ºC (decomp.)
Flash point 203 ºC
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319    Details
Precautionary Statements P264-P264+P265-P280-P302+P352-P305+P351+P338-P321-P332+P317-P337+P317-P362+P364    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Eye irritationEye Irrit.2H319
Skin irritationSkin Irrit.2H315
Serious eye damageEye Dam.1H318
Acute toxicityAcute Tox.4H302
Specific target organ toxicity - single exposureSTOT SE3H335
Acute toxicityAcute Tox.4H303
Skin sensitizationSkin Sens.1H317
SDS Available
up Discovory and Applicatios
Malic acid, a naturally occurring organic compound, was first isolated in 1785 by Swedish chemist Carl Wilhelm Scheele from unripe apples. The name malic is derived from the Latin word malum, meaning apple, reflecting its natural source. Scheele�s discovery marked a significant advancement in organic chemistry, as malic acid became one of the earliest identified plant acids. Its chemical structure was later elucidated in the 19th century, revealing that malic acid is a dicarboxylic acid with two functional carboxyl groups. This compound plays a crucial role in the citric acid cycle (Krebs cycle), which is vital for cellular respiration in all aerobic organisms. Today, malic acid is recognized for its versatile applications in food, medicine, and cosmetics due to its tart flavor and beneficial properties.

Malic acid is extensively used in the food industry as an acidulant to enhance flavor and preserve the freshness of various products. Its naturally tart taste is ideal for balancing sweetness and adding a tangy flavor to beverages, candies, and dairy products. In soft drinks and fruit juices, malic acid provides a longer-lasting sour taste compared to citric acid. It also acts as a pH regulator and preservative, helping to extend the shelf life of processed foods. Additionally, malic acid is used in confectionery to create sour candies and in baked goods to improve dough strength and texture.

Malic acid is incorporated into nutritional supplements due to its role in the citric acid cycle, where it helps produce energy by aiding in the conversion of carbohydrates, fats, and proteins into carbon dioxide and water. This property makes malic acid a valuable component in energy-boosting supplements. It is also included in formulations for managing conditions like fibromyalgia and chronic fatigue syndrome (CFS), as it may help alleviate muscle fatigue and improve stamina.

In cosmetics, malic acid serves as an alpha-hydroxy acid (AHA), known for its exfoliating properties. It is commonly used in skincare products to promote the shedding of dead skin cells, enhance skin texture, and improve overall complexion. Malic acid helps in reducing the appearance of fine lines, wrinkles, and hyperpigmentation, making it a key ingredient in anti-aging treatments. Its ability to maintain skin hydration and stimulate collagen production further supports its use in moisturizers and peels.

Malic acid has therapeutic applications in oral health care. It is included in toothpaste and mouthwashes for its ability to stimulate saliva production, which helps maintain oral hygiene and prevent dry mouth. Additionally, malic acid's mild antimicrobial properties contribute to its use in treating bad breath and oral infections. Its role in the citric acid cycle also supports its use in managing metabolic acidosis, a condition where the body produces excessive acid or when the kidneys are not removing enough acid from the body.

In agriculture, malic acid is used to adjust soil pH, making it more conducive to plant growth. It can act as a chelating agent, helping to make essential minerals more available to plants. In environmental applications, malic acid helps in metal cleaning and as a natural descaling agent due to its ability to dissolve mineral deposits.

Malic acid is employed in various industrial processes. It is used in the production of biodegradable polymers and plasticizers. It also serves as a buffering agent in pharmaceutical formulations, helping to stabilize the pH and enhance the solubility of active ingredients.

References

2024. The role of citric acid and enzyme activities on sourness in pineapple fruit after low temperature storage. Horticulture, Environment, and Biotechnology, 65(6).
DOI: 10.1007/s13580-024-00660-0

1998. Mechanism of the Protective Effect of Sodium Malate on Cisplatin-Induced Toxicity in Mice. Biological and Pharmaceutical Bulletin, 21(2).
DOI: 10.1248/bpb.21.121

1984. Kinetic mechanism in the direction of oxidative decarboxylation for NAD-malic enzyme from Ascaris suum. Biochemistry, 23(22).
DOI: 10.1021/bi00318a011
Market Analysis Reports
List of Reports Available for DL-Malic acid
Related Products
Maltotriitol  D-Maltotriose  4-Maleimidophenol  4-Maleimidophenyl isocyanate  3-Maleimidopropionic acid  11-Maleimidoundecanoic acid  N-kappa-Maleimidoundecanoic acid hydrazide trifluoroacetate  Malformin C  D(+)-Malic acid  L(-)-Malic acid  D-(+)-Malic acid diethyl ester  Malic acid dioctyl ester  DL-Malic acid disodium salt  Malic acid 4-methyl ester  Mallorepine  Malonaldehyde bis(diethyl acetal)  Malonaldehyde bis(phenylimine) dihydrochloride  Malonaldehyde bis(phenylimine) monohydrochloride  Malonamide  Malonic acid-d4