Dodecanedioic acid
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Dodecanedioic acid
structure -
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CAS No:
693-23-2
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Formula:
C12H22O4
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Chemical Name:
Dodecanedioic acid
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Synonyms:
Dodecanedioic acid;1,10-Decanedicarboxylic acid;1,12-Dodecanedioic acid;Decamethylenedicarboxylic acid;1,10-Dicarboxydecane;n-Dodecanedioic acid;SL-AH;Corfree M 2;n-Dodecane-α,ω-dioic acid;NSC 400242;LCA 141;142610-44-4;91485-80-2
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CAS No:
Description
Dodecanedioic acid (C12) is a dicarboxylic acid which is a water-soluble substance with a metabolic pathway intermediate to those of lipids and carbohydrates.
PelletsLargeCrystals|Solid
Dodecanedioic acid is an alpha,omega-dicarboxylic acid that is dodecane in which the methyl groups have been oxidised to the corresponding carboxylic acids. It has a role as an EC 1.1.1.1 (alcohol dehydrogenase) inhibitor and a human metabolite. It is an alpha,omega-dicarboxylic acid and a lipid. It is a conjugate acid of a dodecanedioate(2-). It derives from a hydride of a dodecane.
Dodecanedioic acid Basic Attributes
230.30100
230.30
211-746-3
978YU42Q6I
400242
DTXSID3027297
2917190090
Characteristics
74.60000
3.2
1.15
130-132 °C
205-210 °C @ Press: 1 Torr
220ºC
1.475
< 0.1 g/L (20 ºC)
-20ºC
21 mm Hg ( 222 °C)
Safety Information
NONH for all modes of transport
R36/37/38
S24/25
Xi
Stable. Incompatible with strong oxidizing agents, reducing agents. Combustible.
P305 + P351 + P338
H319
|Warning|H315 (11.14%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 476 companies from 11 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Toxicity
AT 1.0 MMOL, DICARBOXYLIC ACIDS DECR THE NEUROMUSCULAR INHIBITION PRODUCED BY 10-6 MOL D-TUBOCURARINE IN ISOLATED PHRENIC NERVE HEMIDIAPHRAGM PREPN FROM RATS.|THE BETA-OXIDATION RATE OF DODECANEDIOIC ACID IN RAT LIVER HOMOGENATES WAS DETERMINED BY SIMULTANEOUS MEASUREMENTS OF THE C6-C12 DICARBOXYLIC ACID IN RELATION TO TIME IN ASSAYS INCUBATED WITH DODECANEDIOIC ACID. THE BETA-OXIDN RATE OF C8-C12-DICARBOXYLIC ACIDS WAS INCREASED MANY TIMES IN HOMOGENATES FROM CLOFIBRATE-TREATED RATS. 2.0 MMOL CYANIDE WAS UNABLE TO INHIBIT THE BETA-OXIDN RATE BUT CAUSED MINOR INCREASE IN THE RATE OF BETA-OXIDN IN HOMOGENATES FROM BOTH NORMAL & CLOFIBRATE-TREATED RATS. RESULTS STRONGLY INDICATE THE EXISTENCE OF A PEROXISOMAL BETA-OXIDN OF DICARBOXYLIC ACIDS.
Drug Information
DODECANEDIOIC ACID WAS ADDED TO DISPERSED CULTURES. HUMAN EPIDERMAL CELLS & MELANOCYTES WERE EXAMINED BY ELECTRON MICROSCOPY AFTER 7, 10, 15, & 30 DAYS. APART FROM A STIMULATION OF MELANOGENESIS, DICARBOXYLIC ACIDS CAUSED NO DETECTABLE DAMAGE TO MELANOCYTES, NOR DID THEY PREVENT GROWTH OF A 2ND GENERATION OF CELLS.
1,10-decanedicarboxylic acid
Dodecanedioic acid Use and Manufacturing
Induced mutation of dodecanedioic acid producing Candida tropicalis.
Adhesives and sealant chemicals
10,000,000 - 50,000,000 lb
All other chemical product and preparation manufacturing|Dodecanedioic acid: ACTIVE|DIBASIC ACID ESTERS ARE BETTER COSMETIC MATERIALS THAN CONVENTIONALLY USED LANOLIN OR PETROLATUM IN TERMS OF ODOR, COLOR, STABILITY, AND HOMOGENEITY.
Fatty Acyls [FA] -> Fatty Acids and Conjugates [FA01] -> Dicarboxylic acids [FA0117]
Computed Properties
Molecular Weight:230.30
XLogP3:3.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:11
Exact Mass:230.15180918
Monoisotopic Mass:230.15180918
Topological Polar Surface Area:74.6
Heavy Atom Count:16
Complexity:179
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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